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BRM:SWI/SNF 染色质重塑复合物的核心 ATP 酶亚基——抑癌因子还是促癌因子?

BRM: the core ATPase subunit of SWI/SNF chromatin-remodelling complex-a tumour suppressor or tumour-promoting factor?

机构信息

Department of Molecular and Translational Oncology, The Maria Sklodowska-Curie Institute-Oncology Center in Warsaw, Wawelska 15B, 02-034, Warsaw, Poland.

Institute of Biochemistry and Biophysics Polish Academy of Sciences, Pawinskiego 5A, 02-106, Warsaw, Poland.

出版信息

Epigenetics Chromatin. 2019 Nov 13;12(1):68. doi: 10.1186/s13072-019-0315-4.

Abstract

BRM (BRAHMA) is a core, SWI2/SNF2-type ATPase subunit of SWI/SNF chromatin-remodelling complex (CRC) involved in various important regulatory processes including development. Mutations in SMARCA2, a BRM-encoding gene as well as overexpression or epigenetic silencing were found in various human diseases including cancer. Missense mutations in SMARCA2 gene were recently connected with occurrence of Nicolaides-Baraitser genetics syndrome. By contrast, SMARCA2 duplication rather than mutations is characteristic for Coffin-Siris syndrome. It is believed that BRM usually acts as a tumour suppressor or a tumour susceptibility gene. However, other studies provided evidence that BRM function may differ depending on the cancer type and the disease stage, where BRM may play a role in the disease progression. The existence of alternative splicing forms of SMARCA2 gene, leading to appearance of truncated functional, loss of function or gain-of-function forms of BRM protein suggest a far more complicated mode of BRM-containing SWI/SNF CRCs actions. Therefore, the summary of recent knowledge regarding BRM alteration in various types of cancer and highlighting of differences and commonalities between BRM and BRG1, another SWI2/SNF2 type ATPase, will lead to better understanding of SWI/SNF CRCs function in cancer development/progression. BRM has been recently proposed as an attractive target for various anticancer therapies including the use of small molecule inhibitors, synthetic lethality induction or proteolysis-targeting chimera (PROTAC). However, such attempts have some limitations and may lead to severe side effects given the homology of BRM ATPase domain to other ATPases, as well as due to the tissue-specific appearance of BRM- and BRG1-containing SWI/SNF CRC classes. Thus, a better insight into BRM-containing SWI/SNF CRCs function in human tissues and cancers is clearly required to provide a solid basis for establishment of new safe anticancer therapies.

摘要

BRM(Brahma)是 SWI/SNF 染色质重塑复合物(CRC)的核心 SWI2/SNF2 型 ATP 酶亚基,参与包括发育在内的各种重要调控过程。在包括癌症在内的各种人类疾病中,发现了 SMARCA2 基因突变,SMARCA2 是 BRM 编码基因,以及过度表达或表观遗传沉默。SMARCA2 基因的错义突变最近与 Nicolaides-Baraitser 遗传综合征的发生有关。相比之下,Coffin-Siris 综合征的特征是 SMARCA2 基因的重复而不是突变。人们认为 BRM 通常作为肿瘤抑制因子或肿瘤易感性基因发挥作用。然而,其他研究提供的证据表明,BRM 功能可能因癌症类型和疾病阶段而异,BRM 可能在疾病进展中发挥作用。SMARCA2 基因存在选择性剪接形式,导致截短功能、丧失功能或获得功能的 BRM 蛋白出现,这表明 BRM 含有 SWI/SNF CRC 的作用方式要复杂得多。因此,总结 BRM 在各种类型癌症中的改变,并强调 BRM 与另一种 SWI2/SNF2 型 ATP 酶 BRG1 之间的差异和共同点,将有助于更好地理解 SWI/SNF CRC 在癌症发生/进展中的作用。最近有人提出,BRM 作为各种抗癌疗法的有吸引力的靶点,包括使用小分子抑制剂、诱导合成致死或蛋白水解靶向嵌合体(PROTAC)。然而,由于 BRM ATP 酶结构域与其他 ATP 酶的同源性,以及由于含有 BRM 和 BRG1 的 SWI/SNF CRC 类在组织中的特异性出现,这些尝试存在一些限制,并可能导致严重的副作用。因此,显然需要更深入地了解 BRM 含有 SWI/SNF CRC 在人体组织和癌症中的功能,为建立新的安全抗癌疗法提供坚实的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/86d4/6852734/93a761f3df7b/13072_2019_315_Fig1_HTML.jpg

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