Department of Integrative Medicine, Huashan Hospital, Fudan University, Shanghai, PR China.
Institutes of Integrative Medicine, Fudan University, Shanghai, PR China.
Int J Biol Sci. 2019 Jun 2;15(7):1500-1513. doi: 10.7150/ijbs.33146. eCollection 2019.
Non-small cell lung cancer (NSCLC) is the leading cause of cancer death in the world. Inhibitor of differentiation 1 (Id1) is overexpressed in NSCLC and involved in promoting its progression and metastasis. Identifying natural compounds targeting Id1 may have utility in NSCLC treatment. Here, we sought to determine whether the anti-tumor activities of flavonoids (SFs) were related to Id1. We reported that three SFs (baicalin, baicalein and wogonin) exhibited strong antitumor activity in NSCLC cells and Id1 played a pivotal role on blockage of migration and invasion by SFs. Abrogation of invasion and migration mediated by baicalin, baicalein and wogonin were totally abolished by ectopic overexpression of Id1. Mechanistically, baicalin, baicalein and wogonin activated Rap1-GTP binding and dephosphorylated Akt and Src by suppressing a7nAChR, consequently triggering inhibition of Id1. Then attenuation of its downstream mediators, VEGF-A, N-cadherin, vimentin, combined with augment of E-cadherin led to the blockage of proliferation, EMT and angiogenesis of NSCLC. Overall, our data shed light on heretofore-undescribed role of SFs as modulators of Id1, which may be a useful strategy in the treatment of NSCLC.
非小细胞肺癌(NSCLC)是全球癌症死亡的主要原因。抑制剂分化 1(Id1)在 NSCLC 中过度表达,并参与促进其进展和转移。鉴定针对 Id1 的天然化合物可能对 NSCLC 的治疗具有实用价值。在这里,我们试图确定黄酮类化合物(SFs)的抗肿瘤活性是否与 Id1 有关。我们报道了三种 SFs(黄芩素、黄芩素和白杨素)在 NSCLC 细胞中表现出强烈的抗肿瘤活性,并且 Id1 在 SFs 阻断迁移和侵袭中起关键作用。Id1 的异位过表达完全消除了黄芩素、黄芩素和白杨素介导的侵袭和迁移。在机制上,黄芩素、黄芩素和白杨素通过抑制 a7nAChR 激活 Rap1-GTP 结合并使 Akt 和 Src 去磷酸化,从而抑制 Id1。随后,其下游介质 VEGF-A、N-钙粘蛋白、波形蛋白的衰减,与 E-钙粘蛋白的增加相结合,导致 NSCLC 的增殖、EMT 和血管生成受阻。总的来说,我们的数据揭示了 SFs 作为 Id1 调节剂的以前未描述的作用,这可能是治疗 NSCLC 的一种有用策略。