素通过调节O-GlcNAcylation来抑制肝细胞癌
Xiang Zhang1, Li-Qiong Wang2, Zhi-Yong Liu3
1Department of Traditional Chinese Medicine, Qingpu Branch of Zhongshan Hospital Affiliated to Fudan University, Shanghai 201700, China.
World journal of gastrointestinal oncology
|October 1, 2024
概括
素减少O-GlcNAcylation和OGT表达,通过影响NF-κB和JNK通路来抑制肝细胞癌 (HCC) 的生长和转移.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 生物化学 生物化学
背景情况:
- 肝细胞癌 (HCC) 的发病过程复杂,机制不清楚.
- 许多风险因素有助于HCC的发展.
研究的目的:
- 为了调查塞内基宁和O-GlcNAcylation在HCC生长和转移中的作用.
- 阐明在HCC中受到senegenin和O-GlcNAcylation影响的分子通路.
主要方法:
- 西部斑点分析检测HCC组织和细胞中的O-链接的N-乙糖胺转移酶 (OGT) 和O-GlcNAcylation水平.
- 在体外测试 (细胞计数套件-8,克隆原性,跨井迁移) 以评估原素和O-GlcNAcylation对HCC细胞增殖和转移的影响.
- 通过药物治疗和病毒感染操纵O-GlcNAcylation水平,然后对通路蛋白进行西部斑分析.
主要成果:
- 在HCC组织和细胞中,OGT和O-GlcNAcylation水平显著升高.
- 增加的O-GlcNAcylation与增强的增殖,侵入性,克隆性和转移潜力相关.
- 素治疗降低了O-GlcNAcylation,减缓了HCC细胞的增殖和迁移.
- 观察到核因子-kappa B (NF-κB) 和c-Jun N-终端激酶 (JNK) 途径中的蛋白质水平发生变化.
结论:
- 素有效降低了HCC中的O-GlcNAcylation和OGT表达.
- 素通过调节NF-κB和JNK通路来抑制HCC细胞生长和转移.
- 这项研究强调了塞内基宁作为一种潜在的治疗剂,针对HCC中的O-GlcNAcylation.
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