Department of Immunology, School of Basic Medical Sciences, Hubei University of Medicine, 442000, Shiyan, Hubei, P. R. China.
Hubei Key Laboratory of Embryonic Stem Cell Research, Hubei University of Medicine, 442000, Shiyan, Hubei, P. R. China.
Cell Death Dis. 2021 May 7;12(5):457. doi: 10.1038/s41419-021-03722-8.
Colorectal cancer (CRC) is one of the most aggressive and lethal cancers. The role of autophagy in the pathobiology of CRC is intricate, with opposing functions manifested in different cellular contexts. The Yes-associated protein (YAP), a transcriptional coactivator inactivated by the Hippo tumor-suppressor pathway, functions as an oncoprotein in a variety of cancers. In this study, we found that YAP could negatively regulate autophagy in CRC cells, and consequently, promote tumor progression of CRC in vitro and in vivo. Mechanistically, YAP interacts with TEAD forming a complex to upregulate the transcription of the apoptosis-inhibitory protein Bcl-2, which may subsequently facilitate cell survival by suppressing autophagy-related cell death; silencing Bcl-2 expression could alleviate YAP-induced autophagy inhibition without affecting YAP expression. Collectively, our data provide evidence for YAP/Bcl-2 as a potential therapeutic target for drug exploration against CRC.
结直肠癌(CRC)是最具侵袭性和致命性的癌症之一。自噬在 CRC 的病理生物学中的作用错综复杂,在不同的细胞环境中表现出相反的功能。Yes 相关蛋白(YAP)是 Hippo 肿瘤抑制途径失活的转录共激活因子,在多种癌症中作为癌蛋白发挥作用。在本研究中,我们发现 YAP 可负向调节 CRC 细胞中的自噬,从而促进 CRC 在体外和体内的肿瘤进展。从机制上讲,YAP 与 TEAD 相互作用形成复合物,上调凋亡抑制蛋白 Bcl-2 的转录,这可能通过抑制自噬相关细胞死亡来促进细胞存活;沉默 Bcl-2 的表达可以减轻 YAP 诱导的自噬抑制,而不影响 YAP 的表达。总之,我们的数据为 YAP/Bcl-2 作为针对 CRC 的药物探索的潜在治疗靶点提供了证据。