Abdelhakim Salem
Elin Hadler-Olsen
Ahmed Al-Samadi- 1Department of Oral and Maxillofacial Diseases, Clinicum, Faculty of Medicine, University of Helsinki, Helsinki, Finland
- 2Translational Immunology Research Program (TRIMM), Research Program Unit (RPU), University of Helsinki, Helsinki, Finland
- 3Department of Medical Biology, Faculty of Health Sciences, UiT the Arctic University of Norway, Tromsø, Norway
- 4The Public Dental Health Service Competence Center of Northern Norway, Tromsø, Norway
Editorial on the Research Topic
Angiogenesis and Angiogenesis Inhibitors in Oral Cancer
This special issue of Frontiers in Oral Health sheds light on recent research regarding the tumor-related angiogenesis in oral cancer, including the present challenges of anticancer therapy targeting angiogenesis. Indeed, angiogenesis is a hallmark of solid tumors and it has important prognostic and therapeutic implications in cancer patients. This issue covers different relevant topics ranging from characterizing angiogenic signaling pathways to newly suggested paradigms of tumor neoangiogenesis revealing new putative therapeutic targets.
Oral squamous cell carcinoma (OSCC) is a common cancer worldwide, and the incidence has been rising steadily. Of great concern is the growing proportion of younger patients without a history of smoking or alcohol abuse among OSCC patients. Currently, the primary treatment of OSCC patients comprises surgery and (chemo) radiotherapy, either alone or in combination. Other clinically approved approaches, such as targeted- and immuno-therapies, remain inconsistently applied as a first-line treatment for OSCC patients. Unfortunately, despite the advancement in cancer management, these treatments offer limited efficacy and the 5-year survival rate among OSCC patients is around 50–60% [1, 2].
Angiogenesis is a key process in the tumorigenesis of solid cancers, promoting tumor growth, recurrence and metastasis. A large body of evidence suggested that targeting angiogenesis could provide a clinical benefit in the treatment of solid tumors [3]. Thus, the US Food and Drug Administration (FDA) approved the first angiogenesis inhibitor for cancer treatment—bevacizumab (Avastin®)—in February 2004. Bevacizumab, a recombinant monoclonal antibody targeting all isoforms of vascular endothelial growth factor (VEGF), has been approved initially for treating patients with metastatic colorectal cancer in combination with chemotherapy [4]. Since then, bevacizumab has initiated a new era in anticancer therapy, and anti-angiogenic drugs are now indicated for treating different malignancies including glioblastoma, breast, lung, ovarian, and cervical cancers. However, there are no FDA-approved anti-angiogenic drugs for head and neck squamous cell carcinoma (HNSCC) including OSCC, although these cancers arise in highly vascularized tissues [3, 5].
In spite of the promising results from some preclinical models, anti-angiogenic agents have revealed a considerable toxicity and limited clinical success in HNSCC patients [6]. This could be attributed, at least in part, to various tolerance mechanisms including an intrinsic or acquired drug resistance and the formation of tumor cell-derived mimetic vessels [3, 7]. In this Research Topic, Salem and Salo reviewed the vasculogenic (or vascular) mimicry (VM), a new paradigm of tumor cell-associated neovascularization that was introduced at the end of the previous millennium. VM describes the ability of certain aggressive tumors to initiate perfusable, matrix-rich, vessel-like networks in collagen-rich matrices in vitro and in vivo. This phenomenon has ignited a vibrant research interest and revealed promising prognostic and therapeutic implications. Further, it provides a possible explanation of the modest anti-angiogenic drug response in cancer patients. This review summarized the available knowledge regarding VM formation in HNSCC ranging from the characterization protocols to the prognostic value and limitations. Finally, the authors presented a potential novel mechanism of lymphatic metastasis in HNSCC—lymphatic mimicry (LM). Mirroring VM, this concept describes a process whereby tumor cells form mosaic vessel-like structures expressing tumor and lymphatic cell markers in OSCC tissues and in vitro. These LM structures influenced tumor cell invasion and metastasis and could provide avenues for developing anti-lymphangiogenic drugs in HNSCC [8].
In their research on medicinal natural compounds, Pang et al. showed that GT198, a protein inducing angiogenesis in OSCC, can be targeted by anticancer agents and herbs. Of interest, several clinically valid drugs inhibited the activity of GT198, including but not limited to mitoxantrone, doxorubicin and imatinib. A strong inhibition was further seen when applying certain anticancer herbs such as allspice, Gleditsia sinensis or honey locust. These findings could open an opportunity to identify potential antiangiogenic natural drugs with high efficacy and low toxicity for treating patients with oral cancer.
Although OSCC is the most common tumor type in the head and neck region, other less frequent, yet highly aggressive, tumors can also be encountered in the oral cavity. In this regard, Suzuki et al. studied an angiogenesis-associated pathway in salivary duct carcinoma (SDC), a cancer that can arise as a primary tumor (de novo) or from recurrent carcinoma ex-pleomorphic adenoma (Ca-ex-PA). Similar to the ductal breast carcinoma, SDC is characterized by an induced human epidermal growth factor receptor 2 (HER2) status. In the study included in this Research Topic, authors conducted immunostaining and dual color in situ hybridization of HER2 (Di Palma Classification) for patients with SDC, and analyzed the expression levels of 84 functional genes using PCR. Of note, significant differences in gene expression were found between Ca-ex-PA and de novo tumors. VEGF-A was significantly induced in the Ca-ex-PA, which can be a crucial factor in the malignant conversion to SDC through angiogenesis and the AKT/PI3K signaling pathway. Multiple machine learning methods confirmed that the prominent proangiogenic factor VEGF-A can be a candidate for differentiating Ca-ex-PA from de novo lesions.
Since oral cancer continues to constitute a substantial health and economic burden worldwide, we hope that this Research Topic will be informative to clinicians, researchers, and health care providers.
Author Contributions
All authors listed have made a substantial, direct, and intellectual contribution to the work and approved it for publication.
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.
Publisher's Note
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References
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6. Hyytiäinen A, Wahbi W, Väyrynen O, Saarilahti K, Karihtala P, Salo T, Al-Samadi A. Angiogenesis inhibitors for head and neck squamous cell carcinoma treatment: is there still hope? Front Oncol. (2021) 14:683570. doi: 10.3389/fonc.2021.683570
7. Ebos JM, Lee CR, Kerbel RS. Tumor and host-mediated pathways of resistance and disease progression in response to antiangiogenic therapy. Clin Cancer Res. (2009) 15:5020–5. doi: 10.1158/1078-0432.CCR-09-0095
Keywords: oral cancer (OC), angiogenesis, angiogenesis inhibitor, head and neck squamous cell carcinoma (HNSCC), vasculogenic mimicry (VM), salivary duct carcinoma (SDC), oral squamous cell carcinoma
Citation: Salem A, Hadler-Olsen E and Al-Samadi A (2021) Editorial: Angiogenesis and Angiogenesis Inhibitors in Oral Cancer. Front. Oral. Health 2:816963. doi: 10.3389/froh.2021.816963
Received: 17 November 2021; Accepted: 23 November 2021;
Published: 15 December 2021.
Edited and reviewed by: Ricardo D. Coletta, Campinas State University, Brazil
Copyright © 2021 Salem, Hadler-Olsen and Al-Samadi. 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: Abdelhakim Salem, abdelhakim.salem@helsinki.fi