Zhang Pan, Lai Xing, Zhu Mao-Hua, Long Mei, Liu Xue-Liang, Wang Zi-Xiang, Zhang Yifan, Guo Run-Jie, Dong Jing, Lu Qin, Sun Peng, Fang Chao, Zhao Mei
Department of Pharmacy, Shanghai University of Medicine and Health Sciences, Shanghai, China.
Graduate School, Shanghai University of Traditional Chinese Medicine, Shanghai, China.
Front Pharmacol. 2021 Oct 29;12:713200. doi: 10.3389/fphar.2021.713200. eCollection 2021.
Saikosaponin A (SSA), a main triterpenoid saponin component from , has been revealed to have a variety of pharmacological activities. However, whether SSA can inhibit angiogenesis, a key step in solid tumor progression, remains unknown. In this study, we demonstrated that SSA could powerfully suppress the proliferation, migration, and tube formation of human umbilical vein endothelial cells. SSA also significantly inhibited angiogenesis in the models of the chick embryo chorioallantoic membrane and Matrigel plugs. Moreover, SSA was found to inhibit tumor growth in both orthotopic 4T1 breast cancer and subcutaneous HCT-15 colorectal tumor by the inhibition of tumor angiogenesis. Western blot assay indicated the antiangiogenic mechanism of SSA in the suppression of the protein phosphorylation of VEGFR2 and the downstream protein kinase including PLCγ1, FAK, Src, and Akt. In summary, SSA can suppress angiogenesis and tumor growth by blocking the VEGFR2-mediated signaling pathway.
柴胡皂苷A(SSA)是[来源植物名称未给出]的一种主要三萜皂苷成分,已被发现具有多种药理活性。然而,SSA是否能抑制实体瘤进展中的关键步骤——血管生成,仍不清楚。在本研究中,我们证明SSA能有力地抑制人脐静脉内皮细胞的增殖、迁移和管腔形成。SSA在鸡胚绒毛尿囊膜和基质胶栓塞模型中也显著抑制血管生成。此外,通过抑制肿瘤血管生成,发现SSA在原位4T1乳腺癌和皮下HCT - 15结直肠癌模型中均能抑制肿瘤生长。蛋白质印迹分析表明,SSA抑制血管生成的机制在于抑制VEGFR2以及包括PLCγ1、FAK、Src和Akt在内的下游蛋白激酶的蛋白磷酸化。总之,SSA可通过阻断VEGFR2介导的信号通路抑制血管生成和肿瘤生长。