Definition of PKC-α, CDK6, and MET as Therapeutic Targets in Triple-Negative Breast Cancer

被引:58
|
作者
Hsu, Yi-Hsin [1 ]
Yao, Jun [1 ]
Chan, Li-Chuan [1 ,2 ]
Wu, Ting-Jung [1 ,3 ]
Hsu, Jennifer L. [1 ,4 ,5 ,6 ]
Fang, Yueh-Fu [1 ,7 ]
Wei, Yongkun [1 ]
Wu, Yun [8 ]
Huang, Wen-Chien [9 ]
Liu, Chien-Liang [9 ]
Chang, Yuan-Ching [9 ]
Wang, Ming-Yang [1 ,10 ]
Li, Chia-Wei [1 ]
Shen, Jia [1 ,2 ]
Chen, Mei-Kuang [2 ]
Sahin, Aysegul A. [8 ]
Sood, Anil [2 ,11 ]
Mills, Gordon B. [2 ,12 ]
Yu, Dihua [1 ,2 ]
Hortobagyi, Gabriel N. [13 ]
Hung, Mien-Chie [1 ,2 ,4 ,5 ,6 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Mol & Cellular Oncol, Houston, TX 77030 USA
[2] Univ Texas, Grad Sch Biomed Sci Houston, Houston, TX USA
[3] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp Linkou, Dept Gen Surg, Taipei, Taiwan
[4] China Med Univ, Grad Inst Canc Biol, Taichung, Taiwan
[5] China Med Univ, Ctr Mol Med, Taichung, Taiwan
[6] Asia Univ, Dept Biotechnol, Taichung, Taiwan
[7] Chang Gung Univ, Coll Med, Chang Gung Mem Hosp Linkou, Dept Internal Med, Taipei, Taiwan
[8] Univ Texas MD Anderson Canc Ctr, Dept Pathol, Houston, TX 77030 USA
[9] Mackay Mem Hosp, Mackay Jr Coll Med Nursing & Management, Dept Surg, Taipei, Taiwan
[10] Natl Taiwan Univ Hosp, Dept Surg, Taipei 100, Taiwan
[11] Univ Texas MD Anderson Canc Ctr, Dept Gynecol Oncol & Reprod Med, Houston, TX 77030 USA
[12] Univ Texas MD Anderson Canc Ctr, Dept Syst Biol, Houston, TX 77030 USA
[13] Univ Texas MD Anderson Canc Ctr, Dept Breast Med Oncol, Houston, TX 77030 USA
关键词
PROTEIN-KINASE; INHIBITOR OLAPARIB; ANALYSIS TOOL; STEM-CELLS; PHASE-I; COMBINATION; EXPRESSION; SURVIVAL; TRIAL; IDENTIFICATION;
D O I
10.1158/0008-5472.CAN-14-0584
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
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-alpha. MET, and CHK6 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 turnorigenic potential in a cooperative manner. A combination of PKC-alpha-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. (C)2014 AACR
引用
收藏
页码:4822 / 4835
页数:14
相关论文
共 50 条
  • [31] CDK4 regulates cancer stemness and is a novel therapeutic target for triple-negative breast cancer
    Meiou Dai
    Chenjing Zhang
    Ayad Ali
    Xinyuan Hong
    Jun Tian
    Chieh Lo
    Nadège Fils-Aimé
    Sergio A. Burgos
    Suhad Ali
    Jean-Jacques Lebrun
    Scientific Reports, 6
  • [32] CDK4 regulates cancer stemness and is a novel therapeutic target for triple-negative breast cancer
    Dai, Meiou
    Zhang, Chenjing
    Ali, Ayad
    Hong, Xinyuan
    Tian, Jun
    Lo, Chieh
    Fils-Aime, Nadege
    Burgos, Sergio A.
    Ali, Suhad
    Lebrun, Jean-Jacques
    SCIENTIFIC REPORTS, 2016, 6
  • [33] Histone Deacetylases as New Therapeutic Targets in Triple-negative Breast Cancer: Progress and Promises
    Garmpis, Nikolaos
    Damaskos, Christos
    Garmpi, Anna
    Kalampokas, Emmanouil
    Kalampokas, Theodoros
    Spartalis, Eleftherios
    Daskalopoulou, Afrodite
    Valsami, Serena
    Kontos, Michael
    Nonni, Afroditi
    Kontzoglou, Konstantinos
    Perrea, Despina
    Nikiteas, Nikolaos
    Dimitroulis, Dimitrios
    CANCER GENOMICS & PROTEOMICS, 2017, 14 (05) : 299 - 313
  • [34] Potential therapeutic targets of triple-negative breast cancer based on its intrinsic subtype
    Shao, Fangyuan
    Sun, Heng
    Deng, Chu-Xia
    ONCOTARGET, 2017, 8 (42) : 73329 - 73344
  • [35] Narrowing the focus: Therapeutic cell surface targets for refractory triple-negative breast cancer
    Tafreshi, Narges K.
    Morse, David L.
    Lee, Marie Catherine
    WORLD JOURNAL OF CLINICAL ONCOLOGY, 2020, 11 (04):
  • [36] Functional pathways analyses to identify candidate therapeutic targets in triple-negative breast cancer
    Andre, F.
    Dessen, P.
    Job, B.
    Delaloge, S.
    Pusztai, L.
    Lazar, V.
    JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (15)
  • [37] Triple-negative breast cancer: from none to multiple therapeutic targets in two decades
    Carvalho, Filomena Marino
    FRONTIERS IN ONCOLOGY, 2023, 13
  • [38] Targeted Therapeutic Strategies for Triple-Negative Breast Cancer
    Li, Ying
    Zhan, Zhijun
    Yin, Xuemin
    Fu, Shujun
    Deng, Xiyun
    FRONTIERS IN ONCOLOGY, 2021, 11
  • [39] Potential therapeutic target for triple-negative breast cancer
    Gilbert, Judith A.
    LANCET ONCOLOGY, 2012, 13 (08): : E330 - E330
  • [40] New Therapeutic Strategies for Triple-Negative Breast Cancer
    Szekely, Borbala
    Silber, Andrea L. M.
    Pusztai, Lajos
    ONCOLOGY-NEW YORK, 2017, 31 : 13 - 20