激活HOXC8的TRIM22/NF-κB通路促进结直肠癌的干性
Song Tan1, Yifan Chen1, Yizhen Chen2
1Department of Gastrointestinal Surgery, Shengli Clinical Medical College of Fujian Medical University, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Hospital, No.134, Dongjie, Fuzhou, 350001, China; Shengli Clinical Medical College of Fujian Medical University, Fuzhou, 350013, China.
Cancer letters
|November 20, 2025
概括
过度表达HOXC8可促进结直肠癌 (CRC) 的生长,干性和化学抵抗. 它激活TRIM22,降解IκBα并增强NF-κB信号传递,推动CRC的进展.
科学领域:
- 在瘤学瘤学.
- 分子生物学分子生物学
- 遗传学 是一个遗传学.
背景情况:
- 结肠直肠癌 (CRC) 是全球主要的健康负担,发病率和死亡率高.
- 对于HOXC8家庭盒基因在CRC增殖和干性中的作用尚不清楚.
- 癌症干细胞驱动瘤的开始,转移和治疗抵抗.
研究的目的:
- 研究HOXC8在结直肠癌中的功能作用.
- 阐明HOXC8影响CRC进展和干性的分子机制.
- 为了确定CRC治疗的潜在治疗点.
主要方法:
- 评估了HOXC8过度表达对CRC细胞增殖,干细胞和化学抵抗的影响.
- 调查了HOXC8的下游目标,包括TRIM22.
- 分析了NF-κB信号通路在HOXC8-介导效应中的参与.
主要成果:
- 过度表达HOXC8显著增加了CRC细胞的增殖,干细胞特性和化学抵抗.
- 发现HOXC8可以通过转录激活TRIM22.
- TRIM22调解了IκBα的泛化和降解,导致NF-κB通路的激活和树干维护.
结论:
- HOXC8通过增强扩散,干性和化学抵抗来促进CRC的进展.
- 一个新的信号轴,HOXC8 / TRIM22 / NF-κB,被确定为一个关键的调节器的茎在CRC.
- 准HOXC8/TRIM22/NF-κB通路可能为结直肠癌提供了一个有前途的治疗策略.
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