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JCR 2016
جستجوی مقالات
چهارشنبه 17 دی 1404
Avicenna Journal of Medical Biotechnology
، جلد ۶، شماره ۱، صفحات ۳-۹
عنوان فارسی
چکیده فارسی مقاله
کلیدواژههای فارسی مقاله
عنوان انگلیسی
Effect of Hepatitis B Virus X Gene on the Expression Level of p53 Gene using Hep G2 Cell Line
چکیده انگلیسی مقاله
Background: The HBV-X (HBX) protein is believed to contribute to the development of HCC. However, the molecular mechanisms involved in HBX-mediated hepatocarcinogenesis remain obscure. In this study, the effect of hepatitis B virus X gene and its protein product HBxAg on expression of p53 gene in Hep G2 cell line was investigated. Methods: Viral DNA extracted from HBV-positive serum and HBX gene region was amplified using polymerase chain reaction (PCR). Then, PCR product was cloned into the pcDNA3 vector. After confirmation of cloning, the recombinant plasmid pcDNA3-X was transfected into HepG2 cell line using lipid-mediated DNA-transfection procedure. SDS-PAGE and western blotting methods were used to identify expression of HBX protein. Relative quantification was used to analyze the p53gene expression using the 2-ΔΔ Ct method. Results: Recombinant plasmid pcDNA3–HBX was confirmed by restriction endonucleases digestion and colony-PCR. The results of SDS-PAGE and western blot assays showed that HBX gene could be expressed in Hep G2 cell line. There was no significant difference between the expression levels of p53 compared with GAPDH gene as housekeeping gene (p< 0.05). Conclusion: There was no significant difference in the protein levels between the transfected cells with X gene containing HBX130 and HBX131 double mutations and p53 gene. It is necessary to do more studies on Hepatitis B virus to understand the role of HBX on the development of liver cancer and its function on p53 tumor suppressor protein.
کلیدواژههای انگلیسی مقاله
Hepatitis B virus, Hep G2 cell line, p53 gene, X gene
نویسندگان مقاله
نشانی اینترنتی
http://www.ajmb.org/En/Article.aspx?id=136
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اشکال در دسترسی به فایل - ./files/site1/rds_journals/133/article-133-376120.pdf
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en
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