| Literature DB >> 30686770 |
Hideaki Ogiwara1, Kazuaki Takahashi2, Mariko Sasaki3, Takafumi Kuroda2, Hiroshi Yoshida4, Reiko Watanabe4, Ami Maruyama5, Hideki Makinoshima6, Fumiko Chiwaki7, Hiroki Sasaki7, Tomoyasu Kato8, Aikou Okamoto9, Takashi Kohno10.
Abstract
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.Entities:
Keywords: APR-246; ARID1A; GCLC; SWI/SNF chromatin-remodeling complex; glutathione; ovarian cancer; ovarian clear cell carcinoma; reactive oxygen species; synthetic lethality; vulnerability
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Year: 2019 PMID: 30686770 DOI: 10.1016/j.ccell.2018.12.009
Source DB: PubMed Journal: Cancer Cell ISSN: 1535-6108 Impact factor: 31.743