Apigenin suppresses tumor angiogenesis and growth via inhibiting HIF-1? expression in non-small cell lung carcinoma
文献类型： 外文期刊
作者： Fu, Jijun 1 ; Zeng, Wenjuan 2 ; Chen, Minshan 1 ; Huang, Lijuan 1 ; Li, Songpei 1 ; Li, Zhan 1 ; Pan, Qianrong 1 ; Lv, Sha 1 ; Yang, Xiangyu 1 ; Wang, Ying 1 ; Yi, Mengmeng 3 ; Zhang, Jianye 1 ; Lei, Xueping 1 ;
作者机构： 1.Guangzhou Med Univ, Guangzhou Med Univ, Affiliated Hosp 5, Sch Pharmaceut Sci,Guangzhou Municipal & Guangdong, Guangzhou 511436, Peoples R China
2.Jinan Univ, Affiliated Hosp 1, Dept Obstet & Gynecol, 613, Huangpu Rd, Guangzhou, Peoples R China
3.Chinese Acad Fishery Sci, Pearl River Fisheries Res Inst, uangzhou, Peoples R China
关键词： Non-small cell lung carcinoma; Angiogenesis inhibitor; Apigenin; HIF-1?; Lung squamous carcinoma
期刊名称：CHEMICO-BIOLOGICAL INTERACTIONS （ 影响因子：5.168； 五年影响因子：4.924 ）
ISSN： 0009-2797
年卷期： 2022 年 361 卷
页码：
收录情况： SCI
摘要： Tumor angiogenesis inhibitors such as Bevacizumab, Ramucirumab and Endostar have been applied to the therapy of non-small cell lung carcinoma (NSCLC) patients, especially for lung adenocarcinoma (LUAD). However, several safe concerns such as neutropenia, febrile neutropenia and hypertension pulmonary hemorrhage limit their further development. And they often showed poor efficacy and serious side effect for lung squamous cell carcinoma (LUSC) patient. Thus, identification of effective and safe tumor angiogenesis inhibitor for NSCLC therapy is warranted. Apigenin is a bioflavonoid with potential anti-tumor effect and perfect safety, but its effect on tumor angiogenesis and underlying mechanism are still unclear. Herein, we found that apigenin not merely suppressed endothelial cells related motilities but also reduced pericyte coverage. Further research showed that apigenin had strong suppressive activity against HIF-1 alpha expression and its downstream VEGF-A/VEGFR2 and PDGF-BB/PDGF beta R signaling pathway. Apigenin also reduced microvessel density and pericyte coverage on the xengraft model of NCI-H1299 cells, leading to suppression of tumor growth. Moreover, apigenein showed perfect anti-angiogenic effect in xengraft model of LUSC cell NCI-H1703 cells, indicating it may be developed into a potential angiogenesis inhibitor for LUSC patient. Collectively, our study provides new insights into the antitumor mechanism of apigenin and suggests that apigenin is a safe and effective angiogenesis inhibitor for NSCLC therapy.
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