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Transcriptional network of androgen receptor in prostate cancer progression.

Abstract
The androgen receptor belongs to the nuclear receptor superfamily and functions as a ligand-dependent transcription factor. It binds to the androgen responsive element and recruits coregulatory factors to modulate gene transcription. In addition, the androgen receptor interacts with other transcription factors, such as forkhead box A1, and other oncogenic signaling pathway molecules that bind deoxyribonucleic acid and regulate transcription. Androgen receptor signaling plays an important role in the development of prostate cancer. Prostate cancer cells proliferate in an androgen-dependent manner, and androgen receptor blockade is effective in prostate cancer therapy. However, patients often progress to castration-resistant prostate cancer with elevated androgen receptor expression and hypersensitivity to androgen. Recently, comprehensive analysis tools, such as complementary DNA microarray, chromatin immunoprecipitation-on-chip and chromatin immunoprecipitation-sequence, have described the androgen-mediated diverse transcriptional program and gene networks in prostate cancer. Furthermore, functional and clinical studies have shown that some of the androgen receptor-regulated genes could be prognostic markers and potential therapeutic targets for the treatment of prostate cancer, particularly castration-resistant prostate cancer. Thus, identifying androgen receptor downstream signaling events and investigating the regulation of androgen receptor activity is critical for understanding the mechanism of carcinogenesis and progression to castration-resistant prostate cancer.
AuthorsKen-ichi Takayama, Satoshi Inoue
JournalInternational journal of urology : official journal of the Japanese Urological Association (Int J Urol) Vol. 20 Issue 8 Pg. 756-68 (Aug 2013) ISSN: 1442-2042 [Electronic] Australia
PMID23600948 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
Copyright© 2013 The Japanese Urological Association.
Chemical References
  • Receptors, Androgen
Topics
  • Disease Progression
  • Gene Expression Regulation, Neoplastic
  • Humans
  • Male
  • Prostatic Neoplasms (genetics)
  • Receptors, Androgen (genetics)
  • Transcription, Genetic

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