ROR1 Is Expressed in Human Breast Cancer and Associated with Enhanced Tumor-Cell Growth

Suping Zhang(University of California, San Diego), Liguang Chen(University of California, San Diego), Bing Cui(University of California, San Diego), Han‐Yu Chuang(University of California, San Diego), Jianqiang Yu(University of California, San Diego), Jessica Wang‐Rodriguez(University of California, San Diego), Tang Li(University of California, San Diego), George Chen(University of California, San Diego), Grzegorz Basak(University of California, San Diego), Thomas J. Kipps(University of California, San Diego)
PLoS ONE
March 5, 2012
Cited by 260Open Access
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Abstract

Receptor-tyrosine-kinase-like orphan receptor 1 (ROR1) is expressed during embryogenesis and by certain leukemias, but not by normal adult tissues. Here we show that the neoplastic cells of many human breast cancers express the ROR1 protein and high-level expression of ROR1 in breast adenocarcinoma was associated with aggressive disease. Silencing expression of ROR1 in human breast cancer cell lines found to express this protein impaired their growth in vitro and also in immune-deficient mice. We found that ROR1 could interact with casein kinase 1 epsilon (CK1ε) to activate phosphoinositide 3-kinase-mediated AKT phosphorylation and cAMP-response-element-binding protein (CREB), which was associated with enhanced tumor-cell growth. Wnt5a, a ligand of ROR1, could induce ROR1-dependent signaling and enhance cell growth. This study demonstrates that ROR1 is expressed in human breast cancers and has biological and clinical significance, indicating that it may be a potential target for breast cancer therapy.


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