Sophia Daum
Hannes Hagen
Erin Naismith
Dominik Wolf
Andreas Pircher- 1Internal Medicine V, Department of Hematology and Oncology, Medical University Innsbruck, Innsbruck, Austria
- 2Medical Clinic 3, Department of Oncology, Hematology, Immunoncology and Rheumatology, University Hospital Bonn (UKB), Bonn, Germany
Tumor progression depends primarily on vascular supply, which is facilitated by angiogenic activity within the malignant tissue. Non-small cell lung cancer (NSCLC) is a highly vascularized tumor, and inhibition of angiogenesis was projected to be a promising therapeutic approach. Over a decade ago, the first anti-angiogenic agents were approved for advanced stage NSCLC patients, however, they only produced a marginal clinical benefit. Explanations why anti-angiogenic therapies only show modest effects include the highly adaptive tumor microenvironment (TME) as well as the less understood characteristics of the tumor vasculature. Today, advanced methods of in-depth characterization of the NSCLC TME by single cell RNA sequencing (scRNA-Seq) and preclinical observations enable a detailed characterization of individual cancer landscapes, allowing new aspects for a more individualized inhibition of angiogenesis to be identified. Furthermore, the tumor vasculature itself is composed of several cellular subtypes, which closely interact with other cellular components of the TME, and show distinct biological functions such as immune regulation, proliferation, and organization of the extracellular matrix. With these new insights, combinational approaches including chemotherapy, anti- angiogenic and immunotherapy can be developed to yield a more target-oriented anti-tumor treatment in NSCLC. Recently, anti-angiogenic agents were also shown to induce the formation of high endothelial venules (HEVs), which are essential for the formation of tertiary lymphoid structures, and key components in triggering anti-tumor immunity. In this review, we will summarize the current knowledge of tumor-angiogenesis and corresponding anti-angiogenic therapies, as well as new aspects concerning characterization of tumor-associated vessels and the resulting new strategies for anti-angiogenic therapies and vessel inhibition in NSCLC. We will further discuss why anti-angiogenic therapies form an interesting backbone strategy for combinational therapies and how anti-angiogenic approaches could be further developed in a more personalized tumor-oriented fashion with focus on NSCLC.
Introduction
Angiogenesis is regulated by the balance of pro-angiogenic and anti-angiogenic factors present in a tissue, if vascular remodeling is required this balance shifts to an activating state, called the “angiogenic switch” (Bergers and Benjamin, 2003). In progressing tumors, a similar activated angiogenic phenotype occurs which promotes endothelial cell (EC) proliferation, migration, elongation and dissemination of metastases to distant organs (Teleanu et al., 2019). These findings proposed inhibiting angiogenesis as a highly potent anti-cancer therapeutical approach and have intensified the research for agents to hamper vessel formation in diverse tumors over the past decades (Augustine et al., 2019). Conclusively, inhibiting pro-angiogenic molecules including vascular endothelial growth factors (VEGFs) or their cognate receptors (VEGFRs), served as anti-angiogenic therapy approaches in advanced stage NSCLC patients, as well as other cancer entities, at the beginning of this century (Sandler et al., 2006) and reviewed in Jayson et al. (2016). High expectations for these anti-cancer drugs were shattered rapidly as they exhibited only marginal benefits in early clinical trials due to the acquisition of evasive or primary resistance mechanisms consequently leading to a transient therapy benefit. Therapy failure could be attributed to the interplay of adaptive mechanisms of the TME (e.g., eliciting compensatory angiogenic pathways) and its interacting cellular compartments including TECs. In the previous years, a more detailed characterization identified the (tumor) endothelium as a heterogeneous cell population with distinct functional and organ-specific phenotypes indicating multiple pathological features of the tumor vasculature (Rafii et al., 2016). In addition to tumor endothelial heterogeneity, other vessel formation processes alongside vascular sprouting, such as vessel co-option or vasculogenic mimicry (VM) were less acknowledged in NSCLC but may play an important role in anti-angiogenic therapy resistance. Furthermore, the ability of tumors to compensate for absent signaling molecules by activating alternative pathways represents another resistance mechanism. The inhibition of VEGF/VEGFR, for example, was shown to prompt tumors to sustain angiogenesis via the secretion of substitute factors such as PDGF (Crawford et al., 2009), bFGF (Babina and Turner, 2017) and angiopoietin-2 (Rigamonti et al., 2014), or by the recruitment of pro-angiogenic cells such as tryptase secreting mast cells (Wroblewski et al., 2017) thus, resisting single-target therapies. Previous studies using dual or multi-target antibodies which simultaneously inhibit several angiogenic signals exhibited an incremental anti-angiogenic efficacy in different tumor types (Li et al., 2016; Peterson et al., 2016; Liu et al., 2018; Hosaka et al., 2020). However, many processes and factors contributing to inefficacy and resistance to angiogenesis inhibitors, in particular those involving the tumor endothelium, remain ambiguous.
The transient combinational efficacy of anti-angiogenic agents and chemotherapy (in first-line, as well as in second-line therapy) could possibly be attributed to a “vascular normalization” phenotype. Nevertheless, the time window of vessel re-organization and normalization is not well understood in the clinical setting but could play a major role in the transmission of chemical agents directly to the tumor, thereby enhancing anti-cancer efficacy (Johnson et al., 2004; Sandler et al., 2006; Garon et al., 2014; Reck et al., 2014). Additionally, cancer immunotherapies which inhibit immune checkpoints (ICs) such as programmed cell death protein 1/programmed cell death 1 ligand 1 (PD1/PD-L1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA4) have become landmarks in cancer treatment. The interaction of tumor vasculature with immune cells has a severe impact on the responsiveness and immunodeficiency of the tumor. Vascular normalization due to VEGF-inhibiting therapy exhibited increased lymphocyte infiltration and T-cell activation which, combined with immune checkpoint inhibitors (ICI), elicited an improved anti-tumor immunity in preclinical trials (Allen et al., 2017; Schmittnaegel et al., 2017). Additionally, combinational therapy of anti-angiogenic agents and ICI resulted in the formation of HEVs, which enhances activation of circulating B- and T-cells by mediating migration into secondary lymphoid organs (Ager and May, 2015). When surrounded by dense B- and T-cell rich areas, HEV can further adapt to tertiary lymphoid structures (TLS) thereby triggering potent anti-tumor immunity, which can significantly improve patient outcomes (Martinet and Girard, 2013). We are confronted with a network of considerable aspects when it comes to anti-angiogenic therapy, many of which still require thorough investigation. Further characterization of the TME and the associated endothelium can help improve anti-angiogenic therapies and optimize the proposed powerful synergic efficacy of combinational therapeutical approaches in NSCLC.
