WenJuan Wang
Guodong Li1
Qingjian He- 1Department of Cardiovascular Center, The First People’s Hospital of Huzhou City, Huzhou, China
- 2Department of Hypertension Center, Lanzhou University Second Hospital, Lanzhou, China
- 3Department of Breast and Thyroid Surgery, The First People’s Hospital of Huzhou City, Huzhou, China
With the advancement of tumour-targeted therapy technology, the survival of cancer patients has continued to increase, and cardiovascular events have gradually become an important cause of death in cancer patients. This phenomenon occurs due to adverse cardiovascular reactions caused by the cardiovascular toxicity of antitumour therapy. Moreover, the increase in the proportion of elderly patients with cancer and cardiovascular diseases is due to the extension of life expectancy. Hypertension is the most common cardiovascular side effect of small molecule tyrosine kinase inhibitors (TKIs). The increase in blood pressure induced by TKIs and subsequent cardiovascular complications and events affect the survival and quality of life of patients and partly offset the benefits of antitumour therapy. Many studies have confirmed that in the pathogenesis of hypertension, arterioles and capillary thinness are involved in its occurrence and development. Our previous findings showing that apatinib causes microcirculation rarefaction of the superior mesenteric artery and impaired microvascular growth may inspire new therapeutic strategies for treating hypertension. Thus, by restoring microvascular development and branching patterns, total peripheral resistance and blood pressure are reduced. Therefore, exploring the key molecular targets of TKIs that inhibit the expression of angiogenic factors and elucidating the specific molecular mechanism involved are key scientific avenues for effectively promoting endothelial cell angiogenesis and achieving accurate repair of microcirculation injury in hypertension patients.
1 Introduction
Hypertension has a high prevalence in China and accounts for a large proportion of cardiovascular diseases. Hypertension is also a major risk factor for cardiovascular-related diseases. In recent years, a number of studies have reported a relationship between tumours and hypertension. Tumours and hypertension have common risk factors and overlapping pathophysiological mechanisms (Milan et al., 2014; Bray et al., 2021; Dolmatova et al., 2023). Therefore, several experts have gradually formed the theory of onco-hypertension. Previous studies by our group have shown that hypertension and antihypertensive drug use are closely related to breast cancer. With increasing age, the incidence of hypertension in breast cancer patients increases, and the mechanism is related to inflammatory mediators and angiogenesis (Zhao et al., 2018; Wang et al., 2021). Another reason is that women’s estrogen levels decline as they age. Estrogen has a protective effect on blood vessels, so such patients are more likely to induce hypertension. And estrogen for breast cancer patients, with the increase of age, although estrogen in the body decreases, but some patients may be converted to androgen, leading to the increase in the incidence of breast cancer. In recent years, new antineoplastic drugs have prolonged the survival of cancer patients, but the increase in blood pressure caused by new antineoplastic drugs and the subsequent cardiovascular complications and events affect the survival and quality of life of patients, which partly offset the benefits of antineoplastic therapy. It is worth exploring this topic further.
2 Incidence of hypertension caused by TKIs
VEGF signalling pathway inhibitors include monoclonal antibodies against VEGF A factor, VEGF traps, monoclonal antibodies against VEGF receptors, and TKIs (Pucci et al., 2019; Le et al., 2021; Lawler, 2022). Studies have shown that the probability of hypertension caused by VEGF signalling pathway inhibitors during antitumour therapy is approximately 11%–45%, among which the incidence of hypertension above grade 3 (referring to CTCAE grade 3–4, that is, SBP≥160 and/or DBP ≥100 mmHg) or life-threatening hypertension, even requiring emergency treatment, ranges from 2 to 20% (Xu et al., 2021). According to the type and dose of TKIs, the incidence of hypertension can reach 20%–90%, and the incidence of severe hypertension can reach 6%–43% in patients using TKIs alone or in combination. The incidence of hypertension induced by TKIs is shown in Table 1.
TABLE 1. Incidence of hypertension caused by TKIs.
