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缺氧诱导的Wnt5a分泌纤维细胞促进结肠癌的进展
Akikazu Harada1,2,3, Yoshiaki Yasumizu4,5, Takeshi Harada6
1Center for Infectious Disease Education and Research (CiDER), The University of Osaka, Suita, Osaka, Japan. aharada@cider.osaka-u.ac.jp.
Nature communications
|April 17, 2025
概括
由炎症性纤维细胞产生的Wnt5a蛋白通过创造低氧瘤微环境来推动结肠癌的生长. 削减Wnt5a抑制了瘤的形成,提供了一个潜在的治疗点.
科学领域:
- 在瘤学瘤学.
- 细胞生物学 细胞生物学
- 癌症研究 癌症研究
背景情况:
- Wnt5a是一种Wnt连接体,可以激活β-catenin独立路径并促进瘤发生.
- 它的生产地点和对结肠癌攻击性的影响仍然不清楚.
研究的目的:
- 调查结肠癌中Wnt5a生产的来源.
- 阐明Wnt5a影响结肠癌进展的机制.
主要方法:
- 对人类和小鼠结肠纤维细胞单细胞RNA-seq数据的元分析.
- 在体内研究涉及Wnt5a在小鼠模型中的耗尽.
- 纤维细胞-内皮细胞相互作用和分子信号通路的分析.
主要成果:
- Wnt5a在瘤光侧附近的纤维细胞中表达,被确定为低氧诱导的炎症性纤维细胞 (InfFib) 与激活的HIF2.2.
- Wnt5a通过通过内皮细胞的Flt1分泌抑制血管生成来维持InfFib,从而诱导缺氧.
- InfFib产生epiregulin,促进结肠癌的生长.
结论:
- Wnt5a通过诱导低氧微环境来推动结肠癌的进展,从而维持InfFib.
- 向Wnt5a或InfFib可能是结肠癌的新疗法策略.
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