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Definition of PKC-α, CDK6, and MET as therapeutic targets in triple-negative breast cancer

  • Yi Hsin Hsu
  • , Jun Yao
  • , Li Chuan Chan
  • , Ting Jung Wu
  • , Jennifer L. Hsu
  • , Yueh Fu Fang
  • , Yongkun Wei
  • , Yun Wu
  • , Wen Chien Huang
  • , Chien Liang Liu
  • , Yuan Ching Chang
  • , Ming Yang Wang
  • , Chia Wei Li
  • , Jia Shen
  • , Mei Kuang Chen
  • , Aysegul A. Sahin
  • , Anil Sood
  • , Gordon B. Mills
  • , Dihua Yu
  • , Gabriel N. Hortobagyi
  • Mien Chie Hung*
*此作品的通信作者
  • University of Texas MD Anderson Cancer Center
  • University of Texas Health Science Center at Houston
  • Chang Gung University
  • China Medical University Taichung
  • Asia University Taiwan
  • Mackay Medicine, Nursing and Management College Taiwan
  • National Taiwan University

研究成果: 期刊稿件 › 文章 › 同行評審

63 引文 斯高帕斯(Scopus)

摘要

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.

原文英語
頁(從 - 到)4822-4835
頁數14
期刊Cancer Research
卷74
發行號17
DOIs
出版狀態已出版 - 01 09 2014
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Publisher Copyright:
© 2014 American Association for Cancer Research.

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