Apatinib mesylate is an antitumour drug that was independently developed in China and belongs to the class of TKIs. In the past, it was mainly used for the treatment of solid tumours, such as advanced gastric cancer or gastroesophageal junction adenocarcinoma (Li et al., 2016). An international multicentre phase III study (SHR-1210-III.-310 study) demonstrated that the approved PD-1 inhibitor camrelizumab in combination with apatinib had a significant survival benefit and a tolerable safety profile in the first-line treatment of advanced liver cancer, with a median overall survival (OS) of 22.1 months. It is the combination therapy with the longest OS benefit in the first-line treatment of advanced liver cancer (Qin et al., 2023). Therefore, the National Medical Products Administration (NMPA) proposed the combination of “Shuang’ai" for the first-line treatment of advanced hepatocellular carcinoma, which is the first approval in China to use a combination of PD-1 inhibitors and TKIs for the treatment of advanced hepatocellular carcinoma. The application of this treatment regimen has led to new drug options for patients with advanced liver cancer. The resulting cardiovascular side effects of nitrogen are also very noteworthy. Therefore, studying the cardiovascular toxicity and side effects caused by TKIs is highly important for guiding antitumour therapy in clinical cancer patients.
3 Causal relationship between microcirculation damage and hypertension
3.1 Microcirculation and related definitions of microcirculation damage
Microcirculation typically includes small resistance arteries (300–100 µm in diameter), precapillary arterioles (100–10 µm), capillaries (5–15 µm) and venules (10–100 µm) (le Noble et al., 2023). Various studies have shown that damage to microcirculatory tissue may involve multiple mechanisms. The main categories of such damage include impaired endothelial cell function, oxidative stress, decreased angiogenesis (most commonly in patients after the use of targeted drugs), increased endothelial permeability, enhanced leukocyte adhesion, immune cell activation, lymphatic dysfunction, impaired autoregulation, microvascular constriction, and microcirculation obstruction (Sorop et al., 2020; Sabe et al., 2022; De Ciuceis et al., 2023; Mengozzi et al., 2023).
3.2 Microcirculation and types of microcirculation damage
Studies have shown a relationship between hypertension and changes in the microvascular network in spontaneously hypertensive rats (SHRs), with reduced arteriolar density and increased postcapillary venule density (Martens and Gelband, 1998). It lead to increased postvascular resistance, which may further contribute to the development of hypertension. In addition, it has been shown that a sparse microvascular network structure increases total peripheral resistance, which eventually leads to increased blood pressure (le Noble et al., 2023). Many previous studies have confirmed the importance of arteriolar and capillary scarcity in the pathogenesis of hypertension (Levy et al., 2001; Levy et al., 2008). That is, the rarefaction of capillaries may contribute to the development of hypertension.
Microcirculation injury can occur through two main forms of microvascular rarefaction (Agabiti-Rosei, 2003; Ungvari et al., 2021). Functional rarefaction means that the total number of anatomically present vessels is not reduced but rather that perfusion of this part of the microvascular network is absent. However, as the vascular tone continues to increase, the lumen area increases, resulting in a decrease in the number of blood vessels perfused. Structural sparseness also occurs, which reduces the number of blood vessels that can be found during tissue dissection. This reduction in vascular mesh may be due to altered anatomical changes in the vascular segments or other impairments in the vascular network during the growth and development process during early tissue development. Several experts have also noted that functional rarefaction can progress to structural rarefaction in a rat model of SHR. However, there are also studies showing that patients with essential hypertension, recruitment of perfused capillaries is impaired, which can be explained by both functional and structural rarefaction (Serné et al., 2001). Therefore, whether the microcirculation dilution in hypertension is structurally sparse or functional, or even both, will be our further research plan. This part of the study is crucial for them to identify the specific microcirculation sparse so that we can improve and treat it according to the cause, especially in patients with hypertension caused by targeted drugs.
3.3 Mechanisms of microcirculation damage leading to hypertension
Microvascular injury plays an indispensable role in the occurrence and development of hypertension, and some studies have shown that it plays an important role in the progression of hypertension, hypertension-mediated organ damage and related cardiovascular events (Jonk et al., 2007; Karaca et al., 2014; Rizzoni et al., 2023). However, the causal relationship between thinning of microvessels and hypertension is difficult to explain, and some experts speculate that diffuse generalized thinness of microvessels may be one of the main causes of hypertension (Marinescu et al., 2015; Horton and Barrett, 2021). In study, after 5 weeks of treatment with telatinib, the capillary density decreased from 20.8 at baseline to 16.7 (Steeghs et al., 2008). Mourad et al. reported a significant reduction in kinetic and structural capillary density in a group of patients with metastatic colon cancer treated with bevacizumab for 6 months (Mourad et al., 2008). However, this rarefaction is most likely functional because blood pressure increases rapidly after the start of treatment and returns to normal immediately after the discontinuation of VEGF inhibitors (van Dorst et al., 2021). Therefore, further studies to determine whether microvascular thinning is the cause or effect of the actions of VEGF inhibitors on hypertension are highly clinically important.
