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10.3892/br.2017.894

http://scihub22266oqcxt.onion/10.3892/br.2017.894
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C5449961!5449961!28584639
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suck abstract from ncbi


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pmid28584639      Biomed+Rep 2017 ; 6 (6): 671-4
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  • The evaluation of fibrotic effects of the hepatitis B virus pre-core in hepatic stellate cells #MMPMID28584639
  • Hosseini SY; Baesi K; Azarpira N; Pakneiat A; Hosseini SA
  • Biomed Rep 2017[Jun]; 6 (6): 671-4 PMID28584639show ga
  • The role of the hepatitis B virus (HBV) endogenous pre-core protein in liver fibrosis is controversial. Whether the expression of the pre-core induces the activation of human stellate cells (HSCs) has not yet been reported. Plasmids expressing HBx, or pre-core protein were transfected into LX-2 cells. Subsequently, total RNA extracted and reverse transcription-quantitative polymerase chain reaction was performed to measure the fold change of collagen type I, ?1 chain, ?-smooth muscle actin and TIMP metalloproteinase inhibitor-1. Moreover, transforming growth factor (TGF)-? in the supernatant of HSCs was evaluated by ELISA assay. In addition, a MTT assay was performed to test the cytotoxicity of the endogenous expression in LX-2 cells. None of the plasmids exhibited cytotoxic nor significant proliferative effects on LX-2 cells by MTT assessment. The gene expression analysis of fibrotic genes in LX-2 cells demonstrated that the pre-core protein presented no significant (P>0.05) fibrotic impact when compared to the empty control plasmid and HBx. The data from the TGF-? ELISA was consistent with the mRNA expression as detected with the control plasmid (P>0.05). The endogenous expression of the HBV pre-core exhibited no fibrotic impression in HSCs when compared to HBx.
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