Targeting molecular resistance in castration-resistant prostate cancer

被引:47
作者
Chandrasekar, Thenappan [1 ]
Yang, Joy C. [1 ]
Gao, Allen C. [1 ]
Evans, Christopher P. [1 ]
机构
[1] Univ Calif Davis, Dept Urol, Davis, CA 95616 USA
来源
BMC MEDICINE | 2015年 / 13卷
关键词
Castration-resistant; Disease progression; Drug resistance; Prostatic neoplasms; ANDROGEN RECEPTOR GENE; OVERCOMES ENZALUTAMIDE RESISTANCE; III BETA-TUBULIN; SPLICE VARIANT; ABIRATERONE ACETATE; CYP17A1; INHIBITION; INCREASED SURVIVAL; CLINICAL ACTIVITY; PLUS PREDNISONE; CELL BIOLOGY;
D O I
10.1186/s12916-015-0457-6
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple mechanisms of resistance contribute to the inevitable progression of hormone-sensitive prostate cancer to castration-resistant prostate cancer (CRPC). Currently approved therapies for CRPC include systemic chemotherapy (docetaxel and cabazitaxel) and agents targeting the resistance pathways leading to CRPC, including enzalutamide and abiraterone. While there is significant survival benefit, primary and secondary resistance to these therapies develops rapidly. Up to one-third of patients have primary resistance to enzalutamide and abiraterone; the remaining patients eventually progress on treatment. Understanding the mechanisms of resistance resulting in progression as well as identifying new targetable pathways remains the focus of current prostate cancer research. We review current knowledge of mechanisms of resistance to the currently approved treatments, development of adjunctive therapies, and identification of new pathways being targeted for therapeutic purposes.
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页数:10
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共 115 条
  • [111] Novel Membrane-associated Androgen Receptor Splice Variant Potentiates Proliferative and Survival Responses in Prostate Cancer Cells
    Yang, Xi
    Guo, Zhiyong
    Sun, Feng
    Li, Wei
    Alfano, Alan
    Shimelis, Hermela
    Chen, Mingyuan
    Brodie, Angela M. H.
    Chen, Hegang
    Xiao, Zhen
    Veenstra, Timothy D.
    Qiu, Yun
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2011, 286 (41) : 36152 - 36160
  • [112] Steroidogenic Enzyme AKR1C3 Is a Novel Androgen Receptor-Selective Coactivator that Promotes Prostate Cancer Growth
    Yepuru, Muralimohan
    Wu, Zhongzhi
    Kulkarni, Anand
    Yin, Feng
    Barrett, Christina M.
    Kim, Juhyun
    Steiner, Mitchell S.
    Miller, Duane D.
    Dalton, James T.
    Narayanan, Ramesh
    [J]. CLINICAL CANCER RESEARCH, 2013, 19 (20) : 5613 - 5625
  • [113] Clusterin inhibits apoptosis by interacting with activated Bax
    Zhang, HL
    Kim, JK
    Edwards, CA
    Xu, ZH
    Taichman, R
    Wang, CY
    [J]. NATURE CELL BIOLOGY, 2005, 7 (09) : 909 - U69
  • [114] Induction of Clusterin by AKT-Role in Cytoprotection against Docetaxel in Prostate Tumor Cells
    Zhong, Bin
    Sallman, David A.
    Gilvary, Danielle L.
    Pernazza, Daniele
    Sahakian, Eva
    Fritz, Dillon
    Cheng, Jin Q.
    Trougakos, Ioannis
    Wei, Sheng
    Djeu, Julie Y.
    [J]. MOLECULAR CANCER THERAPEUTICS, 2010, 9 (06) : 1831 - 1841
  • [115] Inhibition of ABCB1 Expression Overcomes Acquired Docetaxel Resistance in Prostate Cancer
    Zhu, Yezi
    Liu, Chengfei
    Nadiminty, Nagalakshmi
    Lou, Wei
    Tummala, Ramakumar
    Evans, Christopher P.
    Gao, Allen C.
    [J]. MOLECULAR CANCER THERAPEUTICS, 2013, 12 (09) : 1829 - 1836