The Role of Tumor Angiogenesis in NSCLC
Physiological angiogenesis has already been characterized in detail and previously reviewed elsewhere (Góth et al., 2003; Senger and Davis, 2011). The process of tumor angiogenesis, which occurs early during tumor progression, is similar to physiological vessel formation, but with differences in regulation and grade of activity (Hanahan and Folkman, 1996; Raica et al., 2009; Hanahan and Weinberg, 2011). Firstly, tumor associated ECs acquire a chronic activated state, the “angiogenic switch,” a result of the upregulation of angiogenic receptors and activation of the PI3K-AKT signaling axis (Phung et al., 2006). This activation results in increased proliferation, survival and migration, leading to distortion of the basement membrane as well as pericyte coverage in the tumor vasculature (Hida et al., 2016). Consequently, TECs exhibit dysregulated behavior and polarization resulting in leaky, hemorrhagic, and dysfunctional vessels. Thus, oxygen levels, nutrient availability and waste disposal is diminished, which has severe effects on the TME (Colegio et al., 2014; Sanctis et al., 2018). Furthermore, dysfunctional TECs severely impact lymphocyte adhesion, trafficking and migration to the local tissue, resulting in a highly immunosuppressive TME (Fridman et al., 2012).
Additionally, the tumor stroma, which consists of a mix of resident fibroblasts and pericytes as well as bone-marrow derived tumor infiltrating leukocytes (e.g., macrophages and mast cells), regulates angiogenesis. M2 polarized tumor associated macrophages can either directly activate angiogenesis by releasing VEGF, bFGF and PlGF or indirectly via the release of matrix-metalloproteinases (MMPs), which in turn remodel the extracellular matrix for an enhanced endothelial migration (Kessenbrock et al., 2010; Olson and Joyce, 2015). Fibroblasts, as well as myeloid derived suppressor cells (MDSCs) promote angiogenesis through expression of growth factors such as VEGF and bFGF (Shi et al., 2017). CSF-1, a cytokine crucial for the survival and differentiation of monocytes and macrophages, mediates the recruitment of MDSCs into the tumor niche, which in turn increases angiogenesis due to growth factor release (Shojaei et al., 2007). By blocking the CSF-1 signaling in combination with anti-VEGFR2 therapy, tumor growth could be markedly decreased in murine lung carcinoma models (Priceman et al., 2010). Mast cells comprise a major compartment of inflammatory cells present in the TME and exhibit important regulatory features regarding angiogenesis (Ribatti and Crivellato, 2012). Their granules contain various proteases, cytokines and growth factors including pro-angiogenic molecules such as VEGF, bFGF, PDGF and the potent angiogenic factor tryptase, which is released upon activation of IgE or c-kit receptors (Ribatti and Ranieri, 2015). Tryptase induces vascularization and vessel tube formation by stimulating proliferation of ECs and activation of MMPs (Ribatti and Crivellato, 2012). In NSCLC the number of tryptase positive MCs linearly correlates with microvascular density, confirming the important role of this enzyme in regulating tumor angiogenesis (Ibaraki et al., 2005; Carlini et al., 2010). Inhibition of c-kit and its ligand SCF could hamper mast cell infiltration into the TME, preventing degranulation and thereby producing a synergizing anti-angiogenic effect (Huang et al., 2008; Overed-Sayer et al., 2020).
Current vessel-inhibiting therapies for treating advanced NSCLC mainly focus on repressing the process of vessel sprouting predominantly triggered by VEGF signaling. In the past years, however, non-angiogenic processes in the TME have gained attention as they are suggested to significantly contribute to tumor progression while being resistant to traditional angiogenesis inhibitors. In highly vascularized organs such as the lung, it was observed that cancer cells start to grow along existing vessels to preserve access to essential nutrients and gases without the need to form new vasculature. This process is referred to as vessel co-option (Pezzella et al., 1997; Coelho et al., 2017). In contrast to the chaotic growth of angiogenic tumor vessels, co-opted vasculature remains well organized as deduced from normal tissues (Adighibe et al., 2006). So far, vessel co-option is suggested to result, at least in part, of differential mitochondrial metabolism, but it may also involve reduced inflammation (Donnem et al., 2013). The ECs of co-opted vessels experience severe molecular changes during this process, for e.g., starting to express angiopoietin-2, which results in strong regression of vessels in the tumor core (Coelho et al., 2017). Thereupon, the tumor core becomes hypoxic, which consequently activates the angiogenic switch in tumor vessels (Holash et al., 1999). In vitro studies of glioma cells suggest that tumor cells that facilitate vessel co-option are dependent on the endoplasmic reticulum based stress sensing protein IRE1 (Auf et al., 2010). Furthermore the MMP-activating protein B2R was shown to serve as a chemoattractant during the migration of glioma cells towards blood vessels (Montana and Sontheimer, 2011). Finally, CDC42, a protein involved in actin-dependent formation of cytoplasmatic extensions, together with CD44, a protein crucial for establishing cell-cell contact, enable the connection between tumor cells and vessel covering pericytes for vessel co-option (Caspani et al., 2014).
Another non-angiogenic mechanism termed “VM” describes the process where cancer cells gain endothelial abilities to form their own circulatory network consisting of microvascular tubes to preserve blood supply (Pinto et al., 2016). So far, the molecular mechanism behind VM is not yet understood, however, it appears that VE-cadherin, the most prominent receptor on ECs, may play an important role. VE-cadherin on tumor cells can activate PI3K through the ERK1/ERK2 pathway which subsequently activates the metalloproteases MMP14 and pro-MMP2, resulting in remodeling of the ECM to enable cancer cells to be reorganized into vessel-like tubes (Paulis et al., 2010; Delgado-Bellido et al., 2017). VM networks resemble embryonic vasculogenesis, referring to a highly aggressive tumor cell phenotype that converted to an embryonic-like, undifferentiated state to facilitate tube formation (Maniotis et al., 1999). Gene expression analysis of VM networks in aggressive melanoma identified genes correlated with various cellular phenotypes such as fibroblasts, ECs and epithelial cells (Bittner et al., 2000; Seftor et al., 2002a,b). Tumors positive for VM show an increased expression of the ECM component laminin5γ2 and several MMPs, underlining the importance of ECM remodeling for initiating and promoting this non-angiogenic process (Seftor et al., 2001). Furthermore, VM is associated with poor prognosis as it is mainly observed in aggressive forms of melanoma and lung metastases (Williamson et al., 2016). Taking the potent impact of these non-angiogenic processes in cancer progression into consideration, may help us explain the occurring resistance of lung tumors to VEGF-inhibitors (Döme et al., 2007; Bergers and Hanahan, 2008).
In summary, the pathological features of tumor-associated ECs and non-ECs which result in a complex cancer promoting TME are diverse, and consequently contribute to therapy failure of angiogenesis inhibitors as well as other therapy approaches in a remarkable fashion. To better understand the biological mechanisms behind drug resistance or lack of clinical benefit, further investigation into the detailed characterization of the endothelial compartment in the TME are essential.
Traditional Methods for Vessel Inhibition in NSCLC
Currently used anti-angiogenic agents have been developed and approved for clinical application after intense study of their molecular, cellular, and physiological mode of action using various experimental approaches. In the following part we summarize currently available methods for investigating tumor angiogenesis as well as anti-angiogenic agents that have already been accepted for treating NSCLC.
