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
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2016年 / 1866卷 / 01期
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
相关论文
共 86 条
  • [1] [Anonymous], TUMOUR BIOL
  • [2] Glioblastoma Cells Containing Mutations in the Cohesin Component STAG2 Are Sensitive to PARP Inhibition
    Bailey, Melanie L.
    O'Neil, Nigel J.
    van Pel, Derek M.
    Solomon, David A.
    Waldman, Todd
    Hieter, Philip
    [J]. MOLECULAR CANCER THERAPEUTICS, 2014, 13 (03) : 724 - 732
  • [3] Recurrent inactivation of STAG2 in bladder cancer is not associated with aneuploidy
    Balbas-Martinez, Cristina
    Sagrera, Ana
    Carrillo-de-Santa-Pau, Enrique
    Earl, Julie
    Marquez, Mirari
    Vazquez, Miguel
    Lapi, Eleonora
    Castro-Giner, Francesc
    Beltran, Sergi
    Bayes, Monica
    Carrato, Alfredo
    Cigudosa, Juan C.
    Dominguez, Orlando
    Gut, Marta
    Herranz, Jesus
    Juanpere, Nuria
    Kogevinas, Manolis
    Langa, Xavier
    Lopez-Knowles, Elena
    Lorente, Jose A.
    Lloreta, Josep
    Pisano, David G.
    Richart, Laia
    Rico, Daniel
    Salgado, Rocio N.
    Tardon, Adonina
    Chanock, Stephen
    Heath, Simon
    Valencia, Alfonso
    Losada, Ana
    Gut, Ivo
    Malats, Nuria
    Real, Francisco X.
    [J]. NATURE GENETICS, 2013, 45 (12) : 1464 - U221
  • [4] Chromatid cohesion defects may underlie chromosome instability in human colorectal cancers
    Barber, Thomas D.
    McManus, Kirk
    Yuen, Karen W. Y.
    Reis, Marcelo
    Parmigiani, Giovanni
    Shen, Dong
    Barrett, Irene
    Nouhi, Yasaman
    Spencer, Forrest
    Markowitz, Sanford
    Velculescu, Victor E.
    Kinzler, Kenneth W.
    Vogelstein, Bert
    Lengauer, Christoph
    Hieter, Philip
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (09) : 3443 - 3448
  • [5] CLONING AND CHARACTERIZATION OF RAD21 AN ESSENTIAL GENE OF SCHIZOSACCHAROMYCES-POMBE INVOLVED IN DNA DOUBLE-STRAND-BREAK REPAIR
    BIRKENBIHL, RP
    SUBRAMANI, S
    [J]. NUCLEIC ACIDS RESEARCH, 1992, 20 (24) : 6605 - 6611
  • [6] Cornelia de Lange syndrome
    Boyle, M. I.
    Jespersgaard, C.
    Brondum-Nielsen, K.
    Bisgaard, A. -M.
    Tumer, Z.
    [J]. CLINICAL GENETICS, 2015, 88 (01) : 1 - 12
  • [7] The Somatic Genomic Landscape of Glioblastoma
    Brennan, Cameron W.
    Verhaak, Roel G. W.
    McKenna, Aaron
    Campos, Benito
    Noushmehr, Houtan
    Salama, Sofie R.
    Zheng, Siyuan
    Chakravarty, Debyani
    Sanborn, J. Zachary
    Berman, Samuel H.
    Beroukhim, Rameen
    Bernard, Brady
    Wu, Chang-Jiun
    Genovese, Giannicola
    Shmulevich, Ilya
    Barnholtz-Sloan, Jill
    Zou, Lihua
    Vegesna, Rahulsimham
    Shukla, Sachet A.
    Ciriello, Giovanni
    Yung, W. K.
    Zhang, Wei
    Sougnez, Carrie
    Mikkelsen, Tom
    Aldape, Kenneth
    Bigner, Darell D.
    Van Meir, Erwin G.
    Prados, Michael
    Sloan, Andrew
    Black, Keith L.
    Eschbacher, Jennifer
    Finocchiaro, Gaetano
    Friedman, William
    Andrews, David W.
    Guha, Abhijit
    Iacocca, Mary
    O'Neill, Brian P.
    Foltz, Greg
    Myers, Jerome
    Weisenberger, Daniel J.
    Penny, Robert
    Kucherlapati, Raju
    Perou, Charles M.
    Hayes, D. Neil
    Gibbs, Richard
    Marra, Marco
    Mills, Gordon B.
    Lander, Eric
    Spellman, Paul
    Wilson, Richard
    [J]. CELL, 2013, 155 (02) : 462 - 477
  • [8] The Genomic Landscape of the Ewing Sarcoma Family of Tumors Reveals Recurrent STAG2 Mutation
    Brohl, Andrew S.
    Solomon, David A.
    Chang, Wendy
    Wang, Jianjun
    Song, Young
    Sindiri, Sivasish
    Patidar, Rajesh
    Hurd, Laura
    Chen, Li
    Shern, Jack F.
    Liao, Hongling
    Wen, Xinyu
    Gerard, Julia
    Kim, Jung-Sik
    Lopez Guerrero, Jose Antonio
    Machado, Isidro
    Wai, Daniel H.
    Picci, Piero
    Triche, Timothy
    Horvai, Andrew E.
    Miettinen, Markku
    Wei, Jun S.
    Catchpool, Daniel
    Llombart-Bosch, Antonio
    Waldman, Todd
    Khan, Javed
    [J]. PLOS GENETICS, 2014, 10 (07):
  • [9] APRIN is a cell cycle specific BRCA2-interacting protein required for genome integrity and a predictor of outcome after chemotherapy in breast cancer
    Brough, Rachel
    Bajrami, Ilirjana
    Vatcheva, Radost
    Natrajan, Rachael
    Reis-Filho, Jorge S.
    Lord, Christopher J.
    Ashworth, Alan
    [J]. EMBO JOURNAL, 2012, 31 (05) : 1160 - 1176
  • [10] Differential regulation of telomere and centromere cohesion by the Scc3 homologues SA1 and SA2, respectively, in human cells
    Canudas, Silvia
    Smith, Susan
    [J]. JOURNAL OF CELL BIOLOGY, 2009, 187 (02) : 165 - 173