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Telomerase Activity and Telomerase Reverse Transcriptase Expression Induced by Selenium in Rat Hepatocytes 被引量:2

Telomerase Activity and Telomerase Reverse Transcriptase Expression Induced by Selenium in Rat Hepatocytes
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摘要 Objective To investigate the effects of sodium selenite on telomerase activity, apoptosis and expression of TERT, c-myc and p53 in rat hepatocytes. Methods Selenium at doses of 2.5, 5.0, and 10 μmol/kg was given to SD rats by garage. In rat hepatocytes, telomerase activity was measured by the telomeric repeat amplification protocol (TRAP), apoptosis was detected by flow cytometry, and expressions of telomerase reverse transcriptase (TERT), c-myc and p53 were analyzed by reverse transcription-polymerase chain reaction (RT-PCR). c-Myc and P53 proteins were detected by immunochemistry. Results Selenium at doses of 2.5, 5.0, and 10 μmol/kg significantly increased hepatocellular telomerase activity and induced apoptosis in a dose-dependent manner. Although selenium at doses of 2.5, 5.0, and 10 μmol/kg displayed no obvious enhancing effect on the TERT mRNA expression in rat hepatocytes (P〉0.05), it significantly increased the c-myc mRNA and p53 mRNA expression at the dose of 10 μmol/kg (P〈0.05). Selenium at doses of 5.0 and 10 μmol/kg obviously increased the content of P53 protein in rat hepatocytes, but only at the dose of 10 μmol/kg, it significantly promoted the value of c-Myc protein in them. Conclusion Selenium can slightly increase telomerase activity and TERT expression, and significantly induce apoptosis and over-expression of c-myc and p53 at relatively high doses. The beneficial effects of selenium on senescence and aging may be mediated by telomerase activation and expression of TERT, c-myc, and p53 in rat hepatocytes. Objective To investigate the effects of sodium selenite on telomerase activity, apoptosis and expression of TERT, c-myc and p53 in rat hepatocytes. Methods Selenium at doses of 2.5, 5.0, and 10 μmol/kg was given to SD rats by garage. In rat hepatocytes, telomerase activity was measured by the telomeric repeat amplification protocol (TRAP), apoptosis was detected by flow cytometry, and expressions of telomerase reverse transcriptase (TERT), c-myc and p53 were analyzed by reverse transcription-polymerase chain reaction (RT-PCR). c-Myc and P53 proteins were detected by immunochemistry. Results Selenium at doses of 2.5, 5.0, and 10 μmol/kg significantly increased hepatocellular telomerase activity and induced apoptosis in a dose-dependent manner. Although selenium at doses of 2.5, 5.0, and 10 μmol/kg displayed no obvious enhancing effect on the TERT mRNA expression in rat hepatocytes (P〉0.05), it significantly increased the c-myc mRNA and p53 mRNA expression at the dose of 10 μmol/kg (P〈0.05). Selenium at doses of 5.0 and 10 μmol/kg obviously increased the content of P53 protein in rat hepatocytes, but only at the dose of 10 μmol/kg, it significantly promoted the value of c-Myc protein in them. Conclusion Selenium can slightly increase telomerase activity and TERT expression, and significantly induce apoptosis and over-expression of c-myc and p53 at relatively high doses. The beneficial effects of selenium on senescence and aging may be mediated by telomerase activation and expression of TERT, c-myc, and p53 in rat hepatocytes.
出处 《Biomedical and Environmental Sciences》 SCIE CAS CSCD 2009年第4期311-317,共7页 生物医学与环境科学(英文版)
基金 supported by the Scientific Foundation and Teacher’s Foundation of Guangdong Pharmaceutical University (No.2006GGW01) the National Natural Science Foundation of China (No.30271110)
关键词 SELENIUM TELOMERASE Telomerase reverse transcriptase C-MYC P53 Selenium Telomerase Telomerase reverse transcriptase c-myc p53
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  • 1AI-GuoWANG,TAOXIA,QI-LONGCHU,MINGZHANG,FANGLIU,XUE-MINCHEN,KE-DIYANG.Effects of Fluoride on Lipid Peroxidation, DNA Damage and Apoptosis in Human Embryo Hepatocytes[J].Biomedical and Environmental Sciences,2004,17(2):217-222. 被引量:18
  • 2Nakamura TM;Morin GB;Chapman KB.Telomerase catalytic subunit homologs from fission yeast and human[J],1997(5328).
  • 3Greenberg RA;O'Hagan RC;Deng H.Telomerase reverse tran scriptase gene is a direct target of c-myc but is not functionally e quivalent in cellular transformation[J],1999(5).
  • 4Arinaga M;Shimizu S;Gotoh K.Expression of human telomerase subunit genes in primary lung cancer and its clinical significance[J],2000(2).
  • 5Ivan B;Catherine N;Paradis V.Quantitation of hTERT gene expression in sporadic breast tumors with a real-time reverse transcription-polymerase chain reaction assay[J],2000.
  • 6Latil A;Vidaud D;Valeri A.hTERT expression correlates with myc over-expression in human prostate cancer[J],2000.
  • 7Hahn WC;Counter CM;Lundberg AS.Creation of human tumour cells with defined genetic elements[J],1999(6743).
  • 8Taga S;Osaki T;Ohgami A.Prognostic impact of telomerase activity in non-small cell lung cancers[J],1999(5).
  • 9OH S;Song YH;Kim UJ.In vivo and in vitro analyses of myc for differential promoter activities of the human telomerase (hTERT) gene in normal and tumor cells[J],1999.
  • 10Kim HS;Shin JY;Yun JY.Immortalization of human embryonic fibroblasts by overexpression of c-myc and simian virus 40 large T antigen,2001.

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