Methods to Study (Tumor) Angiogenesis
Experimental models remain the cornerstone for investigating tumor angiogenesis and the development of new anti-angiogenic therapies. As vessel sprouting is a multistep process there is a wide array of assays which enable individual evaluation of different stages, and each possesses specific advantages and disadvantages (Shahid et al., 2017; Stryker et al., 2019). To unravel these complex processes, it is crucial to understand the analytical potential of each model. In vitro methods represent the fundamental evaluation of tumor angiogenesis including basic functional analysis such as proliferation, migration, and tube formation. The big advantages of in vitro assays are their simplicity, high reproducibility, and cost effectiveness, while the disadvantages include the incomplete representation of the cellular heterogeneity and prevailing conditions present in human organs. Although findings from in vitro assays may never be conclusive alone, they serve as a preliminary projection of angiogenic processes upon treatment of choice and provide first insights into a testing hypothesis.
Ex vivo assays such as the thoracic aorta ring and retina angiogenesis methods represent the link between in vitro and in vivo analysis. Here, functional vasculature fragments of aorta/retina derived from mice or rats are immersed in a three-dimensional culturing system for evaluating vessel sprouting outgrowth under specific conditions. The advantage of this method over in vitro assays is the preservation of original EC properties within the tissue that are normally modified due to isolation processes and repeated passaging. The absence of blood flow and circulating EC progenitors or other factors constitute the main disadvantages of these methods.
For more accurate information regarding angiogenic processes upon treatment in a biological system or to perform long-term studies, in vivo methods are necessary. The most common systems to investigate angiogenesis in a living organism are the chicken chorioallantoic membrane (CAM) assay, matrigel plugs, and tumor xenograft models. CAM assays, which have already been in use for decades, utilize chorioallantoic membranes of fertilized chicken eggs to evaluate angiogenic processes. While this method is cost effective, highly reproducible and the outcomes are easily visualized, it must be taken into consideration that vessel growth is evaluated during developmental stages, which can affect studies investigating mechanisms in mature vasculature. Matrigel plug assays enable the use of an in vitro tool in an in vivo setting. Here, vascular growth is evaluated by injection of matrigel, a synthesized substrate resembling basement membrane matrix, into an animal model which allows easy stimulation, subsequent excision, and investigation of the plug with, for example, immunohistological stainings. Compared with CAM assays, the matrigel plug can be used in more analytical methods and provides a fast and reliable representation of angiogenic processes in a biological system. Nevertheless, this method may require more replicates due to higher variability of results and is therefore more expensive. Lastly, transplantation xenografts represent the most advanced method to investigate tumor angiogenesis in a living organism. Tumor cells, mostly of human origin, are injected into immunodeficient mice to induce formation of a cancer mass that can be further treated and monitored for changes regarding tumor angiogenesis. This method most suitably reflects the pathological mechanism of vessel growth in vivo in the presence of blood circulation, as well as diverse environmental factors. Furthermore, it enables the long-term study of diverse processes associated with angiogenesis that are observed in a biological system such as tissue invasion, distant metastasis formation as well as non-angiogenic processes like vessel co-option and VM, which are known to promote resistance mechanisms in various cancers. Aside from the ethical aspect, a considerable disadvantage of this method is the incomplete or lacking representation of the immune system due to immunosuppression of the study organism.
Examining which experimental assay is most suitable for investigating a chosen angiogenic process under certain conditions, necessitates extensive deliberation with the desired endpoint, required technical equipment, level of experimental throughput, cost, and ethics kept in mind. Additionally, the complexity of angiogenesis cannot be unraveled using a single analytical method but the thought-out application of multiple overlapping analyses, ranging from cellular to physiological levels, are necessary to obtain robust findings worth testing in the clinical setting.
Anti-angiogenic Therapies Approved for Treating NSCLC
In 2004, the first VEGFA-inhibiting antibody, bevacizumab, was approved for use in advanced colorectal cancer in combination with chemotherapy and was followed in 2006 in NSCLC (Sandler et al., 2006). Since then, diverse anti-angiogenic antibodies or tyrosine kinase inhibitors (TKIs) have been developed, which block either VEGF-A binding to the receptor or directly inhibit VEGFR-2 to hamper vascularization in tumors. VEGF-pathway inhibition has a broad anti-angiogenic effect in tumors: (1) it primarily inhibits vessel growth which induces regional cancer cell death and delays progression of the tumor rather than diminishing its size (Escudier et al., 2007); (2) it induces EC apoptosis as VEGF acts as a survival factor on the endothelium by activating BCL2, Akt signaling, or apoptosis inhibitors (Gerber et al., 1998; Fujio and Walsh, 1999); (3) it blocks the recruitment of hematopoietic or endothelial progenitor cells for new vessel formation which provides an essential function in neovascularization in growing tumors (Rafii et al., 2002; Bertolini et al., 2006). Angiogenesis inhibitors in combination with either chemotherapeutics, targeted therapies or ICI, in first or second-line therapies in NSCLC, have exhibited improved efficacy and feasible safety, which significantly improved response rates and prolonged progression free survival (PFS) in a large number of patients. Currently three anti-angiogenic agents, namely bevacizumab, ramucirumab and nintedanib are FDA/EMA approved for use in advanced stage NSCLC and are summarized in Table 1 (Hall et al., 2015; Alshangiti et al., 2018; Janning and Loges, 2018) while more are in clinical testing. Despite the remarkable clinical benefits of these combinational approaches on response rate and PFS, the overall survival (OS) benefits were modest due to acquired drug resistance. It is important to mention that in most lung cancer studies anti-angiogenic therapy is administered until the onset of severe drug related adverse effects or disease progression. So far, there is only preclinical evidence that discontinued angiogenesis inhibition results in TME reorganization and perhaps causes a rebound effect of tumor angiogenesis. In tumor and healthy mouse models, it could be shown that anti-VEGF therapy withdrawal resulted in rapid tissue revascularization and long lasting structural changes including vessel hyper-permeability and increased metastasis in the diseased cohort (Yang et al., 2016). The treatment-triggered hypoxia which induces angiogenesis especially during therapy-withdrawal is one possible explanation to this tumor promoting off-drug effect. The benefit of continuous anti-angiogenic therapy beyond disease progression in the clinical setting was first analyzed in a phase 3b trail in 2018 which included 485 advanced NSCLC patients (Gridelli et al., 2018). Here, bevacizumab was administered in addition to standard of care therapy beyond disease progression. While, the treatment continuation of bevacizumab yielded no substantial therapy benefit, improvements in efficacy, and no new safety signals were observed. Based on these findings, the approach of continuous angiogenesis inhibition should be further investigated but may be recommended at a certain degree in the future. Nevertheless, treatment decisions should be based on individual therapeutic efficacy, which needs to be tracked throughout the entire therapy. However, the absence of reliable biomarkers with predictive features for anti-angiogenic therapies hamper further therapy improvement, thus molecular screening for markers associated with tumor angiogenesis is currently of great value.
Table 1. Clinical studies of anti-angiogenesis based therapies in NSCLC that led to FDA/EMA approval.
New Molecular Candidates to Predict and Track Anti-Angiogenic Efficacy in NSCLC
As previously mentioned, there is a great need for biomarkers to predict and track anti-angiogenic therapy efficacy, to help overcome innate and acquired resistance as it is still the main obstacle that restrains clinical success (Bergers and Hanahan, 2008). So far, predictive angiogenesis-associated biomarkers in NSCLC are lacking, highlighting the need for further investigation to improve this anti-tumor approach.
