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WFDC2 通过调节 EGFR 信号失活抑制前列腺癌转移。

WFDC2 suppresses prostate cancer metastasis by modulating EGFR signaling inactivation.

机构信息

Department of Urology, Zhongnan Hospital of Wuhan University, Wuhan, China.

Division of Nephrology, Department of Internal Medicine, Leiden University Medical Center, Leiden, The Netherlands.

出版信息

Cell Death Dis. 2020 Jul 16;11(7):537. doi: 10.1038/s41419-020-02752-y.

Abstract

WAP four-disulfide core domain 2 (WFDC2) is a small secretory protein that has been widely studied in ovarian cancer. It has been proven that WFDC2 promotes proliferation and metastasis in ovarian cancer, and serves as a diagnostic biomarker. However, the specific function of WFDC2 in prostate cancer has not been reported. Here, we first screened the diagnostic marker and favorable prognostic factor WFDC2 in prostate cancer by bioinformatics. WFDC2 expression was negatively correlated with Gleason score and metastasis in prostate cancer. Then, we revealed that overexpression of WFDC2, and addition of recombinant protein HE4 can significantly inhibit prostate cancer metastasis in vivo and in vitro. By co-immunoprecipitation and co-localization assays, we proved that WFDC2 binds to the extracellular domain of epidermal growth factor receptor (EGFR). Immunoblot showed that WFDC2 overexpression and recombinant protein HE4 addition inactivated the EGFR/AKT/GSK3B/Snail signaling pathway, and then restrained the progression of epithelial-mesenchymal transition. In conclusion, our study identified that the tumor suppressor WFDC2 can suppress prostate cancer metastasis by inactivating EGFR signaling.

摘要

WAP 四硫键核心结构域 2(WFDC2)是一种小型分泌蛋白,在卵巢癌中已得到广泛研究。已有研究证实 WFDC2 可促进卵巢癌细胞的增殖和转移,是一种诊断性生物标志物。然而,WFDC2 在前列腺癌中的具体功能尚未有报道。在此,我们首次通过生物信息学筛选出前列腺癌的诊断标志物和有利预后因子 WFDC2。WFDC2 的表达与前列腺癌的 Gleason 评分和转移呈负相关。接着,我们揭示了过表达 WFDC2 和添加重组蛋白 HE4 可显著抑制前列腺癌在体内和体外的转移。通过共免疫沉淀和共定位实验,我们证明 WFDC2 与表皮生长因子受体(EGFR)的细胞外结构域结合。免疫印迹显示,过表达 WFDC2 和添加重组蛋白 HE4 可使 EGFR/AKT/GSK3B/Snail 信号通路失活,从而抑制上皮-间充质转化的进展。综上所述,我们的研究表明肿瘤抑制因子 WFDC2 可通过使 EGFR 信号失活来抑制前列腺癌的转移。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bee/7366654/767287e2188f/41419_2020_2752_Fig1_HTML.jpg

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