Division of Genome Biology, National Cancer Center Research Institute, 5-1-1, Tsukiji, Chuo-ku, Tokyo 104-0045, Japan.
Division of Genome Biology, National Cancer Center Research Institute, 5-1-1, Tsukiji, Chuo-ku, Tokyo 104-0045, Japan; Department of Obstetrics and Gynecology, The Jikei University School of Medicine, 3-25-8 Nishi-Shinbashi, Minato-ku, Tokyo 105-8461, Japan.
Cancer Cell. 2019 Feb 11;35(2):177-190.e8. doi: 10.1016/j.ccell.2018.12.009. Epub 2019 Jan 24.
ARID1A encodes an SWI/SNF chromatin-remodeling factor and is frequently mutated in various cancers. This study demonstrates that ARID1A-deficient cancer cells are specifically vulnerable to inhibition of the antioxidant glutathione (GSH) and the glutamate-cysteine ligase synthetase catalytic subunit (GCLC), a rate-limiting enzyme for GSH synthesis. Inhibition of GCLC markedly decreased GSH in ARID1A-deficient cancer cells, leading to apoptotic cell death triggered by excessive amounts of reactive oxygen species. The vulnerability of ARID1A-deficient cancer cells results from low basal levels of GSH due to impaired expression of SLC7A11. The SLC7A11-encoded cystine transporter supplies cells with cysteine, a key source of GSH, and its expression is enhanced by ARID1A-mediated chromatin remodeling. Thus, ARID1A-deficient cancers are susceptible to synthetic lethal targeting of GCLC.
ARID1A 编码一个 SWI/SNF 染色质重塑因子,并且在多种癌症中经常发生突变。本研究表明,ARID1A 缺陷的癌细胞对抗氧化谷胱甘肽 (GSH) 和谷氨酸-半胱氨酸连接酶合成酶催化亚基 (GCLC) 的抑制特别敏感,后者是 GSH 合成的限速酶。GCLC 的抑制显著降低了 ARID1A 缺陷的癌细胞中的 GSH,导致过量活性氧物质引发的细胞凋亡。由于 SLC7A11 表达受损,导致 ARID1A 缺陷的癌细胞中 GSH 的基础水平较低,从而导致其易受损伤。SLC7A11 编码的胱氨酸转运蛋白为细胞提供半胱氨酸,这是 GSH 的关键来源,其表达可通过 ARID1A 介导的染色质重塑得到增强。因此,ARID1A 缺陷的癌症容易受到 GCLC 的合成致死靶向作用的影响。