Sasaki Mariko, Ogiwara Hideaki
Division of Cancer Therapeutics, National Cancer Center Research Institute, 5-1-1, Tsukiji, Chuo-ku, Tokyo, 104-0045, Japan.
Sci Rep. 2024 Dec 28;14(1):31321. doi: 10.1038/s41598-024-82753-5.
Mutation of genes related to the SWI/SNF chromatin remodeling complex is detected in 20% of all cancers. The SWI/SNF chromatin remodeling complex comprises about 15 subunits and is classified into three subcomplexes: cBAF, PBAF, and ncBAF. Previously, we showed that ovarian clear cell carcinoma cells deficient in ARID1A, a subunit of the cBAF complex, are synthetic lethal with several genes required for glutathione (GSH) synthesis and are therefore sensitive to the GSH inhibitor eprenetapopt (APR-246). However, we do not know whether cancer cells deficient in SWI/SNF components other than ARID1A are selectively sensitive to treatment with eprenetapopt. Here, we show that SMARCA4-, SMARCB1-, and PBRM1-deficient cells are more sensitive to eprenetapopt than SWI/SNF-proficient cells. We found that deficiency of SMARCA4, SMARCB1, or PBRM1 attenuates transcription of the SLC7A11 gene (which supplies cysteine as a raw metabolic material for GSH synthesis) by the failure of recruitment of cBAF and PBAF to the promotor and enhancer regions of the SLC7A11 locus, thereby reducing basal levels of GSH. In addition, eprenetapopt decreased the amount of intracellular GSH and increased the intracellular amount of reactive oxygen species (ROS), followed by induction of apoptosis. Taken together, eprenetapopt could be a promising selective agent for SWI/SNF-deficient cancer cells derived from SMARCA4-deficient lung cancers, SMARCB1-deficient rhabdoid tumors, and PBRM1-deficient kidney cancers.
在所有癌症中,有20%检测到与SWI/SNF染色质重塑复合体相关的基因突变。SWI/SNF染色质重塑复合体由约15个亚基组成,分为三个亚复合体:cBAF、PBAF和ncBAF。此前,我们发现cBAF复合体的一个亚基ARID1A缺陷的卵巢透明细胞癌细胞与谷胱甘肽(GSH)合成所需的几个基因存在合成致死性,因此对GSH抑制剂依普萘妥(APR-246)敏感。然而,我们不知道除ARID1A之外的SWI/SNF组分缺陷的癌细胞是否对依普萘妥治疗具有选择性敏感性。在此,我们表明,与SWI/SNF功能正常的细胞相比,SMARCA4、SMARCB1和PBRM1缺陷的细胞对依普萘妥更敏感。我们发现,SMARCA4、SMARCB1或PBRM1的缺陷会导致cBAF和PBAF无法募集到SLC7A11基因座的启动子和增强子区域,从而减弱SLC7A11基因(为GSH合成提供半胱氨酸作为代谢原料)的转录,进而降低GSH的基础水平。此外,依普萘妥减少了细胞内GSH的量,增加了细胞内活性氧(ROS)的量,随后诱导细胞凋亡。综上所述,依普萘妥可能是一种有前景的选择性药物,用于治疗源自SMARCA4缺陷型肺癌、SMARCB1缺陷型横纹肌肉瘤和PBRM1缺陷型肾癌的SWI/SNF缺陷型癌细胞。