| Literature DB >> 24970481 |
Yi-Hsin Hsu1, Jun Yao1, Li-Chuan Chan2, Ting-Jung Wu3, Jennifer L Hsu4, Yueh-Fu Fang5, Yongkun Wei1, Yun Wu6, Wen-Chien Huang7, Chien-Liang Liu7, Yuan-Ching Chang7, Ming-Yang Wang8, Chia-Wei Li1, Jia Shen2, Mei-Kuang Chen9, Aysegul A Sahin6, Anil Sood10, Gordon B Mills11, Dihua Yu2, Gabriel N Hortobagyi12, Mien-Chie Hung13.
Abstract
Triple-negative breast cancer (TNBC) is a highly heterogeneous and recurrent subtype of breast cancer that lacks an effective targeted therapy. To identify candidate therapeutic targets, we profiled global gene expression in TNBC and breast tumor-initiating cells with a patient survival dataset. Eight TNBC-related kinases were found to be overexpressed in TNBC cells with stem-like properties. Among them, expression of PKC-α, MET, and CDK6 correlated with poorer survival outcomes. In cases coexpressing two of these three kinases, survival rates were lower than in cases where only one of these kinases was expressed. In functional tests, two-drug combinations targeting these three kinases inhibited TNBC cell proliferation and tumorigenic potential in a cooperative manner. A combination of PKC-α-MET inhibitors also attenuated tumor growth in a cooperative manner in vivo. Our findings define three kinases critical for TNBC growth and offer a preclinical rationale for their candidacy as effective therapeutic targets in treating TNBC. ©2014 American Association for Cancer Research.Entities:
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Year: 2014 PMID: 24970481 PMCID: PMC4154991 DOI: 10.1158/0008-5472.CAN-14-0584
Source DB: PubMed Journal: Cancer Res ISSN: 0008-5472 Impact factor: 12.701