在癌症中,TGF-β和细胞粘附信号通路之间的交叉对话
Jiahao Liao1,2, Rentang Chen1,2, Bihua Lin1
1Guangdong Provincial Key Laboratory of Medical Molecular Diagnostics, Dongguan Key Laboratory of Medical Bioactive Molecular Developmental and Translational Research, The First Dongguan Affiliated Hospital, Guangdong Medical University, Dongguan, Guangdong, 523808, China.
International journal of medical sciences
|May 31, 2024
概括
转化生长因子-β (TGF-β) 信号与细胞粘附分子相互作用,影响细胞行为. 异常的TGF-β激活促进癌症的入侵和转移通过上皮细胞-介质细胞过渡 (EMT).
科学领域:
- 在瘤学瘤学.
- 细胞生物学 细胞生物学
- 分子生物学分子生物学
背景情况:
- 转化生长因子-β (TGF-β) 对于细胞分化和迁移至关重要,与细胞粘附信号通路相互作用.
- TGF-β在一个不活跃的复合体中分泌,需要释放成熟的TGF-β来激活信号通路.
- 细胞粘附分子 (CAMs),特别是整合素,在识别和激活潜伏的TGF-β方面发挥着关键作用.
研究的目的:
- 要总结TGF-β和癌症中的细胞粘附信号之间的交叉声.
- 阐明这种相互作用的潜在分子机制.
主要方法:
- 文献综述和对TGF-β信号传递和癌症细胞粘附现有研究的综合.
- 分析涉及整体,CAMs表达和Smad蛋白,转录因子和非编码RNAs等调节分子的分子机制.
主要成果:
- TGF-β通过调节CAMs的表达来调节细胞粘附.
- 集成蛋白对于成熟的TGF-β的释放和激活至关重要.
- 由失调分子驱动的异常TGF-β通路激活,通过表皮细胞-介质细胞过渡 (EMT) 促进瘤入侵和转移.
结论:
- TGF-β与细胞粘附信号之间的相互作用是癌症进展的关键决定因素.
- 了解这些分子机制为抑制瘤入侵和转移提供了对潜在治疗点的见解.
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