Hsu Jui-Ling, Leu Wohn-Jenn, Hsu Lih-Ching, Hsieh Chia-Hsun, Guh Jih-Hwa
Department of Nursing, Division of Basic Medical Sciences, Chang-Gung University of Science and Technology, Taoyuan 333, Taiwan, R.O.C.
School of Pharmacy, College of Medicine, National Taiwan University, Taipei 100, Taiwan, R.O.C.
Oncol Lett. 2024 Feb 22;27(4):170. doi: 10.3892/ol.2024.14303. eCollection 2024 Apr.
Lung cancer is the leading cause of cancer-related death worldwide, and ~85% of lung cancers are non-small cell lung cancer (NSCLC), which has a low 5-year overall survival rate and high mortality. Several therapeutic strategies have been developed, such as targeted therapy, immuno-oncotherapy and combination therapy. However, the low survival rate indicates the urgent need for new NSCLC treatments. Vasculogenic mimicry (VM) is an endothelial cell-free tumor blood supply system of aggressive and metastatic tumor cells present during tumor neovascularization. VM is clinically responsible for tumor metastasis and resistance, and is correlated with poor prognosis in NSCLC, making it a potential therapeutic target. In the present study, A549 cells formed glycoprotein-rich lined tubular structures, and transcript levels of VM-related genes were markedly upregulated in VM-forming cells. Based on a drug repurposing strategy, it was demonstrated that doxazosin (an antihypertensive drug) displayed inhibitory activity on VM formation at non-cytotoxic concentrations. Doxazosin significantly reduced the levels of vascular endothelial growth factor A (VEGF-A) and matrix metalloproteinase-2 (MMP-2) in the cell media during VM formation. Further experiments revealed that the protein expression levels of VEGF-A and vascular endothelial-cadherin (VE-cadherin), which contribute to tumor aggressiveness and VM formation, were downregulated following doxazosin treatment. Moreover, the downstream signaling Ephrin type-A receptor 2 (EphA2)/AKT/mTOR/MMP/Laminin-5γ2 network was inhibited in response to doxazosin treatment. In conclusion, the present study demonstrated that doxazosin displayed anti-VM activity in an NSCLC cell model through the downregulation of VEGF-A and VE-cadherin levels, and the suppression of signaling pathways related to the receptor tyrosine kinase, EphA2, protein kinases, AKT and mTOR, and proteases, MMP-2 and MMP-9. These results support the add-on anti-VM effect of doxazosin as a potential agent against NSCLC.
肺癌是全球癌症相关死亡的主要原因,约85%的肺癌为非小细胞肺癌(NSCLC),其5年总生存率低且死亡率高。已经开发了几种治疗策略,如靶向治疗、免疫肿瘤治疗和联合治疗。然而,低生存率表明迫切需要新的NSCLC治疗方法。血管生成拟态(VM)是肿瘤新血管形成过程中存在的侵袭性和转移性肿瘤细胞的无内皮细胞肿瘤血液供应系统。VM在临床上与肿瘤转移和耐药有关,并且与NSCLC的不良预后相关,使其成为一个潜在的治疗靶点。在本研究中,A549细胞形成了富含糖蛋白的内衬管状结构,并且VM相关基因的转录水平在形成VM的细胞中显著上调。基于药物重新利用策略,证明多沙唑嗪(一种抗高血压药物)在非细胞毒性浓度下对VM形成具有抑制活性。多沙唑嗪在VM形成过程中显著降低了细胞培养基中血管内皮生长因子A(VEGF-A)和基质金属蛋白酶-2(MMP-2)的水平。进一步的实验表明,多沙唑嗪处理后,有助于肿瘤侵袭性和VM形成的VEGF-A和血管内皮钙黏蛋白(VE-钙黏蛋白)的蛋白表达水平下调。此外,响应多沙唑嗪处理,下游信号Ephrin A型受体2(EphA2)/AKT/mTOR/MMP/层粘连蛋白-5γ2网络受到抑制。总之,本研究表明多沙唑嗪通过下调VEGF-A和VE-钙黏蛋白水平以及抑制与受体酪氨酸激酶EphA2、蛋白激酶AKT和mTOR以及蛋白酶MMP-2和MMP-9相关的信号通路,在NSCLC细胞模型中显示出抗VM活性。这些结果支持多沙唑嗪作为一种潜在的抗NSCLC药物的附加抗VM作用。