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SWI/SNF 复合物:癌症中经常发生突变的染色质重塑复合物。

The SWI/SNF Complex: A Frequently Mutated Chromatin Remodeling Complex in Cancer.

机构信息

Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.

Curriculum in Toxicology and Environmental Medicine, University of North Carolina at Chapel Hill School of Medicine, Chapel Hill, North Carolina, USA.

出版信息

Cancer Treat Res. 2023;190:211-244. doi: 10.1007/978-3-031-45654-1_7.

Abstract

The switch/sucrose non-fermenting (SWI/SNF) chromatin remodeling complex is a global regulator of gene expression known to maintain nucleosome-depleted regions at active enhancers and promoters. The mammalian SWI/SNF protein subunits are encoded by 29 genes and 11-15 subunits including an ATPase domain of either SMARCA4 (BRG1) or SMARCA2 (BRM) are assembled into a complex. Based on the distinct subunits, SWI/SNF are grouped into 3 major types (subfamilies): the canonical BRG1/BRM-associated factor (BAF/cBAF), polybromo-associated BAF (PBAF), and non-canonical BAF (GBAF/ncBAF). Pan-cancer genome sequencing studies have shown that nearly 25% of all cancers bear mutations in subunits of the SWI/SNF complex, many of which are loss of function (LOF) mutations, suggesting a tumor suppressor role. Inactivation of SWI/SNF complex subunits causes widespread epigenetic dysfunction, including increased dependence on antagonistic components such as polycomb repressor complexes (PRC1/2) and altered enhancer regulation, likely promoting an oncogenic state leading to cancer. Despite the prevalence of mutations, most SWI/SNF-mutant cancers lack targeted therapeutic strategies. Defining the dependencies created by LOF mutations in SWI/SNF subunits will identify better targets for these cancers.

摘要

SWI/SNF 染色质重塑复合物是一种已知的基因表达全局调控因子,可维持活性增强子和启动子处无核小体区域。哺乳动物 SWI/SNF 蛋白亚基由 29 个基因和 11-15 个亚基编码,其中一个 ATP 酶结构域由 SMARCA4(BRG1)或 SMARCA2(BRM)组成复合物。根据不同的亚基,SWI/SNF 分为 3 种主要类型(亚家族):经典的 BRG1/BRM 相关因子(BAF/cBAF)、多溴相关 BAF(PBAF)和非经典的 BAF(GBAF/ncBAF)。泛癌基因组测序研究表明,近 25%的所有癌症都存在 SWI/SNF 复合物亚基的突变,其中许多是功能丧失(LOF)突变,提示其作为肿瘤抑制因子的作用。SWI/SNF 复合物亚基失活会导致广泛的表观遗传功能障碍,包括对拮抗成分(如多梳抑制复合物 1/2(PRC1/2))的依赖性增加和增强子调控的改变,可能促进致癌状态导致癌症。尽管存在突变,但大多数 SWI/SNF 突变型癌症缺乏靶向治疗策略。确定 SWI/SNF 亚基 LOF 突变引起的依赖性将为这些癌症确定更好的靶点。

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