Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/35232
Title: How Rap and its GEFs control liver physiology and cancer development. C3G alterations in human hepatocarcinoma.
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Issue Date: Jan-2018
Citation: Hepat Oncol.2018 Jan;(5)1:HEP05
Abstract: Rap proteins regulate liver physiopathology. For example, Rap2B promotes hepatocarcinoma (HCC) growth, while Rap1 might play a dual role. The RapGEF, Epac1, activates Rap upon cAMP binding, regulating metabolism, survival, and liver regeneration. A liver specific Epac2 isoform lacking cAMP-binding domain also activates Rap1, promoting fibrosis in alcoholic liver disease. C3G (RapGEF1) is also present in the liver, but mainly as shorter isoforms. Its function in the liver remains unknown. Information from different public genetic databases revealed that C3G mRNA levels increase in HCC, although they decrease in metastatic stages. In addition, several mutations in RapGEF1 gene are present, associated with a reduced patient survival. Based on this, C3G might represent a new HCC diagnostic and prognostic marker, and a therapeutic target.
PMID: 30302196
URI: https://hdl.handle.net/20.500.12530/35232
Rights: openAccess
ISSN: 2045-0923
Appears in Collections:Fundaciones e Institutos de Investigación > IIS H. U. Clínico San Carlos > Artículos

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