Literature DB >> 21243019

Blockade of testicular and adrenal androgens in prostate cancer treatment.

Fernand Labrie1.   

Abstract

Prostate cancer is the most hormone sensitive of all cancers. However, any hormonal therapeutic strategy must take into account the fact that two almost equivalent sources of androgens act in the prostate, namely testosterone of testicular origin, and the locally produced androgens testosterone and dihydrotestosterone (DHT) derived from dehydroepiandrosterone of adrenal origin. Combined androgen blockade--medical or surgical castration plus a pure antiandrogen--would, therefore, be the logical first-line treatment for prostate cancer, although castration or an antiandrogen alone is still chosen in the majority of cases. Although long-term control, or even cure, is possible when combined androgen blockade is used when the tumor is localized, resistance to treatment invariably develops in patients when start of treatment is delayed until the disease has become metastatic. This observation can be explained either by elevated levels of the androgen receptor, which can increase the response to low levels of androgens and also modify the response to antiandrogens; or by local biosynthesis of androgens. Research to identify new and more potent antiandrogens, as well as blockers of peripheral and adrenal androgen biosynthesis--such as abiraterone--could be of great importance.

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Year:  2011        PMID: 21243019     DOI: 10.1038/nrurol.2010.231

Source DB:  PubMed          Journal:  Nat Rev Urol        ISSN: 1759-4812            Impact factor:   14.432


  85 in total

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5.  Increased expression of genes converting adrenal androgens to testosterone in androgen-independent prostate cancer.

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6.  Molecular determinants of resistance to antiandrogen therapy.

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7.  Mutant androgen receptor detected in an advanced-stage prostatic carcinoma is activated by adrenal androgens and progesterone.

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9.  A wide range of sensitivities to androgens develops in cloned Shionogi mouse mammary tumor cells.

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Journal:  Endocrinology       Date:  1989-06       Impact factor: 4.736

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Review 7.  New Opportunities for Targeting the Androgen Receptor in Prostate Cancer.

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8.  Implications of pleiotrophin in human PC3 prostate cancer cell growth in vivo.

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9.  PSA screening for prostate cancer: why so much controversy?

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10.  SGK3 is an androgen-inducible kinase promoting prostate cancer cell proliferation through activation of p70 S6 kinase and up-regulation of cyclin D1.

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