WebDec 27, 2024 · Understanding HBx-mediated dimensions of complexity in driving liver malignancies could provide the key to unlocking novel and repurposed combinatorial therapies to combat HCC. ... It is suggested that Ct-HBx could downregulate TXNIP via a transcriptional repressor nuclear factor of activated T cells 2 (NFACT2) and serve as a … WebJul 1, 2024 · In this study, lncRNA-LOC is significantly downregulated in HCC and negatively correlated with overall survival in HCC patients. LncRNA-LOC is negatively regulated by Ct-HBx in vitro and in vivo (HCC specimens). Two novel transcripts of LncRNA-LOC in HepG2 and Huh7 cell lines were identified by 5’ and 3’ rapid amplification of cDNA ends ...
Hepatitis B virus X protein mediated epigenetic …
WebJan 11, 2024 · Huh7, Huh7/Ct-HBx (Huh7 cells expressing a carboxyl-terminal truncated form of HBx with depletion of amino acids 130–154), HepG2 and Hep3B cells were cultured in Dulbecco’s modified Eagle’s ... WebMar 1, 2015 · Hepatitis B virus X protein (HBx) is involved in the development of hepatocellular carcinoma (HCC). The HBx sequence is a preferential site of integration … dgrm horario
C-terminal truncated HBx initiates hepatocarcinogenesis by ...
WebC-terminal truncated X protein (Ct-HBx) expression can promote hepatocyte proliferation and reprogram cell metabolism by inhibiting thioredoxin-interacting protein (TXNIP). 24 Furthermore, Ct-HBx regulates the transcription of Caveolin-1 and stabilizes LRP6 to maintain the activation of β-catenin, promote the progression of HBV-associated HCC, … WebSep 3, 2013 · Ct-HBx expression in adjacent hepatic tissues significantly predicted an unfavorable RFS in the antiviral group ( P < .001). Conclusion Although it might not affect the HCC-promoting potential of Ct-HBx, NA treatment is effective in normalizing liver function, decreasing HBV-HCC recurrence, and improving postoperative survival. WebDec 5, 2024 · MC-LR combined with Ct-HBX promoted the proliferation, migration and invasion of HepG2 cells, upregulated the mRNA and protein expression of MAOA gene, and downregulated UCP2 and GPX1 genes. Conclusion: MC-LR and HBV may synergistically affect redox status and play an important role in hepatocarcinoma genesis. dgr misiones argentina