In a recent study, it was demonstrated that immunohistochemically confirmed TTF-1 expression in advanced non-squamous NSCLC samples, which is a known prognostic biomarker of lung adenocarcinomas, could be linked to therapy success of bevacizumab in combination with pemetrexed plus platinum derivatives (Takeuchi et al., 2018). TTF-1 positive tumors exhibited enhanced clinical benefits when bevacizumab was combined with the basic therapy whereas TTF-1 negative tumors did not benefit from this addition.
Furthermore, despite the previous results of the IMpower150 study, where significant clinical benefits of bevacizumab in combination with ICI and chemotherapy were shown, regardless of PDL-L1 expression, a phase 1b study by Herbst et al. observed contrary results. They reported a beneficial efficacy of ramucirumab in combination with the PD-L1 inhibitor pembrolizumab especially in patients with a PD-L1 expression above 50% (Herbst et al., 2019). According to this, PD-L1 expression remains a predictive marker of ICI therapy or ICI therapy in combination with anti-angiogenesis agents in NSCLC. Qiu et al. recently examined the benefit of anti-angiogenic therapies (bevacizumab, anlotinib or others) with anti-PD-L1 agents (nivolumab or pembrolizumab) in a real-world study including 69 NSCLC patients. Subgroup analyses in the cohort revealed that the response and PFS of this combinational therapy was significantly higher when it was administered as first-line therapy compared to other lines of treatment, and when the therapy was initiated within the first 6 months of diagnosis compared to later time points (Qiu et al., 2020). Additionally, patients with EGFR wildtype tumors exhibited significantly prolonged PFS after the combinational therapy compared to patients with EGFR mutated tumors. Interestingly, no correlation between PDL-1 expression levels and the efficacy of this combinational therapy has been observed so far, however, follow up will be continued. In short, these study results can help to optimize the use of anti-angiogenic agents in combination with PD-L1 inhibitors, however, more factors need to be investigated to yield an optimal benefit.
Another potent multi-targeted anti-angiogenic TKI, anlotinib, has already shown profound benefits as third-line combinational therapy in advanced NSCLC (Han et al., 2018a,b). A transcriptomics study of an anlotinib-resistant lung cancer cell line, indicated that CXCL2, a cytokine involved in wound healing and angiogenesis, was also involved in anlotinib-resistance (Lu et al., 2019a). In vitro assays demonstrated that exogenous CXCL2 could recover anti-angiogenic-induced inhibition of migration and invasion and prevent apoptosis of anlotinib-resistant cells. Furthermore, in a retrospective analysis, anlotinib-induced decrease of the inflammatory cytokine CCL2 in serum correlated with prolonged PFS and OS (Lu et al., 2019b). Nevertheless, resistance and poor response to anlotinib hinder drug efficacy. While the underlying mechanisms are still unknown, elevated serum-levels of two angiogenesis-related markers KLK5 and L1CAM were recently correlated with poor response to anlotinib (Lu et al., 2019b).
Easily available predictive biomarkers, e.g., liquid biopsy, which allow the continuous track of response to angiogenesis inhibition are highly desired to optimize efficacy, as most of the current methods involve invasive procedures (biopsy or surgery) which limit analytical accessibility.
Several studies suggested a potential prognostic value of VEGF in NSCLC but so far investigations into circulating VEGF levels have not yielded consistent results (Rodríguez Garzotto et al., 2016). In the E4599 study, high VEGF levels in pretreatment plasma of 878 patients with advanced stage NSCLC, who received combinational treatment of bevacizumab plus chemotherapy, correlated with increased overall response but had no predictive outcome on survival (Dowlati et al., 2008). Another study observed contrary results when baseline plasma biomarkers of 303 non-squamous NSCLC patients undergoing similar therapy were evaluated (Mok et al., 2014). Here, baseline VEGFA levels in the plasma correlated with prolonged PFS and OS but showed no association with response rates to the therapy. The predictive value of VEGF or other proangiogenic factors on anti-angiogenic drug response is a highly discussed matter revealing vastly variable results. This is partly due to analytical variability, including sample collection and handling, as well as the disagreements regarding the most suitable sample choice for evaluating circulating factors (Rodríguez Garzotto et al., 2016). For example, serum or platelet rich plasma may not adequately represent the physiological VEGF level as it has been shown that the clotting processes initiates VEGF release in platelets (Webb et al., 1998). Moreover, the pathological situation can impact VEGF levels, as patients with more advanced tumors or several metastatic tumor sites exhibit a higher baseline level of plasma VEGFA, suggesting that VEGFA is linked to the tumor burden (Mok et al., 2014). Previously proposed correlations of circulating angiogenic factor levels with anti-angiogenic therapy efficacy in lung cancer seem to reflect tumor biology thus, have an important prognostic role rather than to be predictive (Crohns et al., 2010). The observed trend of increasing circulating factors in response to angiogenesis inhibition on one hand was shown to depend considerably on the TME and may represent therapy-induced hypoxia (Zaman et al., 2006; Kut et al., 2007). On the other hand, high VEGFA levels could also be attributed to TP53 mutated lung tumors which correlated with improved efficacy of bevacizumab (Schwaederlé et al., 2015). A currently identified alternative biomarker for bevacizumab-based chemotherapy combinations in patients with advanced NSCLC is CXCL16. In the analyzed sera of 40 advanced staged NSCLC patients therapy-induced decrease of CXCL16 levels correlated with prolonged OS compared with patients exhibiting only moderate decrement (Shibata et al., 2020).
However, confirming if any of these molecular markers indeed exhibit adequate predictive features necessitates further investigation. New aspects of processes which promote tumor angiogenesis, and a better understanding of the endothelium as driving force can help identify reliable biomarkers and overcome therapy failure in NSCLC.
Mechanisms of Tumor Vascularization in NSCLC
There are several mechanisms on both the cellular and environmental levels which can promote vessel formation in human tumors, many of which are not yet been completely elucidated. Although angiogenesis may represent the most important part of tumor vascularization, other processes that result in perfusion of the tumor tissue should be investigated in more detail and considered when designing new anti-angiogenic approaches in NSCLC.
In the following part we summarize various levels of tumor vascularization that may represent new targets for vessel inhibition in NSCLC. All mentioned mechanisms are summarized in Figure 1.
Figure 1. Mechanisms of tumor vascularization in NSCLC. Tumor vascularization in lung cancer can be promoted by various processes which overlap during cancer progression. In general tumor vascularization/angiogenesis can be stimulated on the cellular level (TEC properties), the environmental level (TME stimuli) or facilitated in absence of angiogenic signaling (non-angiogenic processes). TECs exhibit upregulated metabolism to enable high angiogenic activity which includes processes involved in proliferation (cholesterol synthesis and glycolysis) and processes that enable migration via ECM remodeling (collagen synthesis). Potential targets involved in these pathways (SQLE, PFKFB3, and ALDH18A1, respectively) are considered to increase the angiogenic potential of TECs in NSCLC. Hypoxia and acidosis induced by high levels of lactate due to upregulated glycolysis constitute to a highly pro-angiogenic tumor environment. Angiogenesis stimulating factors (VEGF, bFGF, PDGF, HIF-1α, tryptase, and MMPs) are released by both, cancer cells and stromal cells, including fibroblasts, pericytes, tumor associated macrophages and ECs. Non-angiogenic processes constitute to tumor vascularization and are inaccessible for anti-angiogenic agents, thus contributing to therapy resistance. VM comprises the formation of tubular structures arising from cancer cells that gain endothelial like properties to maintain vascular supply during cancer progression. Another mechanism of cancer cells to persist in circulation is to grow along existing vasculature, which is referred to as vessel co-option. In this figure we summarized the various mechanism of tumor vascularization that should be considered when targeting the inhibition of tumor vessels in NSCLC.