Animal experiments revealed that a rise in blood pressure leads to an increase in the production of reactive oxygen species in mice. Therefore, researchers have speculated that elevated blood pressure may be responsible for microvascular function and structural alterations, further contributing to the manifestation of vascular thinning (Ungvari et al., 2004; Jacobson et al., 2007). However, there is considerable evidence that microvascular changes may also be a cause rather than a consequence of hypertension. In animal models of hypertension, increased reactive oxygen species production and sparse arterioles occur even in the vasculature not exposed to hypertension (Boegehold et al., 1991). Our previous results showed that blood pressure was significantly increased in an apatinib-treated mouse model of gastric cancer, and sparsity of arteriolar vessels was detected in the mesenteric arteries of experimental model mice. Therefore, we speculate that the microcirculation damage caused by apatinib during antitumour treatment may be one of the main causes of hypertension. However, this study did not further confirm whether functional or structural vascular alterations are the cause, and it is very important to clarify this classification for the treatment of hypertension induced by TKIs. Because we did not further lower the blood pressure after the elevation of blood pressure, we investigated whether the vascular density of the superior mesenteric artery in the mice was further restored.
In addition, microvascular rarefaction is observed in the early stages of hypertension development, and microvascular rarefaction can be detected in individuals with a family history of hypertension, even if their blood pressure is normal. Similarly, in animal experiments, microvascular abnormalities occur early in the development of hypertension in SHRs (Antonios et al., 2003). In addition, the latest results from our research indicated that the administration of the ROCK inhibitor Y27632 can prevent microvascular rarefaction caused by apatinib and improve blood pressure (Wang et al., 2022a). Thus, microvascular growth disorders may have given rise to a new paradigm of hypertension treatment aimed at restoring microvascular development and branching, thereby further reducing peripheral resistance and improving the structural reduction of arterial blood pressure.
4 Relationship between microcirculation-induced hypertension and heart failure
Hypertension is an important risk factor for heart failure (Garg et al., 2021). Long-term uncontrolled hypertension can exert excessive pressure on the heart and gradually impair heart function, leading to cardiac hypertrophy and decreased myocardial contractility. Over time, this overload can impede the ability of the heart to pump blood effectively, triggering heart failure (Slivnick and Lampert, 2019; Jackson et al., 2021; Redfield and Borlaug, 2023). The most common type of heart failure is heart failure with preserved ejection fraction (HFpEF). There are multiple mechanisms involved in the development of hypertension from HFpEF, and these mechanisms can be divided into several categories. The most common is microcirculatory dysfunction, which mainly includes an increase in inflammatory factors, the occurrence of oxidative stress, impaired endothelial function, and the occurrence of vascular endothelial fibrosis (Gryglewska et al., 2011; Paulus and Tschöpe, 2013; Stupin et al., 2021; Marra et al., 2022).
Firstly, left atrial pressure increases in hypertensive patients, with a consequent increase in left ventricular end-diastolic pressure, and left atrial remodeling occurs. This process is an indication of left ventricular diastolic dysfunction. Left atrial enlargement and dysfunction, including reduced left atrial systolic reserve, can eventually lead to the development of HFpEF (Nagai et al., 2023; Li et al., 2024). Secondly, in patients with chronic systemic inflammation such as hyperemia, systemic secreted inflammatory cytokines can cause the accumulation and inflammatory response of epicardial adipose tissue, which can promote the migration and transformation of mesenchymal stem cells and local secretion of inflammatory cytokines, leading to deep myocardial cell inflammation, increased myocardial stiffness, deep myocardial fibrosis, and finally HFpEF (Obokata et al., 2017; Gevaert et al., 2022; Gao et al., 2023; Rossi et al., 2023). In addition, microcirculation disorders also play an important role in the occurrence and development of HFpEF (Camici et al., 2020). Systemic inflammation can lead to microvascular inflammation and endothelial activation, resulting in significant structural and functional changes in cardiomyocytes and extracellular matrix, including the decrease of NO and vasodilator peptide levels, which leads to the enhancement of vasoconstriction, left ventricular stiffness and myocardial collagen-ization, and ultimately the formation of HFpEF (Vancheri et al., 2020; Agrawal et al., 2023). Overall, in most patients with hypertension, left ventricular diastolic dysfunction is the first apparent manifestation of heart failure. Our previous study (Wang et al., 2022a) showed that apatinib increased blood pressure in gastric cancer model mice, which further led to left ventricular hypertrophy and fibrosis. Therefore, exploring the mechanism through which apatinib-induced hypertension leads to HFpEF in gastric cancer mice is highly important, as is exploring drugs that can delay the progression of HFpEF.
