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GATA3 and APOBEC3B are prognostic markers in adrenocortical carcinoma and APOBEC3B is directly transcriptionally regulated by GATA3.
Gara, Sudheer Kumar; Tyagi, Monica Varun; Patel, Dhaval Thakkur; Gaskins, Kelli; Lack, Justin; Liu, Yi; Kebebew, Electron.
Afiliação
  • Gara SK; Thoracic Surgery Branch, National Cancer Institute, National Institutes of Health, Bethesda, MD, USA.
  • Tyagi MV; These authors contributed equally to this work & are first authors.
  • Patel DT; The Department of Surgery and Stanford Cancer Institute, Stanford University, Stanford, CA, USA.
  • Gaskins K; These authors contributed equally to this work & are first authors.
  • Lack J; Department of Surgery, Medical College of Wisconsin, Milwaukee, WI, USA.
  • Liu Y; Office of Science and Technology Resources, Frederick National Laboratory for Cancer Research, National Institutes of Health, Bethesda, MD, USA.
  • Kebebew E; Office of Science and Technology Resources, Frederick National Laboratory for Cancer Research, National Institutes of Health, Bethesda, MD, USA.
Oncotarget ; 11(36): 3354-3370, 2020 Sep 08.
Article em En | MEDLINE | ID: mdl-32934779
ABSTRACT
Recent evidence has implicated APOBEC3B (Apolipoprotein B mRNA editing enzyme catalytic subunit 3B) as a source of mutations in breast, bladder, cervical, lung, head, and neck cancers. However, the role of APOBEC3B in adrenocortical carcinoma (ACC) and the mechanisms through which its expression is regulated in cancer are not fully understood. Here, we report that APOBEC3B is overexpressed in ACC and it regulates cell proliferation by inducing S phase arrest. We show high APOBEC3B expression is associated with a higher copy number gain/loss at chromosome 4 and 8 and TP53 mutation rate in ACC. GATA3 was identified as a positive regulator of APOBEC3B expression and directly binds the APOBEC3B promoter region. Both GATA3 and APOBEC3B expression levels were associated with patient survival. Our study provides novel insights into the function and regulation of APOBEC3B expression in addition to its known mutagenic ability.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article