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纤连蛋白通过 CDC42-YAP 依赖性信号通路促进结直肠癌细胞的生长和耐药性。

Fibronectin promotes tumor cells growth and drugs resistance through a CDC42-YAP-dependent signaling pathway in colorectal cancer.

机构信息

Department of General Surgery, Zhejiang Chinese Medicine and Western Medicine Integrated Hospital/Hangzhou Red Cross Hospital, Hangzhou, China.

Department of Gastrointestinal Surgery, Shanxian Dongda Hospital, Heze, China.

出版信息

Cell Biol Int. 2020 Sep;44(9):1840-1849. doi: 10.1002/cbin.11390. Epub 2020 Jun 8.

Abstract

Fibronectin (FN) is a high-molecular-weight glycoprotein of the extracellular matrix (ECM) that binds to membrane-spanning receptor proteins or other elements in ECM. The expression of FN could be involved in the cancer cells proliferation or migration, and the molecular mechanisms responsible for FN induced protumor signals begin to be elucidated. Here, we report that the elevated expression of FN was observed in those chemoresistant tumor tissues from patients with colorectal cancer. Consistently, FN culture significantly strengthened the proliferation of colorectal cancer cells, induced the colorectal tumor sustained growth and drug resistance in vitro and in vivo. In mechanism, FN could bind to integrin αvβ1, resulting the downstream cell division cycle 42/yes-associated protein 1 (CDC42/YAP-1) signaling pathway activation. The activation of CDC42/YAP-1 signal induces the upregulation of transcription factor SOX2, causing the sustained growth and drugs resistance in colorectal cancer. Blockade of integrin αvβ1 significantly suppressed the colorectal cancer growth and drugs resistance development in vitro and in vivo, which provides a new target for clinical colorectal cancer treatment.

摘要

纤连蛋白(FN)是细胞外基质(ECM)中的一种高分子量糖蛋白,它与跨膜受体蛋白或 ECM 中的其他元件结合。FN 的表达可能参与癌细胞的增殖或迁移,并且负责 FN 诱导的促肿瘤信号的分子机制开始被阐明。在这里,我们报告在患有结直肠癌的患者的耐药性肿瘤组织中观察到 FN 的表达升高。一致地,FN 培养显著增强了结直肠癌细胞的增殖,在体外和体内诱导结直肠肿瘤持续生长和耐药性。在机制上,FN 可以与整合素 αvβ1 结合,导致下游细胞分裂周期 42/yes 相关蛋白 1(CDC42/YAP-1)信号通路的激活。CDC42/YAP-1 信号的激活诱导转录因子 SOX2 的上调,导致结直肠癌细胞的持续生长和耐药性。阻断整合素 αvβ1 可显著抑制结直肠癌细胞在体外和体内的生长和耐药性发展,为结直肠癌的临床治疗提供了新的靶点。

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