Transition to androgen-independence in prostate cancer

被引:81
作者
Navarro, D
Luzardo, OP
Fernández, L
Chesa, N
Díaz-Chico, BN
机构
[1] ICIC, Dept Biochem, Las Palmas Gran Canaria 35080, Canary Islands, Spain
[2] ICIC, Dept Physiol, Las Palmas Gran Canaria 35080, Canary Islands, Spain
[3] ICIC, Dept Clin Sci, Las Palmas Gran Canaria 35080, Canary Islands, Spain
[4] Univ Las Palmas Gran Canaria, Hosp Insular Gran Canaria, ICIC, Serv Urol,Dept Med Sci, Las Palmas Gran Canaria 35080, Canary Islands, Spain
[5] Univ Las Palmas Gran Canaria, Hosp Insular Gran Canaria, ICIC, Serv Urol,Dept Chirurg Sci, Las Palmas Gran Canaria 35080, Canary Islands, Spain
关键词
transition; androgen-independence; prostate cancer;
D O I
10.1016/S0960-0760(02)00064-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prostate carcinoma is the most frequently diagnosed malignancy and the second leading cause of death as a result of cancer in men in the western countries. Withdrawal of androgens or the peripheral blockage of androgen action remain the critical therapeutic options for the treatment of advanced prostate cancer. However. after initial regression, most of the prostate cancers become androgen-independent and progress further with eventual fatal outcome. Understanding the mechanisms of transition to androgen independence and tumor progression in prostate cancer is critical to finding new ways to treat aged patients that are ineligible for conventional chemotherapy. A large number of different molecular mechanisms might be responsible for the transition to androgen-independence. Many of these involve the androgen receptor (AR) and its signalling pathways. but they might also include genetic chances that affect several genes, which results in the activation of oncogenes or the inactivation of tumor suppressor genes. Here. we discuss the Most recent and relevant findings on androgen resistance in prostate cancer in order provide a comprehensive interpretation of the clinical behaviour of tumors at molecular levels. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:191 / 201
页数:11
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