Abnormal structure and function of miniscule arteries and capillaries results in hypoperfusion of blood flow (Mourad and Levy, 2011; Struijker-Boudier and Heijnen, 2011; Wu et al., 2023). Studies have shown that sparse microcirculation may be one of the main causes of hypertension (Ciuffetti et al., 2003). Chronic high blood pressure damages the heart and blood vessels. Pathological changes in miniscule arteries and capillaries, such as intimal thickening, fibrosis, and luminal narrowing, further inhibit blood flow perfusion (Triantafyllou et al., 2015). This microcirculatory pathology affects normal oxygen availability and nutrient delivery to the heart and other tissues (De Backer et al., 2014; Cusack et al., 2022). Ischaemia and hypoxia lead to cardiac cell damage and death, which eventually leads to weakened cardiac systolic function and the occurrence of heart failure (Premont et al., 2020). Therefore, microcirculatory impairment plays a key role in hypertension and cardiac dysfunction. Therefore, protecting microcirculation function is highly important for the prevention and treatment of hypertensive heart failure.
5 Mechanisms related to hypertension caused by TKIs
5.1 Relationship between VEGF signaling pathway and TKI-induced hypertension
The most common pathways are the vascular endothelial growth factor (VEGF), platelet-derived growth factor (PDGF), angiopoietin-1, and Notch signalling pathways (Viallard and Larrivée, 2017; Vimalraj, 2022; Huang et al., 2023) and so on. VEGF is one of the most important proangiogenic mediators. Recently, studies have shown that VEGF is the core factor affecting endothelial cell angiogenesis and is closely related to hypertensive microcirculation damage (Chade and Kelsen, 2010). However, the foundation of TKI antitumour therapy is the inhibition of vascular endothelial growth factor, which brings certain challenges to antitumour therapy. The latest research from our team revealed that in a mouse model of gastric cancer, the mechanism of apatinib-induced hypertension in mice may be related to the sparse vascular density of the superior mesenteric artery (Wang et al., 2022a).
VEGF signaling pathway inhibitors include monoclonal antibodies against VEGFA, vascular endothelial growth factor inhibitors (VEGF trap), monoclonal antibodies against VEGF receptors, and TKIs (Saif, 2013; Shughoury et al., 2023). TKIs are effective signaling cascade inhibitors that inhibit tumor blood vessel growth by inhibiting vascular endothelial growth factor receptor (VEGFR) (Vano et al., 2022). VEGFR-TKIs have become the main treatment for many solid malignant tumors. However, TKIs can induce vascular endothelial damage, hypertension and myocardial injury by targeting VEGFR, platelet-derived growth factor receptor (PDGFR) and stem cell factor receptor (SCFR) (van Cruijsen et al., 2009; Lennartsson and Rönnstrand, 2012). It can also damage mitochondria and affect myocardial energy metabolism through the “off-target effect", eventually leading to cardiovascular complications (Tullemans et al., 2018; Rodríguez-Agustín et al., 2023). Therefore, the incidence of cardiovascular toxicity related to VEGFR-TKIs is high, which can cause the occurrence and development of cardiovascular complications such as hypertension, left ventricular systolic dysfunction/heart failure, and atherosclerosis.
Anti-angiogenesis targeting drugs mainly act on VEGF and VEGFR. VEGFR-1, VEGFR-2 and VEGFR-3 are the major VEGF receptors (Sallinen et al., 2009; Bernatz et al., 2021). VEGF inhibitors can increase the risk of heart failure, coronary heart disease, hypertension and thromboembolic diseases through endothelial injury, vasoconstriction and remodeling, inflammatory response and platelet activation.
5.2 Relationship between RhoA/ROCK signaling pathway and TKIs-induced hypertension
In addition, the latest study from our team revealed that apatinib has a considerable therapeutic effect on a mouse model of gastric cancer (Wang et al., 2022a). However, apatinib can also lead to an increase in blood pressure, accompanied by activation of the RhoA/ROCK signalling pathway. And the ratio between vessel thickness and lumen diameter was significantly increased in the apatinib group. We also observed that apatinib in combination with the ROCK inhibitor Y27632 did not affect the antitumour therapeutic effect of apatinib. Finally, our combined administration of ROCK inhibitors significantly reduced the increase in blood pressure in an apatinib-induced gastric cancer mouse model (Wang et al., 2022a). Therefore, Y27632 has wide application prospects for the treatment of tumour-induced hypertension.
