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Wnt/β-连环蛋白/血管舒张刺激磷蛋白正反馈回路驱动乳腺癌细胞的增殖和迁移。

The Wnt/β-catenin/VASP positive feedback loop drives cell proliferation and migration in breast cancer.

作者信息

Li Kai, Zhang Jingwei, Tian Yihao, He Yanqi, Xu Xiaolong, Pan Wenting, Gao Yang, Chen Fangfang, Wei Lei

机构信息

Department of Pathology and Pathophysiology, Hubei Provincial Key Laboratory of Developmentally Originated Disease, School of Basic Medical Sciences, Wuhan University, 185 Donghu Road, Wuchang District, Wuhan, 430071, Hubei, China.

Henan Key Laboratory of Zhang Zhongjing Formulae and Herbs for Immunoregulation, Zhang Zhongjing College of Chinese Medicine, Nanyang Institute of Technology, Nanyang, 473004, Henan, China.

出版信息

Oncogene. 2020 Mar;39(11):2258-2274. doi: 10.1038/s41388-019-1145-3. Epub 2019 Dec 12.

Abstract

Previous studies have shown that the main function of VASP is to regulate the cytoskeleton and play an important role in promoting tumor cell metastasis. In this study, we first reveal that VASP is located in the nucleus of breast cancer cells and elucidate a Wnt/β-catenin/VASP positive feedback loop. We identify that VASP is a target gene of Wnt/β-catenin signaling pathway, and activation of Wnt/β-catenin signaling pathway can significantly upregulate VASP protein expression, while upregulated VASP protein can in turn promote translocation of β-catenin and DVL3 proteins into the nucleus. In the nucleus, VASP, DVL3, β-catenin, and TCF4 can form VASP/DVL3/β-catenin/TCF4 protein complex, activating Wnt/β-catenin signaling pathway, and promoting the expression of target genes VASP, c-myc, and cyclin D1. Thus, our study reveals that there is a Wnt/β-catenin/VASP malignant positive feedback loop in breast cancer, which promotes the proliferation and migration of breast cancer cells, and breaking this positive feedback loop may provide new strategy for breast cancer treatment.

摘要

先前的研究表明,VASP的主要功能是调节细胞骨架,并在促进肿瘤细胞转移中发挥重要作用。在本研究中,我们首次揭示VASP定位于乳腺癌细胞核中,并阐明了一个Wnt/β-连环蛋白/VASP正反馈环。我们确定VASP是Wnt/β-连环蛋白信号通路的一个靶基因,Wnt/β-连环蛋白信号通路的激活可显著上调VASP蛋白表达,而上调的VASP蛋白反过来又可促进β-连环蛋白和DVL3蛋白向细胞核的转运。在细胞核中,VASP、DVL3、β-连环蛋白和TCF4可形成VASP/DVL3/β-连环蛋白/TCF4蛋白复合物,激活Wnt/β-连环蛋白信号通路,并促进靶基因VASP、c-myc和细胞周期蛋白D1的表达。因此,我们的研究揭示了乳腺癌中存在一个Wnt/β-连环蛋白/VASP恶性正反馈环,其促进乳腺癌细胞的增殖和迁移,打破这个正反馈环可能为乳腺癌治疗提供新策略。

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