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全反式视黄醇结合蛋白及其受体STRA6驱动致癌转化。

Holo-retinol-binding protein and its receptor STRA6 drive oncogenic transformation.

作者信息

Berry Daniel C, Levi Liraz, Noy Noa

机构信息

Department of Cellular & Molecular Medicine, Lerner Research Institute, Cleveland Clinic, and Departments of Pharmacology and Nutrition, Case Western Reserve University School of Medicine, Cleveland, Ohio.

出版信息

Cancer Res. 2014 Nov 1;74(21):6341-51. doi: 10.1158/0008-5472.CAN-14-1052. Epub 2014 Sep 18.

Abstract

Vitamin A, retinol, circulates in blood bound to retinol-binding protein (RBP). At some tissues, RBP is recognized by STRA6, a plasma membrane protein that serves a dual role: it transports retinol from extracellular RBP into cells and it transduces a signaling cascade mediated by the Janus kinase JAK2 and the transcription factors STAT3 and STAT5. We show here that expression of RBP and STRA6 is markedly upregulated in human breast and colon tumors, that holo-RBP/STRA6 signaling promotes oncogenic properties, and that STRA6 expression is critical for tumor formation by colon carcinoma cells in vivo. The holo-RBP/STRA6 pathway also efficiently induces fibroblasts to undergo oncogenic transformation, rendering them highly tumorigenic. These data establish that holo-RBP and its receptor STRA6 are potent oncogenes and suggest that the pathway is a novel target for therapy of some human cancers.

摘要

维生素A,即视黄醇,在血液中与视黄醇结合蛋白(RBP)结合循环。在某些组织中,STRA6可识别RBP,STRA6是一种质膜蛋白,具有双重作用:它将视黄醇从细胞外的RBP转运到细胞内,并转导由Janus激酶JAK2以及转录因子STAT3和STAT5介导的信号级联反应。我们在此表明,RBP和STRA6的表达在人类乳腺和结肠肿瘤中显著上调,全反式视黄醇结合蛋白/STRA6信号传导促进致癌特性,并且STRA6表达对于体内结肠癌细胞形成肿瘤至关重要。全反式视黄醇结合蛋白/STRA6途径还能有效诱导成纤维细胞发生致癌转化,使其具有高度致瘤性。这些数据证实全反式视黄醇结合蛋白及其受体STRA6是强效致癌基因,并表明该途径是某些人类癌症治疗的新靶点。

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