TEC Characteristics That Promote Tumor Vascularization in NSCLC
The endothelium is postulated to be a large contributor to the therapeutic efficacy of anti-angiogenic therapies, and therefore represents a possible source of therapy response or failure. It is well known that the process of angiogenesis is comprised of different EC phenotypes which execute distinct functions. During the elongation of the sprouting vessel VEGF-sensitive tip ECs migrate into avascular tissue regions, thus leading the proliferating trailing stalk ECs, which built up the growing vessel. Newly formed vasculature finally adapts a mature and quiescent phenotype referred to as phalanx ECs (Carmeliet and Jain, 2011; Betz et al., 2016). The EC phenotypes involved are highly dynamic and can reprogram the gene expression to meet their current physiological requirements. However, the tumor endothelium was not studied in depth and a recent single-cell RNA sequencing (scRNA-Seq) study identified even more EC phenotypes from both healthy and tumor tissue from lung cancer samples as already known, indicating a much more complex phenotypic heterogeneity of the (tumor) vasculature than initially presumed (Goveia et al., 2020). Interestingly, although phenotype proportions differed strongly between analyzed NSCLC patients, they collectively observed a low abundance of tip and proliferating TECs, which represent the main targets of traditional anti-angiogenic therapy. Furthermore, they identified a so-far-unknown tumor exclusive phenotype of activated postcapillary vein EC that upregulated features known from HEVs in inflamed tissues such as immunomodulatory factors and ribosomal proteins. The unexpected finding that activated and proliferating TECs only represent a minority of the pathological EC phenotypes found in NSCLC, allows us to reconsider currently used anti-angiogenic therapy as less of a vessel-inhibiting strategy, and more of a strategy to modulate the higher proportion of mature TECs into potent participants of tumor surveillance.
In order to develop new angiogenesis-inhibiting therapies, the molecular differences between physiological and pathological ECs will need to be elaborated. Genetically TEC and NEC phenotypes significantly differ in gene expression affecting diverse cellular mechanisms such as proliferation, migration, inflammation, and angiogenesis (Figure 2). Previous studies have shown that one key feature of TECs is a highly active metabolism, which permits pathological processes as increased proliferation and angiogenesis (Cantelmo et al., 2016). TECs exhibit upregulated glycolysis due to elevated expression of 6-phosphofructo-2-kinase/fructose-2,6-biphosphatase 3 (PFKFB3), which regulates proliferation and migration during tumor angiogenesis (van der Veldt et al., 2012; de Bock et al., 2013). Hyperglycolytic TECs subsequently release high amounts of lactate into the environment, which in turn, further stimulates EC proliferation and angiogenesis (Annan et al., 2019). It could be demonstrated that inhibition of PFKFB3 resulted in improved drug efficacy and decreased metastatic events in tumor mouse models (Cantelmo et al., 2016). Another study in xenograft NSCLC mouse models exhibited that PFKFB3 mRNA silencing in combination with docetaxel results in a chemoenhancing effect and increases anti-cancer efficacy compared with monotherapies alone (Chowdhury et al., 2017). Furthermore, to sustain upregulated proliferative capacity, TECs exhibit elevated nucleotide biosynthesis including upstream pathways that are involved in serine and lipid synthesis (Cantelmo et al., 2016; Bruning et al., 2018; Li et al., 2019). In addition, Lambrechts et al. (2018) showed that MYC-targets, which are involved in transcription processes, were most upregulated in TECs of human NSCLC samples. Interestingly, c-MYC expression induces angiogenesis in combination with HIF-1α and VEGF (Lee and Wu, 2015) and recruits tryptase positive mast cells into the tumor niche (Soucek et al., 2007), therefore, MYC inhibition may have a potential anti-cancer effect.
Figure 2. The multifaced picture of TECs in NSCLC. TECs possess features that enable continuous angiogenic activity for progressing vascularization of the tumor. These features are ensured by genetical changes in the tumor endothelium that are triggered by diverse stimuli of the TME e.g., hypoxia and growth factor release. The stroma, consisting of various cells, promote angiogenesis by directly releasing signaling molecules into the adjacent tissue, thereby stimulating TECs. Fibroblasts and myeloid derived suppressor cells (MDSCs) activate angiogenesis by releasing VEGF and bFGF into the TME. Additionally, CSF-1 molecules, expressed by cancer cells, further recruit MDSCs into the tumor niche. Tumor associated macrophages (TAMs) can directly induce angiogenesis by releasing VEGF, bFGF, and PlGF, or indirectly by releasing matrix metalloproteinases (MMPs) which promote endothelial migration. Mast cells secrete tryptase (TRYPT) into the TME which stimulates EC proliferation and enables ECM remodeling. Furthermore, to facilitate enhanced angiogenesis, TECs upregulate the surface expression of angiogenic receptors as well as increase metabolic activity including energy and amino acid metabolism and the biosynthesis of nucleotides. In addition to the high angiogenic activity, TECs can directly suppress inflammatory responses by downregulation of inflammatory cytokines for immune cell recruitment (CCL2, CCL8, and IL-6), receptors required for immune cell homing (ICAM) or lymphocyte activation (MHC I and MHC II) which results in impaired immune cell trafficking and migration into the TME. In summary the complex interaction of tumor-protecting environmental conditions and the pathological features of TECs lead to a pro-angiogenic and immune suppressive TME in NSCLC.
Focusing on endothelial metabolism in cancer, a recent study could identify at least two metabolic signatures which are highly upregulated in angiogenic endothelium and TECs. One for proliferation, which includes gene sets associated with biomass production e.g., glycolysis, TCA cycle, fatty acid oxidation, cholesterol biosynthesis and amino acid metabolism, and one for remodeling of the extracellular matrix including gene sets for collagen biosynthesis in particular proline synthesis (Rohlenova et al., 2020). These results educed two new possible metabolic targets to hamper tumor angiogenesis; aldehyde dehydrogenase 18 family member A1 (ALDH18A1), an enzyme essential for de novo biosynthesis of proline; and squalene epoxidase (SQLE), the rate-limiting enzyme in cholesterol biosynthesis. Silencing of ALDH18A as well as SQLE impaired EC proliferation, migration and vessel sprouting in in vitro assays. Summarized, targeting endothelial metabolism in cancer is an interesting therapeutic option that could possibly assist an anti-angiogenic approach for treating NSCLC.