Further studies at the cellular level have shown that knocking down the key gene LRAG in the RhoA/ROCK signalling pathway can improve the abnormal proliferation and impaired cell function of vascular smooth muscle cells caused by apatinib (Wang et al., 2022b). This is mainly because apatinib can increase blood pressure by activating the RhoA/ROCK signaling pathway. Therefore, exploring the key molecular targets of TKIs that inhibit the expression of angiogenic factors and elucidating the specific molecular mechanism involved are key for effectively promoting endothelial cell angiogenesis and achieving accurate repair of microcirculation injury in hypertension patients.
5.3 Relationship between notch signaling pathway and TKIs-induced hypertension
Notch and DLL4 are specifically expressed on vascular endothelial cells (EC). JAG has been shown to promote cell survival and proliferation, interacting with NOTCH and hematopoietic stem and progenitor cells (HSPCs) (Kangsamaksin et al., 2015). In addition, high expression of JAG promotes cancer development. We hypothesized that inhibition of Notch signaling activation would not only inhibit tumor development, but also help angiogenesis. Therefore, exploring the mechanism of angiogenesis dysfunction induced during antitumour therapy is highly clinically important.
Notch signalling pathway, as a classical signaling pathway, is closely related to cardiovascular and tumor microcirculation. Combined with our previous results, Notch signaling pathway may also be involved in TKI-induced blood pressure elevation. The regulation of the Notch signalling pathway is closely related to the proliferation, migration and tube formation of vascular endothelial cells during tumour angiogenesis. Further research on the relationship between the Notch signalling pathway and tumour-related cardiovascular disease is expected to lead to new therapeutic strategies and targets for the prevention and treatment of tumours.
5.4 Other mechanisms associated with TKIs-induced hypertension
At present, there are many studies on hypertension caused by TKIs, and the relevant mechanisms involved may be related to the following aspects: 1) decreased bioavailability of nitric oxide (Robinson et al., 2010); 2) enhanced oxidative stress (Neves et al., 2018); 3) increased secretion of endothelin-1 (Mirabito Colafella et al., 2020); 4) decreased bioavailability of prostacyclin (Wheeler-Jones et al., 1997); 5) increased bioavailability of endothelial microparticles (Neves et al., 2019); 6) sparse microvessels (Steeghs et al., 2008); 7) vascular sclerosis (Catino et al., 2018); 8) activation of renin angiotensin (Li et al., 2022); and 9) salt-sensitive hypertension (Tsai et al., 2017).
6 Role of the notch signalling pathway in the cardiovascular system
The Notch signalling pathway is a common signalling pathway that plays a certain role in cell development. The Notch protein is a transmembrane receptor that is located on the cell surface and mediates important cellular functions (Kwak et al., 2022; Takahashi et al., 2023). The interaction between the Notch protein and its ligand initiates a signalling cascade associated with cell fate that plays a key role in differentiation, proliferation, and apoptosis in many tissue types (Zhao et al., 2019; Li et al., 2020). The Notch protein, as well as its ligand, contains extracellular EGF-like repeats that interact with the DSL domain of the ligand. Activation of the Notch signalling pathway is accompanied by proteolysis, which releases the intracellular domain of Notch (NICD) (Sprinzak and Blacklow, 2021; Fang et al., 2022). The NICD is a fragment containing a RAM23 domain (RAM) that can enhance interactions with the Notch and CSL proteins, thereby facilitating the transmission of Notch to the nuclear localization signal (NLS) (Lubman et al., 2007; Johnson and Barrick, 2012). The NICD fragment can further mediate interactions with other proteins in the Notch signalling pathway (Figure 1).
FIGURE 1. Notch proteins are cell surface transmembrane-spanning receptors that mediate critically important cellular functions through direct cell‒cell contact. EGF: epidermal growth factor, NICD: intracellular domain of Notch, NLS: nuclear localization signal, CSL: CBF1/Su(H)/Lag-1.
The VEGF signalling pathway interacts with the Notch signalling pathway, coordinates the differentiation of arteries and veins, and is also involved in changes in vascular budding and vascular branching (Laham et al., 2003; Li et al., 2017; Souilhol et al., 2022; Li et al., 2023a). In addition, the VEGF signalling pathway can regulate key processes such as lumen remodelling of blood vessels.
