Please use this identifier to cite or link to this item: http://ahro.austin.org.au/austinjspui/handle/1/11106
Title: The C-terminal flanking peptide (CTFP) of progastrin inhibits apoptosis via a PI3-kinase-dependent pathway.
Authors: Patel, Oneel;Marshall, Kathryn M;Bramante, Gianni;Baldwin, Graham S;Shulkes, Arthur
Affiliation: Department of Surgery, University of Melbourne Austin Health, Melbourne, Victoria 3084, Australia.
Issue Date: 19-Aug-2010
Citation: Regulatory Peptides 2010; 165(2-3): 224-31
Abstract: Progastrin is processed to a number of peptides including glycine-extended gastrin, amidated gastrin and the C-terminal flanking peptide (CTFP). Progastrin and gastrin-gly are pro-proliferative and anti-apoptotic in gastric and colorectal cancer cell lines. The CTFP is a major form of progastrin in the stomach and colon and stimulates proliferation. However the effect of CTFP on apoptosis has not been examined. Using the human gastric carcinoma cell line AGS we show that CTFP attenuates apoptosis through a PI3-kinase pathway by stimulating the phosphorylation of Akt leading to sustained increases in the concentrations of Bcl-xL and phosphorylated Bad protein and by reducing caspase 3 activity. The anti-apoptotic effect represents an important potential mechanism for the growth promoting action of CTFP.
Internal ID Number: 20727916
URI: http://ahro.austin.org.au/austinjspui/handle/1/11106
DOI: 10.1016/j.regpep.2010.08.005
URL: http://www.ncbi.nlm.nih.gov/pubmed/20727916
Type: Journal Article
Subjects: Apoptosis.drug effects
Blotting, Western
Cell Line, Tumor
Cell Survival.drug effects
Flow Cytometry
Gastrins.chemistry
Humans
Peptide Fragments.chemistry.pharmacology
Phosphatidylinositol 3-Kinases.metabolism
Protein Precursors.chemistry
Signal Transduction.drug effects
Appears in Collections:Journal articles

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