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鉴定 CDCP1 为缺氧诱导因子 2α(HIF-2α)的靶基因,与透明细胞肾细胞癌患者的生存相关。

Identification of CDCP1 as a hypoxia-inducible factor 2α (HIF-2α) target gene that is associated with survival in clear cell renal cell carcinoma patients.

机构信息

Department of Systems Biology, Harvard Medical School, Boston, MA 02115, USA.

出版信息

Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3483-8. doi: 10.1073/pnas.1222435110. Epub 2013 Feb 1.

Abstract

CUB domain-containing protein 1 (CDCP1) is a transmembrane protein that is highly expressed in stem cells and frequently overexpressed and tyrosine-phosphorylated in cancer. CDCP1 promotes cancer cell metastasis. However, the mechanisms that regulate CDCP1 are not well-defined. Here we show that hypoxia induces CDCP1 expression and tyrosine phosphorylation in hypoxia-inducible factor (HIF)-2α-, but not HIF-1α-, dependent fashion. shRNA knockdown of CDCP1 impairs cancer cell migration under hypoxic conditions, whereas overexpression of HIF-2α promotes the growth of tumor xenografts in association with enhanced CDCP1 expression and tyrosine phosphorylation. Immunohistochemistry analysis of tissue microarray samples from tumors of patients with clear cell renal cell carcinoma shows that increased CDCP1 expression correlates with decreased overall survival. Together, these data support a critical role for CDCP1 as a unique HIF-2α target gene involved in the regulation of cancer metastasis, and suggest that CDCP1 is a biomarker and potential therapeutic target for metastatic cancers.

摘要

CUB 结构域包含蛋白 1(CDCP1)是一种跨膜蛋白,在干细胞中高度表达,在癌症中常过表达和酪氨酸磷酸化。CDCP1 促进癌细胞转移。然而,调节 CDCP1 的机制尚不清楚。在这里,我们表明缺氧以依赖于缺氧诱导因子 (HIF)-2α、而非 HIF-1α 的方式诱导 CDCP1 的表达和酪氨酸磷酸化。shRNA 敲低 CDCP1 可损害缺氧条件下的癌细胞迁移,而 HIF-2α 的过表达与增强的 CDCP1 表达和酪氨酸磷酸化一起促进肿瘤异种移植物的生长。来自透明细胞肾细胞癌患者肿瘤的组织微阵列样本的免疫组织化学分析表明,CDCP1 表达增加与总生存期降低相关。总之,这些数据支持 CDCP1 作为参与癌症转移调节的独特 HIF-2α 靶基因的关键作用,并表明 CDCP1 是转移性癌症的生物标志物和潜在治疗靶点。

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