Microvascular rarefaction leading to hypertension involves multiple signalling pathways, such as vascular endothelial development, angiogenesis, inflammation, oxidative stress, and endogenous short peptides (Feihl et al., 2008; Bruno et al., 2018; Do et al., 2023; Zdravkovic et al., 2023). Vascular endothelial cells play a key role in maintaining normal vascular biological function and regulating vascular tone. The abnormal regulation of vascular endothelial growth factor and platelet-derived growth factor during angiogenesis may also be involved in the occurrence of microvascular rarefaction (Cohen et al., 2023). Studies have shown that the Notch signalling pathway plays an important role in angiogenesis (Maynard et al., 2003).
The Notch signalling pathway plays a key role in the regulation of angiogenesis, especially in balancing the proangiogenic effects of the VEGF signalling pathway. The Notch signalling pathway antagonizes angiogenesis via VEGF signalling. It also stimulates quiescent endothelial cells and promotes apical cell formation. Thus, this pathway mediates the formation of vascular buds and the further growth of new vascular buds (Marinescu et al., 2015). Under conditions of stress, the cascade between Dll4-mediated Notch signalling and VEGFA-VEGFR2 signalling induces endothelial cells adjacent to the dominant TCS to maintain high levels of Notch signalling, thereby inhibiting their differentiation into TCShh cells. Furthermore, it can inhibit angiogenesis (Gerhardt et al., 2003; Jakobsson et al., 2010; Herbert and Stainier, 2011). Angiogenesis inhibition is thought to be controlled by Notch 1-mediated downregulation of Flt 4 and upregulation of soluble Flt 1 (sVEGFR-1/sFlt 1) (Chappell et al., 2009; Trindade et al., 2012). In particular, upregulation of sFlt1 reduces local VEGF bioavailability and inhibits angiogenesis. The Notch ligand Jag 1 is expressed mainly in stem cells and is thought to specifically block Dll 4-Notch 1 signalling in apical cells (Benedito et al., 2009). In the cardiovascular system, excessive activation of the Notch signalling pathway can lead to vascular endothelial cell proliferation and congestion and an increase in vessel wall thickness, which leads to vascular stenosis and hypertension (Niessen and Karsan, 2007; MacGrogan et al., 2018; Gomez et al., 2021).
The Notch signalling pathway is also involved in the occurrence and development of heart failure. Activation of Notch signalling can lead to cardiomyocyte proliferation and hypertrophy and can also affect angiogenesis and repair processes in the cardiovascular system (Fortini et al., 2014; Matsushita et al., 2023). These changes may adversely affect myocardial function and lead to the development of heart failure. Notch1 is a transmembrane receptor found in a variety of cells, including smooth muscle cells and endothelial cells in the cardiovascular system. During heart wall formation, Notch signalling regulates the ratio of cardiomyocytes to noncardiomyocytes by inhibiting myogenesis, thereby further promoting atrioventricular canal remodelling and maturation and heart valve formation (Niessen et al., 2011; Peng et al., 2023). Activation of the Notch1 signalling pathway is achieved mainly through the binding of the Notch1 receptor to its ligand. When the Notch1 receptor binds to its ligand, secondary cleavage occurs, and the active region of the Notch1 receptor is released. Then the receptor enters the nucleus and interacts with transcription factors to promote gene transcription and expression (Wang S. et al., 2022). Studies have also shown that activation of the Notch1 signalling pathway is closely related to cardiac function and can affect the proliferation and differentiation of cardiomyocytes, thus affecting the development and function of the heart (Pahlavani, 2022). In addition, activation of the Notch1 signalling pathway can also regulate the expression of the actin gene in cardiac cells, affecting cardiac contractility and cardiac contraction rhythm (Hrstka et al., 2017). Therefore, the Notch signalling pathway plays an integral and critical role in maintaining and regulating blood pressure and cardiac function.
7 Role of the notch1 signalling pathway in tumour systems
The Notch signalling pathway is involved in cell-to-cell interactions and communication and plays an important role in embryonic development and the maintenance of tissue homeostasis in adult organisms. Moreover, aberrant Notch signalling pathway activity has also been found to be closely related to the occurrence and development of a variety of tumour types.
In terms of tumours, studies have shown that abnormal activation of the Notch1 signalling pathway is related to the occurrence and development of a variety of diseases, such as tumour proliferation and metastasis and abnormal responses of the immune system (Yang et al., 2018; Peng et al., 2023). Therefore, we hypothesized that inhibition of the Notch1 signalling pathway may ameliorate the adverse effects on blood pressure and cardiac function. Therefore, what is the underlying mechanism involved in reducing blood pressure and cardiac dysfunction? This will be another important dimension that needs to be studied.
