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STAG Mutations in Cancer

期刊

TRENDS IN CANCER
卷 5, 期 8, 页码 506-520

出版社

CELL PRESS
DOI: 10.1016/j.trecan.2019.07.001

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资金

  1. Dr Leopold and Carmen Ellinger Foundation
  2. Gert and Susanna Mayer foundation
  3. 'Verein zur Forderung von Wissenschaft und Forschung an der Medizinischen Fakultat der LMU Munchen' (WiFoMed)
  4. Mehr LEBEN fur krebskranke Kinder - Bettina-Brau-Stiftung
  5. Matthias-Lackas Foundation
  6. Friedrich-Baur foundation
  7. Dr Rolf M. Schwiete foundation
  8. Barbara and Hubertus Trettner foundation
  9. Wilhelm-Sander-Foundation [2016.167.1]
  10. Deutsche Forschungsgemeinschaft [DFG-391665916]
  11. German Cancer Aid [DKH-70112257]

向作者/读者索取更多资源

Stromal Antigen 1 and 2 (STAG1/2) are key subunits of the cohesin complex that mediate sister chromatid cohesion, DNA repair, transcriptional regulation, and genome topology. Genetic alterations comprising any of the 11 cohesin-associated genes possibly occur in up to 26% of patients included in The Cancer Genome Atlas (TCGA) studies. STAG2 shows the highest number of putative driver truncating mutations. We provide a comprehensive review of the function of STAG1/2 in human physiology and disease and an integrative analysis of available omics data on STAG alterations in a wide array of cancers, comprising 53 691 patients and 1067 cell lines. Lastly, we discuss opportunities for therapeutic intervention.

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