Gastroenterology Unit, IRCCS Casa Sollievo della Sofferenza Hospital, San Giovanni Rotondo (FG), Italy.
FEBS Lett. 2013 May 2;587(9):1424-8. doi: 10.1016/j.febslet.2013.03.021. Epub 2013 Mar 21.
Hepatitis delta virus (HDV) is a small, defective RNA virus that can infect only individuals carrying hepatitis B virus. HBV/HDV co-infection results in more severe liver disease than HBV single infection and more rapid progression to cirrhosis and hepatocellular carcinoma (HCC). The epigenetic events involved in hepatocyte transformation towards malignancy in this context are poorly known. Here we report that, in Huh-7 cells, HDV induces DNMT3b expression and is associated to E2F1 transcription factor hypermethylation. Moreover our cell cycle analysis showed that HDV induces G2/M arrest. These findings suggest that HDV could play a role in HCC development at least in part by altering DNA methylation events. A better understanding of the molecular mechanisms involved in HDV-related carcinogenesis could help to identify new therapeutic targets.
乙型肝炎病毒/δ 型肝炎病毒(HBV/HDV)共感染导致的肝损伤比单纯乙型肝炎病毒感染更为严重,且更容易进展为肝硬化和肝细胞癌(HCC)。然而,在这种情况下,涉及肝细胞向恶性转化的表观遗传事件知之甚少。本研究报告称,HDV 在 Huh-7 细胞中诱导 DNMT3b 表达,并与 E2F1 转录因子的过度甲基化有关。此外,我们的细胞周期分析表明,HDV 诱导 G2/M 期阻滞。这些发现表明,HDV 通过改变 DNA 甲基化事件可能在 HCC 发展中起作用。深入了解与 HDV 相关致癌作用相关的分子机制,有助于识别新的治疗靶点。