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Effect of Hepatocyte Growth Factor (Hgf) on the Level of Survivin & Xiap Expression in Several Human Cancer Cell Lines, After Treating With Dna Damaging Agent Publisher Pubmed



Keyhanian K1, 2, 3 ; Edalat R2 ; Oghalaei A4 ; Askary N2 ; Golshani A3 ; Salehi M5 ; Sarramiforooshani R2 ; Shokrgozar MA1
Authors
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Authors Affiliations
  1. 1. National Cell Bank of Iran, Pasteur Institute of Iran, Tehran, Iran
  2. 2. HIV Unit, Department of Biotechnology, Pasteur Institute of Iran, Tehran, Iran
  3. 3. Medical Students Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran
  4. 4. H-pylori Unit, Department of Biotechnology, Pasteur Institute of Iran, Tehran, Iran
  5. 5. Department of Genetics and Molecular Biology, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran

Source: Molecular and Cellular Biochemistry Published:2007


Abstract

Hepatocyte growth factor (HGF) has opposite biological activities in regulating apoptosis, also underlying molecular mechanisms are not clearly defined. We investigated HGF ability to inhibit cell death, which was induced by Doxorubicin, a DNA damaging agent. Also Survivin and XIAP mRNA levels were compared in HGF treated and non-treated cells. Cell proliferation and death were assessed using MTT assay and dye exclusion tests. Quantitative real-time PCR was used to evaluate Survivin and XIAP expression levels after treatment with HGF. ELISA was performed to quantify HGF secretion in the selected cancer cell lines media. HGF appeared to have inhibitory effect on Doxorubicin induced cell death in all of the studied cell lines. It had minimal effect on XAIP and Survivin expression levels in MRC-5, MOLT-4 and AGS cell lines; except for XIAP expression level in AGS cell line, which was increased substantially after treatment. Surprisingly, in KG-1 cell line, XIAP and Survivin expression levels were significantly reduced after HGF treatment. Although several members of IAP gene family are reported to play role in HGF mediated cytoprotective pathway, we showed that XIAP and Survivin do not seem to be involved. © Springer Science+Business Media, LLC 2007.