Another key feature of TECs in lung cancer is the downregulation of inflammatory responses thus contributing to tumor-associated immune escape. Single-cell analysis of NSCLC samples identified the most downregulated genes of the tumor endothelium in connection to inflammation, which included CCL2, CCL18, and IL6, essential for immune cell recruitment; MHC I and II, essential for immune cell activation; and ICAM, required for immune cell homing (Lambrechts et al., 2018). As the endothelium represents the primary connection between the immune system and tumor cells, these results indicate the important role of TECs in immunomodulatory processes that hamper anti-tumor immunity. It has been demonstrated that angiogenesis inhibition can restore proinflammatory surface proteins on TECs during a therapy-induced process termed “vessel normalization” (Goveia et al., 2020). Vessel normalization not only improves immune cell activation and infiltration, but is also suggested to enhance drug delivery to the tumor sites, thus improving its efficacy (Allen et al., 2017; Schmittnaegel et al., 2017). Additionally, combinational therapy of angiogenesis inhibitors and immunotherapy (anti-PD-L1) in previous studies could elicit the formation of unique blood vessels in treated tumors that resemble HEVs typically found in lymphoid tissues, which implicated increased treatment efficacy (Allen et al., 2017; Schmittnaegel et al., 2017). HEVs can mediate immune cell adhesion and migration into the tumor, which may be important for bypassing TEC-induced immune escape (Ager and May, 2015). In the already discussed scRNA-Seq study by Goveia et al., they demonstrated that VEGFR inhibition could induce vessel normalization by shifting invasive, low immunogenic TEC phenotypes to a more quiescent, immune-modulatory phenotype resembling HEVs (Goveia et al., 2020). These remarkable observations indicate that TECs comprise the ability to transform into HEVs to promote immune cell infiltration into the tumor and induce a potent anti-tumor response. This extends the previous observations of favorable synergistic effects of immune therapy in combination with angiogenesis inhibitors in NSCLC, especially when it results in HEV formation. Furthermore, direct induction of HEV formation could be a promising new strategy in anti-angiogenic approaches that may attain great clinical importance. However, currently there are no reliable biomarkers to track the process of vessel normalization or HEV formation in NSCLC which could help to predict and optimize this new treatment strategy.
Non-angiogenic Mechanisms in Association With Neovessel Inhibition in NSCL
As mentioned above, in some cases tumor vascularization can be facilitated by non-ECs which adapt certain properties to sustain access to the circulation, which may support anti-angiogenic drug resistance. During tumor progression, processes that lead to vascularization of the malignant tissue can vary locally as well as temporarily and involve angiogenic as well as non-angiogenic mechanisms even in the same lesion (Bridgeman et al., 2017). In lung tumors, where non-angiogenic tumor growth occurs most commonly, previous studies primarily located non-angiogenic processes in the tumor periphery, whereas angiogenesis is typically localized in the hypoxic tumor core (Pezzella et al., 1997; Donnem et al., 2018). Here, we briefly discuss the impact of non-angiogenic processes in NSCLC on anti-angiogenic drug efficacy based on previous studies.
VEGF-A inhibition using bevacizumab failed to inhibit VM in breast cancer cells in vitro, furthermore, sunitinib, a multi targeting anti-VEGFR inhibitor, even promoted VM in breast cancer mouse models (Dey et al., 2015; Sun et al., 2017). Additionally it could be demonstrated that VM in NSCLC depends on expression of Sema4D and its receptor plexinB1 which activate RhoA and downstream ROCK, comprising an already known angiogenesis-promoting process in tumors (Basile et al., 2006). Inhibition of Sema4D or downregulation of plexinB1 resulted in RhoA/ROCK pathway inhibition and could reduce VM formation in human NSCLC cell lines (Xia et al., 2019). Although the role of VM in NSCLC is not fully understood, previous observations suggest that it may contribute to anti-angiogenic therapy failure and may serve as an option to treat aggressive lung tumors.
Vessel co-option on the other hand is a common phenomenon especially observed in lung metastases when tumor cells start to invade perivascular tissues (Jensen, 2016). Anti-angiogenic therapy with sunitinib could induce a switch from angiogenic vessel formation to vessel co-option in a lung metastatic mouse model, which ultimately resulted in sunitinib resistance (Bridgeman et al., 2017). Unfortunately, regulative mechanisms of vessel co-option in human tumors remain unknown in large part, however, predicting the occurrence of either VM or vessel co-option could be a useful tactic to prevent anti-angiogenic drug resistance in some patients. According to these and other results, it could be confirmed that non-angiogenic tumors contribute to anti-angiogenic therapy resistance which reveals the undoubted importance of targeting both angiogenic, but also non-angiogenic vessel growth to treat NSCLC (Donnem et al., 2018).
New Aspects for Vessel Inhibition in NSCLC
Increasing knowledge of the physiological processes of tumor vascularization in addition to traditional angiogenesis has enlightened a variety of adaptive mechanisms which can promote anti-angiogenic therapy resistances. This awareness fortifies the necessity for alternative anti-angiogenic agents besides traditional anti-VEGF therapy.
New Targets for Vessel Inhibition in NSCLC
As previously examined, tumor angiogenesis depends on upregulated metabolic activity e.g., elevated cholesterol levels in TECs. Cholesterol not only represents a fundamental structural component of cell membranes and serves as precursor for several steroid hormones, it is also crucial for membrane function and angiogenic signaling, making it a favorable target for tumor vessel inhibition (Lyu et al., 2017). Inhibition of intracellular cholesterol trafficking with anti-inflammatory drug chepharantine was shown to hamper angiogenesis and tumor growth in lung cancer xenograft mice while improving anti-tumor activity of standard chemotherapeutics (Lyu et al., 2017). Another study has shown that pharmacological lowering of intracellular cholesterol levels with pitavastatin could reduce growth and migration and induced apoptosis in human lung tumor-associated ECs in vitro (Hu et al., 2020). In vivo experiments using lung cancer xenograft mice exhibited that pitavastatin-treatment could completely arrest tumor growth in these animals when combined with cisplatin and delayed tumor growth and impaired angiogenesis in cisplatin-resistant mouse models.
Another potential angiogenic target for cancer treatment is tie1. While the second tie receptor, tie2, is well characterized as a regulator during late stages of angiogenesis (e.g. vascular maturation or in quiescent ECs) via the angiopoetin/tie signaling pathway, an associated ligand for the less studied tie1, has not yet been identified (Augustin et al., 2009). In contrast to tie2, tie1 is upregulated in angiogenic vessels and downregulated in quiescent ECs and is somehow involved in the regulation of the angiopoietin/tie signaling cascade (Sato et al., 1995; Kim et al., 2016; Korhonen et al., 2016; La Porta et al., 2018). As tie1 is also upregulated in intratumoral vasculature, its deletion on ECs successfully produced a potent anti-angiogenic effect in different cancers (Kaipainen et al., 1994; Aguayo et al., 2001). In fact, EC-specific deletion of tie1 in lung carcinoma and melanoma mouse models resulted in delayed cancer growth, predominantly in late-stage tumors (La Porta et al., 2018). Furthermore, it inhibited neovessel sprouting and a reduced intratumoral vessel density, while the remaining mature vasculature became strongly normalized, which limited further metastatic formation. These findings, and the fact that tie1 expression is increased in angiogenic endothelium compared with resting vasculature, presents tie1 as a highly potent angiogenic target, especially in the treatment of advanced staged NSCLC.
