大型HBV表面蛋白诱导的未折叠蛋白反应动态调节肝细胞癌进展中的p27降解
Yixiao Guo1, Jie Shao1, Renyu Zhang1
1National Translational Science Center for Molecular Medicine and Department of Cell Biology, Fourth Military Medical University, Xi'an 710032, China.
International journal of molecular sciences
|September 28, 2023
概括
乙型肝炎病毒大表面抗原 (LHB) 驱动肝细胞癌 (HCC) 通过引起细胞内网膜应激,从而破坏细胞循环调节通过p27. 这导致无法控制的细胞生长和与HBV相关的HCC中的瘤进展.
科学领域:
- 肝病学 肝病学是一种肝病学.
- 分子生物学分子生物学
- 在瘤学瘤学.
背景情况:
- 肝细胞癌 (HCC) 经常与乙型肝炎病毒 (HBV) 感染有关.
- 大型HBV表面抗原 (LHB) 与HBV相关的HCC发展和进展有关.
研究的目的:
- 调查LHB在与HBV相关的HCC进展中的作用.
- 阐明LHB,内质网膜 (ER) 应激和HCC中细胞循环调节之间的分子机制.
主要方法:
- 基因组丰富分析以确定LHB调节的途径.
- 在体外和体内研究,以评估LHB对ER应激和细胞周期的影响.
- 对p27调节的分析,包括转录上调和翻译后修改.
主要成果:
- 在HCC细胞中LHB过度表达会诱导慢性ER压力,与瘤生长相关.
- LHB增强了细胞周期从G1到S阶段的进展.
- ER压力通过ATF4和XBP1s提高p27转录的调节,但也通过增强的翻译和无处不在促进p27降解,最终降低p27水平.
结论:
- 由LHB引起的ER压力和随后的p27失调促进细胞循环的进展,有助于HCC的发展.
- 针对ER压力-p27轴可能为HBV相关的HCC提供治疗策略.
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