Medical Faculty, Kunming University of Science and Technology, Kunming 650500, China.
Institute of Medical Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, Kunming 650038, China.
Acta Biochim Biophys Sin (Shanghai). 2024 Jun 14;56(9):1365-1372. doi: 10.3724/abbs.2024091.
Hepatitis E virus (HEV) is the major pathogen of viral hepatitis. Immunocompromised individuals infected by HEV are prone to chronic hepatitis and increase the risk of hepato-cellular carcinoma (HCC). Inhibitor of growth family member 5 (ING5) is a tumor suppressor that is expressed at low levels in cancer tumors or cells. However, the underlying relationship between ING5 and HEV infection is unclear. In the present study, acute and chronic HEV animal models are used to explore the interaction between ING5 and HEV. Notably, the expression of ING5 is significantly increased in both the livers of acute HEV-infected BALB/c mice and chronic HEV-infected rhesus macaques. In addition, the relationship between HEV infection and ING5 expression is further identified in human hepatoma (HepG-2) cells. In conclusion, HEV infection strongly upregulates ING5 expression both and , which has significant implications for further understanding the pathogenic mechanism of HEV infection.
戊型肝炎病毒(HEV)是病毒性肝炎的主要病原体。免疫功能低下的 HEV 感染者易发生慢性肝炎,并增加肝细胞癌(HCC)的风险。生长抑制因子家族成员 5(ING5)是一种肿瘤抑制因子,在癌症肿瘤或细胞中低表达。然而,ING5 与 HEV 感染之间的潜在关系尚不清楚。在本研究中,使用急性和慢性 HEV 动物模型来探索 ING5 与 HEV 之间的相互作用。值得注意的是,急性 HEV 感染的 BALB/c 小鼠和慢性 HEV 感染的恒河猴肝脏中 ING5 的表达均显著增加。此外,还在人肝癌(HepG-2)细胞中进一步确定了 HEV 感染与 ING5 表达之间的关系。总之,HEV 感染强烈地上调 ING5 的表达,这对进一步了解 HEV 感染的致病机制具有重要意义。