In hepatocellular carcinoma (HCC), Notch signalling is activated by different ligands and plays a polymorphic role depending on the cell type, affecting tumour growth, invasive ability, and stem cell-like properties (Giovannini et al., 2021). Thus, interfering with Notch signalling may be a promising therapeutic approach. In tumour therapy, the downregulation of Notch1 can achieve synergistic effects and reduce chemoresistance when targeted drugs are used alone or in combination with chemotherapy. In addition, Notch mutations have been proposed to be predictive biomarkers for immune checkpoint blockade therapy in many cancers (Zhou et al., 2022; Li et al., 2023b).
8 Possible treatment of hypertension and myocardial damage caused by the notch signalling pathway
Recently, it has been observed that Epac1 can negatively regulate the Notch signalling pathway. Epac1 knockdown in endothelial cell lines resulted in a significant increase in the intracellular Notch1 protein level, and Epac1 knockdown increased the protein levels of NICD and DLL4, thereby further inhibiting angiogenesis. Therefore, overexpression of Epac1 may be an effective way to alleviate microvascular rarefaction (Fritz et al., 2015; Lan et al., 2020; Slika et al., 2023). Interestingly, studies have shown that Epac1 knockdown can inhibit pathological angiogenesis but has no significant effect on physiological angiogenesis, which is worthy of attention and discussion (Lan et al., 2020). Previous studies have shown that Epac1 is a β-secretase enzyme that inhibits the activation of the Notch signalling pathway (Fujita et al., 2017; Tan et al., 2022). In addition, Epac1 has been shown to enhance the VEGF signalling pathway and promote pathological angiogenesis (Namkoong et al., 2009; Ramos et al., 2018). Therefore, we speculate that the occurrence of hypertension caused by TKIs may lead to microcirculation disorders and microvascular thinning, and overexpressing the Epac1 gene may be a very meaningful way to improve or treat microvascular thinning caused by TKIs. NOTCH mutations can be used as predictive markers for treatment with immune checkpoint blockade in some tumors. In summary, it is necessary to comprehensively evaluate the NOTCH pathway from a new perspective, so as to apply it in the subsequent clinical diagnosis and treatment.
9 Mitochondrial dysfunction may also be involved in the regulation of notch signalling
In addition, Epac1 can play a role in cell-to-cell molecular conduction by increasing its interaction with macromolecular complexes, including voltage-dependent anion channel 1 (VDAC1), chaperone glucose-regulated protein 75 (GRP75), and inositol triphosphate receptor 1 (IP3R1). The interaction between Epac1 and macromolecular complexes can further promote the exchange of Ca2+ between the endoplasmic reticulum and mitochondria, which can eventually lead to mitochondrial Ca2+ overload and the opening of mitochondrial permeability transition pores (Fazal et al., 2017). Therefore, Epac1 is expected to be a new target for the treatment of ischaemic myocardial injury.
Mitochondria are important organelles for cellular energy production, and dysfunction of these organelles plays a key role in the emergence and progression of cardiovascular diseases (Poznyak et al., 2021; Wu et al., 2022). Normally, mitochondrial proteostasis is monitored by an extensive system: the mitochondrial unfolded protein response (UPRmt) is activated when mitochondria are stimulated by misfolded protein stress. The latter promotes the upregulation of ClpP, HSP6, HSP-60, ATFS-1 and other markers through a series of signalling cascades to alleviate mitochondrial stress (Merkwirth et al., 2016; Kumar et al., 2022; Xin et al., 2022; Guo et al., 2023). Under conditions of stress, cells can protect mitochondria by activating the UPRmt. It has been shown that the inhibition of Epac1 prevents ferroptosis-induced cell death and disruption of mitochondrial integrity, whereas the inhibition of Epac2 has a limited effect (Laudette et al., 2021; Musheshe et al., 2022). However, the potential effects of Epac on mitochondrial function are still unclear, and additional experiments are needed for further elucidation.
