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[染色质重塑缺陷与癌症:SWI/SNF 实例]

[Chromatin remodeling defects and cancer: the SWI/SNF example].

作者信息

Bourdeaut Franck, Bièche Ivan

机构信息

Institut Curie, département d'oncologie pédiatrique, Inserm U830-laboratoire de génétique et biologie des cancers, 26, rue d'Ulm, 75248 Paris Cedex 05, France.

出版信息

Bull Cancer. 2012 Dec;99(12):1133-40. doi: 10.1684/bdc.2012.1664.

Abstract

The SWI/SNF complex is a multiprotein complex essential for chromatin remodelling. As such, it plays a key role in the epigenetic regulation of genome expression. This complex is composed of a dozen of proteins, some of which are constant and ubiquitous, especially SMARCB1 and SMARCA4. Mutations in these genes are now described in an increasing number of tumors. Mutations in SMARCB1 characterize the majority of rhabdoid tumors, an aggressive malignancy that exquisitely depends on this single genetic event. Rare rhabdoid tumors have mutation in SMARCA4, a genetic abnormality also found in some medulloblastomas. Many other tumor types, of variable aggressiveness, show an abnormal loss of expression of SMARCB1, but the genetic underlying cause most often remains elusive. The recent sequencings of whole exomes have described frequent mutations in other genes of the SWI/SNF complex: mutations in ARID1A in liver, gastric or bladder carcinomas, and PBRM1 mutations in renal cancers. These data establish the wide role of SWI/SNF complex in cancers and justify that major efforts should now be devoted to this common mechanism of human oncogenesis.

摘要

SWI/SNF复合物是一种对染色质重塑至关重要的多蛋白复合物。因此,它在基因组表达的表观遗传调控中起着关键作用。该复合物由十几种蛋白质组成,其中一些是恒定且普遍存在的,尤其是SMARCB1和SMARCA4。现在越来越多的肿瘤中发现了这些基因的突变。SMARCB1突变是大多数横纹肌样肿瘤的特征,横纹肌样肿瘤是一种侵袭性恶性肿瘤,完全依赖于这一单一基因事件。罕见的横纹肌样肿瘤有SMARCA4突变,这种基因异常在一些髓母细胞瘤中也有发现。许多其他侵袭性各异的肿瘤类型显示出SMARCB1表达异常缺失,但最常见的遗传潜在原因仍然难以捉摸。最近的全外显子测序描述了SWI/SNF复合物其他基因的频繁突变:肝癌、胃癌或膀胱癌中的ARID1A突变,以及肾癌中的PBRM1突变。这些数据证实了SWI/SNF复合物在癌症中的广泛作用,并表明现在应该大力致力于研究这种人类肿瘤发生的常见机制。

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