Another considerable strategy of anti-angiogenic therapy could include targeting micro RNAs (miRNAs) as they represent a new paradigm in molecular cancer therapy. The impact of miRNAs in post-transcriptional regulation has already been associated with pathways involved in cancer and vascular disease as summarized in Sun et al., 2018. The following studies evaluated the potential role of specific angiogenesis-related miRNAs as targets in lung cancer. Hsu et al. observed that miR-23a, a micro RNA known to be hypoxia-associated, was overexpressed in exosomes of oxygen depleted CL1-5 lung cancer cells (Hsu et al., 2017). Furthermore, these cancer-cell derived exosomes could induce angiogenesis via HIF-1α signaling in vitro when internalized by HUVECs. Additionally, miR-23a transfection increased permeability and transendothelial migration of cancer cells in vitro by downregulation of the tight junction protein ZO-1 and stimulated neovascularization and tumor growth in vivo in CL1-5 xenograft mice, proposing it to be an appealing target for anti-angiogenic therapy. Upregulation of miR-195 in squamous lung cancer cells in vitro on the other hand could be associated with impaired VEGF expression and hampered migration and invasion, thereby facilitating a tumor-suppressive function. Additionally, overexpression of miR-195 in HUVECs was observed to inhibit tube formation and reduced the expression of VEGF, which hampered their angiogenesis activity in vitro (Liu et al., 2019).
As it is an essential process during vessel growth, targeting ECM remodeling may also be an interesting approach to inhibit tumor angiogenesis in NSCLC. The most prominent enzymes involved in this process are matrix-metalloporoteinases (MMPs) which are inhibited under physiological conditions by tissue inhibitors of metalloproteinases (TIMPs). miR-130b could be identified as a promotor of MMP-2 activity and invasion of NSCLC cancer cells in vitro by downregulation of TIMP-2. Additionally, it could be observed that miR-130b was significantly upregulated in tumor tissue of NSCLC patients with vascular cancer cell invasion (Hirono et al., 2019). According to these findings, targeting miR-130b could be a strategy to impede angiogenesis and cancer cell invasion in lung cancer.
Uribesalgo et al. suggested targeting the apelin signaling pathway to inhibit tumor vessel formation in lung cancer (Uribesalgo et al., 2019). Apelin is a conserved peptide involved in developmental angiogenesis and is also upregulated in ECs within the TME. Previous studies could associate high apelin levels with a poor clinical outcome in patients with NSCLC (Györffy et al., 2010). In murine lung cancer models, apelin knockout reduced tumor burden and prolonged survival by inhibiting VEGF, TGF-β1, and TNF-α and simultaneously decreased MDSC infiltration in the TME (Uribesalgo et al., 2019). The combination of pharmacological inhibition of apelin with the anti-angiogenic drug sunitinib in lung cancer and mammary cancer mouse models, significantly delayed tumor growth and could almost double the survival, even in the KRAS driven or p53 mutated tumors, when compared with sunitinib treatment alone. Finally, apelin loss also reduced vessel density and prevented sunitinib-induced hypoxia and poor vessel structure in the TME. Conclusively, apelin inhibition may provide a potent synergistic anti-tumor effect when combined with anti-angiogenic agents, while, and most importantly, avoiding therapy-induced hypoxia of the TME, thus decreasing the chance of metastases, and bypassing potential therapy resistances.
New Therapy Approaches for Vessel Inhibition in NSCLC
Single-target anti-angiogenic agents have already shown their limitations in clinical settings (Jayson et al., 2016). Even in combination with other therapy approaches like standard chemotherapy or immune therapy, treatment success remains largely marginal. Targeting several pro-angiogenic molecules with recombinant fusion proteins could therefore increase the anti-angiogenic effect of such therapies. Zhang et al. (2020) could successfully establish a multi-epitope peptibody containing bFGF and VEGF sequences, which could provoke a potent anti-bFGF/VEGF response by inhibiting proliferation and migration of lung cancer cells as well as HUVECs in vitro. When injected into lung cancer mouse models, autologous generated anti-peptibody antibodies inhibited tumor progression and angiogenesis and decreased expression of bFGF, VEGFA and PDGF in the tumor tissue. Targeting angiogenesis with fusion proteins exhibited potent anti-tumor efficacy in murine models and may represent a new approach for vessel inhibition in NSCLC, especially in combination with other therapy agents aimed at important angiogenic factors, previously discussed potential TEC specific markers or cellular mechanisms (Table 2).
Table 2. Pro-angiogenic factors involved in angiogenesis.
The instability of tumor vessels due to morphological abnormalities (e.g., incomplete pericyte coverage) impedes drug delivery to the local lesion. Although anti-angiogenic therapy can temporarily restore tissue perfusion and drug delivery by vascular normalization, treatment withdrawal often results in vessel hyper-permeability and can even induce a rebound effect of tumor angiogenesis (Yang et al., 2016). As continuous inhibition of angiogenesis remains difficult to implement for health or economic reasons, an alternative or more independent delivery system of anti-angiogenic agents could help to overcome these issues. Nanomaterials have become an emerging field in cancer therapy in recent years, as their unique molecular properties make them suitable targeted drug delivery-systems. Physiochemically, these nanoparticles match the size of inter-endothelial junctions of blood vessels in the TME and therefore increase permeation and retention (EPR) resulting in a passive drug delivery (Chauhan and Jain, 2013). Nanomaterials such as liposomes or nanotube carbon structures are used to deliver anti-angiogenic agents and improve drug specificity while reducing cytotoxic side effects, drug clearance and resistance mechanisms in the treatment of NSCLC (Seshadri and Ramamurthi, 2018). In the past, studies using biodegradable polymers as nanocarriers to deliver chemotherapeutics and targeted drugs exhibited significant anti-tumor efficacy in vitro and in vivo. For example, paclitaxel encapsulated aldehyde polyethylene glycol-polylactide (PEG-PLGA) conjugated to a VEGFR2-inhibiting peptide showed increased internalization in HUVECs in vitro as well as potent activity against breast cancer models in vivo (Yu et al., 2010). Although there are several peptide motifs that are suggested to target tumor endothelium such as RGD or NGR which can bind integrin heterodimers CD51 and CD61, or aminopeptidase N, respectively, their targeting with nanomaterial is not yet applied for treating NSCLC (Sakurai et al., 2019). Furthermore, non-angiogenic mechanisms such as VM or vessel co-option could also represent possible targets for nanomaterial-based therapy as the EPR effect of such molecules could help to overcome delivery and infiltration issues of traditional cancer therapeutics. However, nanotherapeutics may provide a new potential anti-angiogenic therapeutical approach, but as already discussed, there is still a need for more specific biomarkers to exclusively target tumor vasculature in an organ specific manner. Taking this into consideration, chimeric antigen receptor (CAR) T-cell therapy, which serves as personalized immune therapy using autologous T-lymphocytes, engineered to target specific antigens present in a tumor, could be used to exclusively eliminate TECs without damaging healthy vasculature. CAR T-cells already have shown remarkable clinical success in liquid malignancies like B-cell acute leukemia with response rates above 80%, however, this outstanding efficacy has not yet been translated into the solid tumor setting. The therapy failure can, at least in part, be attributed to the impaired accessibility of the tumor mass due to dysfunctional vasculature and immunosuppressive conditions in the TME. Targeting tumor vessels directly with CAR T-cells could therefore be a good strategy to overcome these issues, which at best, can normalize the defective vasculature and improve drug efficacy in combinational therapy settings. In a recent study Xie et al. (2019) generated VHH-based CAR T-cells targeting EIIIB, an alternatively spliced domain of fibronectin, which is strongly expressed during angiogenesis. Injected EIIIB-targeting CAR T-cells could delay tumor growth and improve survival in immunocompetent mouse models harboring aggressive melanoma, whereas colorectal cancer mouse models did not respond to the treatment. Here, the expression levels of EIIIB in the different tissues had impact on the therapy outcome which again highlights the importance of organ specific vascular markers as well as the impact of organ specific angiogenic activity when targeting tumor vessel formation. Other studies investigated the anti-angiogenic efficacy of TEM8-specific CAR T cells in solid cancer mouse models. TEM8 is one of the first discovered TEC markers and represents a promising target in anti-angiogenic therapy strategies (St Croix et al., 2000). In 2018, a study reported that TEM8-specific CAR T-cells could improve survival and significantly decreased vascularization in triple negative breast cancer mouse models and induced tumor regression in mice with lung metastases (Byrd et al., 2018). A more recent study, however, observed contrasting results where TEM8-sepcific CAR T-cells triggered high toxicity and induced inflammation in lung and spleen when injected into healthy mice (Petrovic et al., 2019). It is suggested that the engineered T-cells cross-reacted with other antigens or targeted TEM8 in healthy tissues, although it is normally expressed at a much lower quantity compared with pathological levels. However, both processes resulted in severe toxicity in vivo and again emphasize the need for more adequate, highly specific tumor-vessel exclusive markers that can be targeted with either CAR T-cells or other previously discussed inhibiting molecules.
