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STAG Mutations in Cancer.
Romero-Pérez, Laura; Surdez, Didier; Brunet, Erika; Delattre, Olivier; Grünewald, Thomas G P.
Afiliación
  • Romero-Pérez L; Max-Eder Research Group for Pediatric Sarcoma Biology, Institute of Pathology, Faculty of Medicine, LMU, Munich, Germany.
  • Surdez D; INSERM U830, Équipe Labellisé LNCC "Genetics and Biology of Pediatric Cancers", fhna PSL Université, SIREDO Oncology Centre, Institut Curie, Paris, France.
  • Brunet E; Institut Imagine, INSERM UMR1163, Équipe Labellisé LNCC, Dynamics of the Genome and Immune System Lab, Paris, France.
  • Delattre O; INSERM U830, Équipe Labellisé LNCC "Genetics and Biology of Pediatric Cancers", fhna PSL Université, SIREDO Oncology Centre, Institut Curie, Paris, France.
  • Grünewald TGP; Max-Eder Research Group for Pediatric Sarcoma Biology, Institute of Pathology, Faculty of Medicine, LMU, Munich, Germany; Institute of Pathology, Faculty of Medicine, LMU Munich, Munich, Germany; German Cancer Consortium (DKTK), partner site Munich, Munich, Germany; German Cancer Research Center (DK
Trends Cancer ; 5(8): 506-520, 2019 08.
Article en En | MEDLINE | ID: mdl-31421907
ABSTRACT
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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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Nucleares / Proteínas Cromosómicas no Histona / Proteínas de Ciclo Celular / Carcinogénesis / Neoplasias Límite: Humans Idioma: En Revista: Trends Cancer Año: 2019 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Proteínas Nucleares / Proteínas Cromosómicas no Histona / Proteínas de Ciclo Celular / Carcinogénesis / Neoplasias Límite: Humans Idioma: En Revista: Trends Cancer Año: 2019 Tipo del documento: Article País de afiliación: Alemania