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Overexpression of hSav1 promotes Mst1-induced apoptosis in HeLa cells / 中华肿瘤杂志
Chinese Journal of Oncology ; (12): 481-484, 2009.
Article in Chinese | WPRIM (Western Pacific) | ID: wpr-293084
Responsible library: WPRO
ABSTRACT
<p><b>OBJECTIVE</b>To elucidate the effect of hSav1 expression on Mst1-mediated apoptosis in HeLa cells.</p><p><b>METHODS</b>Plasmids pCMV-HA-hSav1 and pcDNA/4TO-Flag-Mst1 were constructed and cotransfected into HeLa cells. Triple immunofluorescent labeling of hSav1, Mst1 and nucleus was performed to determine their subcellular localization. Plasmids pCMV-HA-hSav1 and/or pcDNA/4TO-Flag-Mst1 were transfected into HeLa cells, and 36 hours later cisplatin (50 micromol/L) as a pro-apoptotic agent was added for 14 hours. Cell apoptosis was analyzed by annexin V/PI assay.</p><p><b>RESULTS</b>Plasmids pCMV-HA-hSav1 and pcDNA/4TO-Flag-Mst1 were constructed and the authenticity of constructs was verified by sequencing. The binding in vitro showed that hSav1 could be detect from the anti-Mst1 immunoprecipitation complex. The immunofluorescent labeling showed that hSav1 and Mst1 had the same localization in cells. Overexpressed protein hSav1 did not induce a significant cell apoptosis. However, co-expression of hSav1 with Mst1 resulted in a significant increase of apoptosis above the level seen with Mst1 alone (24.5% +/- 2.4% vs. 39.3% +/- 4.0%, P < 0.05).</p><p><b>CONCLUSION</b>Our findings indicate that hSav1 is a newly identified protein that interacts with Mst1 and augments Mst1-mediated apoptosis.</p>
Subject(s)
Full text: Available Database: WPRIM (Western Pacific) Main subject: Plasmids / HeLa Cells / Transfection / Proto-Oncogene Proteins / Hepatocyte Growth Factor / Apoptosis / Cell Cycle Proteins / Cytoplasm / Genetics / Metabolism Type of study: Prognostic study Limits: Humans Language: Chinese Journal: Chinese Journal of Oncology Year: 2009 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Plasmids / HeLa Cells / Transfection / Proto-Oncogene Proteins / Hepatocyte Growth Factor / Apoptosis / Cell Cycle Proteins / Cytoplasm / Genetics / Metabolism Type of study: Prognostic study Limits: Humans Language: Chinese Journal: Chinese Journal of Oncology Year: 2009 Document type: Article
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