So far, the main obstacles of anti-angiogenic therapy in NSCLC are evading- or intrinsic resistance mechanisms which still remain elusive. We have discussed a wide array of possible therapies and therapy systems that could improve anti-angiogenic efficacy when combined with standard treatment. The principal goal would be to expand the therapeutical effect of angiogenesis-inhibiting drugs on vessel normalization and render the tumor more vulnerable to additional agents such as chemotherapy or immunotherapy. In a recent study, Hosaka et al. could show that dual angiogenesis inhibition could sensitize resistant off-target tumors to therapy. Therefore they created mouse models of breast cancer or fibrosarcoma, both resistant to anti-VEGF and anti-PDGF treatment due to increased tumor associated expression of bFGF, a molecule which modulates the vasculature via pericyte recruitment in a PDGF-dependent process (Hosaka et al., 2020). Neither anti-VEGF nor anti-PDGF monotherapy had a significant anti-tumor effect on bFGF-positive tumors, but the combination of both agents produced a superior benefit, inhibiting cancer growth by suppressing proliferation and triggering apoptosis of tumor cells. Interestingly, even the pan-blocking of FGF-receptors did not yield a comparable benefit. To explain this unexpected effect, angiogenesis has to be considered as an interacting network of various signaling pathways which cannot be disrupted by blocking a single molecule. In this study the off-target anti-VEGF/PDGF therapy generated a synergistical effect in which PDGF inhibition ablated bFGF-dependent perivascular coverage which further sensitized tumor vessels to anti-VEGF inhibition. These findings demonstrate that the disruption of interacting angiogenic pathways by simultaneously targeting multiple angiogenic factors can provoke a highly potent anti-tumor effect which is able to circumvent mechanisms of therapy resistance, and thus should be considered as new approach to improve neovessel inhibition in cancer. While physiological, as well as pathological vascularization is comprised of diverse molecular pathways, several of which may serve as new targets, some in particular, such as VEGF/VEGFR signaling, represent key players of angiogenesis and should remain an irreplaceable anchor of anti-angiogenic therapy approaches in NSCLC.
Discussion
Angiogenesis is a main therapeutic concept in oncology, especially in NSCLC, where three approved agents are available in combination with chemotherapy or immunotherapy. Nevertheless, the therapeutic efficacy of the current anti-angiogenic therapies is not satisfying and needs a more personalized/individualized approach. Increasing knowledge in angiogenic processes and non-angiogenic processes that contribute to tumor vascularization, provide precise targets for novel therapy strategies and pave the way for developing new anti-angiogenic treatment concepts that target e.g., TEC metabolism, TEC specific factors, tumor vessel normalization and combinational approaches with CAR T-cells. These therapeutic concepts need to be evaluated for synergistic effects as, in our view, modern anti-angiogenesis represents the concept of shaping the TME rather than being a direct anti-tumor therapy itself. However, these therapeutic strategies are very promising in preclinical setting and the translation into a clinical setting is not only warranted but highly desired. Furthermore, a new horizon of targeted and functional TEC characterization was opened by scRNA-Seq studies, which proved that the tumor vasculature is highly heterogenous and differs from the normal adjacent vasculature more than primarily assumed in terms of metabolic activity, immune suppression and heterogeneity for example. In addition, new synergistic effects of TECs in their role of immunomodulation were identified and induction of HEV formation for immune priming is suggested to be a new therapeutic strategy. Next the organ specific context of the vasculature plays an important role and has to be further studied for better therapy allocation.
In conclusion the concept and goal of anti-angiogenesis in NSCLC in the future can be reshaped by abolishing the traditional vessel priming concept and moving toward a side specific molding of the TME, using the tumor vasculature as a tool, like a trojan horse.
Author Contributions
SD, HH, EN, AP, and DW developed the concept of the review. SD, HH, and EN drafted the review. DW and AP corrected and reviewed the review. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
The handling editor LT declared a past co-authorship with one of the authors AP.
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Keywords: non-small cell lung cancer, angiogenesis, vascular endothelial growth factor, tumor microenvironment, tumor endothelial cells, immunotherapy, combinational therapy
Citation: Daum S, Hagen H, Naismith E, Wolf D and Pircher A (2021) The Role of Anti-angiogenesis in the Treatment Landscape of Non-small Cell Lung Cancer – New Combinational Approaches and Strategies of Neovessel Inhibition. Front. Cell Dev. Biol. 8:610903. doi: 10.3389/fcell.2020.610903
Received: 27 September 2020; Accepted: 07 December 2020;
Published: 05 January 2021.
Edited by:
Lucas Treps, VIB KU Leuven Center for Cancer Biology, BelgiumReviewed by:
Anca Maria Cimpean, Victor Babes University of Medicine and Pharmacy, RomaniaGirolamo Ranieri, Istituto Nazionale dei Tumori (IRCCS), Italy
Patrycja Monika Nowak-Sliwinska, Université de Genève, Switzerland
Copyright © 2021 Daum, Hagen, Naismith, Wolf and Pircher. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Andreas Pircher, andreas.pircher@i-med.ac.at