通过通过NF-κB信号通路调节CCL20,TH1L参与结直肠癌的发病
Shaochang Wang1, Yujing Sun2, Chunya Li1
1The Key Laboratory of Cell Proliferation and Regulation Biology, Ministry of Education, College of Life Sciences, Beijing Normal University, Beijing, China.
Journal of cellular and molecular medicine
|May 29, 2024
概括
转录调节因子TH1L在结直肠癌 (CRC) 中高度表达,并通过CCL20/NF-κB通路促进CRC细胞的增殖和迁移,表明其作为诊断和治疗点的潜力.
科学领域:
- 分子生物学分子生物学
- 癌症研究 癌症研究
- 遗传学 是一个遗传学.
背景情况:
- 作为负延长因子 (NELF) 综合体的一部分,TH1L调节RNA聚合酶II (RNAPII) 转录.
- TH1L在癌症进展中的作用在很大程度上仍然未被描述.
研究的目的:
- 研究TH1L在结直肠癌 (CRC) 中的功能和分子机制.
- 探索TH1L作为CRC的潜在诊断和治疗点.
主要方法:
- 在CRC组织和患者便中分析TH1L表达.
- 细胞增殖和迁移对TH1L过度表达和淘汰的测定.
- RNA测序以确定下游的分子途径.
- 评估NF-κB信号通路的激活情况.
- CCL20 撞击式救援试验.
主要成果:
- 在CRC组织和便中,TH1L表达升高.
- 过度表达TH1L增强了CRC细胞的增殖和迁移.
- 在TH1L上调节CCL20,激活NF-κB通路.
- 抑制CCL20减轻TH1L的促进瘤的作用.
结论:
- TH1L通过CCL20/NF-κB信号通路促进CRC的扩散和迁移.
- TH1L代表了CRC诊断的潜在生物标志物和治疗点.
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