Cohesin mutations in human cancer

被引:91
|
作者
Hill, Victoria K. [1 ]
Kim, Jung-Sik [1 ]
Waldman, Todd [1 ]
机构
[1] Georgetown Univ, Sch Med, Lombardi Comprehens Canc Ctr, 3970 Reservoir Rd NW,NRB E304, Washington, DC 20057 USA
来源
关键词
Cohesin; Cancer; STAG2; Urothelial carcinoma; Ewing sarcoma; Myeloid malignancy; SISTER-CHROMATID COHESION; DE-LANGE-SYNDROME; GENOMIC LANDSCAPE; BLADDER-CANCER; WHOLE-GENOME; STAG2; GENES; COMPLEX; ANEUPLOIDY; TUMORIGENESIS;
D O I
10.1016/j.bbcan.2016.05.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cohesin is a highly-conserved protein complex that plays important roles in sister chromatid cohesion, chromatin structure, gene expression, and DNA repair. In humans, cohesin is a ubiquitously expressed, multi-subunit protein complex composed of core subunits SMC1A, SMC3, RAD21, STAG1/2 and regulatory subunits WAPL, PDS5A/B, CDCA5, NIPBL, and MAU2. Recent studies have demonstrated that genes encoding cohesin subunits are somatically mutated in a wide range of human cancers. STAG2 is the most commonly mutated subunit, and in a recent analysis was identified as one of only 12 genes that are significantly mutated in four or more cancer types. In this review we summarize the findings reported to date and comment on potential functional implications of cohesin mutation in the pathogenesis of human cancer. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:1 / 11
页数:11
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