Department of Pharmacology, University of Colorado Anschutz Medical Campus, Aurora, CO, USA.
Cell Cycle. 2019 Dec;18(24):3421-3431. doi: 10.1080/15384101.2019.1692483. Epub 2019 Nov 18.
Autophagy is cellular recycling process that plays a complex role in cancer. Pre-clinical studies indicating a pro-tumorigenic role of autophagy have led to the launch of dozens of clinical trials combining autophagy inhibition with other standard of care therapies in different tumor types. A recent publication utilized a novel, acute, CRISPR/Cas9 assay to identify cancer cell lines that are exquisitely sensitive to loss of core autophagy genes within the first 7 days. However, weeks later, rare populations of originally autophagy dependent cells were found that could circumvent autophagy inhibition. Analysis of these rare clones revealed that in the process of circumventing loss of autophagy, the cells upregulated NRF2 signaling to maintain protein homeostasis and consequently become more sensitive to proteasome inhibition as well as knock down of NRF2. This review highlights recent publications regarding the role of autophagy in cancer and potential mechanisms cancer cells may be able to commandeer to circumvent autophagy inhibition. We hope to make significant clinical advances by understanding if and when cancer cells will become resistant to autophagy inhibition, and pre-clinical studies may be able to provide insight into the best combinatorial therapies to prevent tumor relapse while on autophagy inhibitors.
自噬是一种细胞回收过程,在癌症中起着复杂的作用。临床前研究表明自噬具有促进肿瘤发生的作用,这导致了数十项临床试验的开展,这些临床试验将自噬抑制与不同肿瘤类型的其他标准治疗方法相结合。最近的一篇出版物利用一种新颖的、急性的 CRISPR/Cas9 测定方法,鉴定出在最初的 7 天内对核心自噬基因缺失极其敏感的癌细胞系。然而,几周后,发现最初依赖自噬的稀有细胞群能够规避自噬抑制。对这些稀有克隆的分析表明,在规避自噬丧失的过程中,细胞上调了 NRF2 信号通路以维持蛋白质稳态,因此对蛋白酶体抑制以及 NRF2 敲低更为敏感。这篇综述强调了最近关于自噬在癌症中的作用以及癌细胞可能能够利用的潜在机制来规避自噬抑制的出版物。我们希望通过了解癌症细胞何时以及是否会对自噬抑制产生耐药性来取得重大的临床进展,而临床前研究可能能够为防止肿瘤复发的最佳联合治疗提供见解,同时使用自噬抑制剂。