Several studies have shown that UPRmt activation is accompanied by the upregulation of the mitophagy markers PINK1, PARK2, BNIP3, P62, and LC3 and the mitochondrial oxidative phosphorylation (OXPHOS) markers Cox5a, Cox2, Nd1, and Sdhc. These results indicate that the UPRmt, mitophagy and OXPHOS play synergistic roles in maintaining mitochondrial protein balance and mitochondrial function (Kang et al., 2017; Martinez et al., 2017; Sorrentino et al., 2017; Poole and Macleod, 2021). The latest article published in NATURE refers to a series of mitochondrial stress responses that cause abnormal changes in the UPRmt, mitophagy, and OXPHOS under specific pathological or stimulus conditions, such as the mitochondrial stress response (MSR) (Ruan et al., 2017; Sorrentino et al., 2017; Jakobsen et al., 2019). The MSR is a key mechanism regulating mitochondrial protein balance and the mitochondrial stress response. EPAC1 can activate the UPRmt and protect mitochondrial function. Additionally, it is a key molecule that regulates the UPRmt and mitophagy (Gariani et al., 2016; Jayarajan et al., 2019; Aslam and Ladilov, 2021).
10 Summary
TKIs can induce vascular endothelial damage, hypertension and myocardial injury by acting on the targets VEGFR, platelet-derived growth factor receptor (PDGFR) and stem cell factor receptor (SCFR). It can also damage mitochondria and affect myocardial energy metabolism through “off-target effects", eventually leading to cardiovascular complications. Therefore, the goal of antitumour therapy is to maximize the antitumour effect while reducing treatment-related cardiovascular events. Therefore, studying the mechanism of hypertension during the treatment of cancer patients with TKIs and finding compounds or key factors that can reduce blood pressure without affecting antitumour efficacy are highly valuable. We hypothesize that inhibition of Notch signalling could ameliorate TKI-induced microvascular rarefaction, thereby further ameliorating the increase in blood pressure or the resulting cardiac dysfunction caused by microvascular rarefaction. Overexpression of Epac 1, a key gene in the Notch1 signalling pathway, can improve the pathological vascular inhibition induced by TKIs. The mechanism by which apatinib, a representative TKI, induces microcirculation damage, hypertension and heart failure through the Notch1 signalling pathway will also be explored at the cellular and animal levels to provide clinical guidance for patients with hypertension induced by cancer treated with TKIs.
In summary, side effects such as cardiovascular toxicity caused by antitumour therapy with TKIs have become one of the main factors limiting antitumour therapy with TKIs. For the treatment of such hypertension, the effect of traditional antihypertensive drugs is not ideal, and traditional antihypertensive drugs are also closely related to the occurrence and development of some tumours. Exploring the underlying mechanism of cardiovascular complications caused by antitumour treatment with TKIs is crucial for ensuring the smooth clinical application of TKIs, and identifying this mechanism is also an urgent need. New directions for improving the treatment of hypertension induced by these drugs should be explored. The ultimate goal of our team will be to improve the clinical outcome as soon as possible and to provide greater benefits for cancer patients.
Author contributions
WW: Methodology, Resources, Writing–original draft, Writing–review and editing. GL: Investigation, Writing–review and editing. JM: Writing–review and editing. XF: Formal Analysis, Writing–review and editing. JL: Conceptualization, Writing–review and editing. QS: Supervision, Writing–review and editing. JY: Data curation, Writing–review and editing. QH: Conceptualization, Investigation, Supervision, Validation, Writing–review and editing.
Funding
The author(s) declare financial support was received for the research, authorship, and/or publication of this article. Funded by the Medical and Health Science and Technology Program of Zhejiang Province (2023KY1181).
Acknowledgments
We thank each editor and reviewer of this article, which has undergone a very careful and thorough review that greatly improved the original paper. We also thank all the participants at the First People’s Hospital of Huzhou and the Second Hospital of Lanzhou University.
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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Keywords: hypertension, microcirculation, rarefaction, TKIs, apatinib
Citation: Wang W, Li G, Ma J, Fan X, Lu J, Sun Q, Yao J and He Q (2024) Microvascular rarefaction caused by the NOTCH signaling pathway is a key cause of TKI-apatinib-induced hypertension and cardiac damage. Front. Pharmacol. 15:1346905. doi: 10.3389/fphar.2024.1346905
Received: 30 November 2023; Accepted: 30 January 2024;
Published: 09 February 2024.
Edited by:
Ismail Laher, University of British Columbia, CanadaReviewed by:
Qing Rex Lyu, Chongqing General Hospital, ChinaChristian Aalkjaer, Aarhus University, Denmark
Copyright © 2024 Wang, Li, Ma, Fan, Lu, Sun, Yao and He. 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: Qingjian He, 18742590857@163.com