PMID- 17199135 OWN - NLM STAT- MEDLINE DCOM- 20070716 LR - 20070601 IS - 1365-7852 (Print) IS - 1365-7852 (Linking) VI - 10 IP - 2 DP - 2007 TI - Global analysis of differentially expressed genes in androgen-independent prostate cancer. PG - 167-74 AB - Progression to androgen independent (AI) is the main cause of death in prostate cancer, and the mechanism is still unclear. By reviewing the expression profiles of 26 prostate cancer samples in a holistic view, we found a group of genes differentially expressed in AI compared with androgen-dependent groups (P-value<0.01, t-test). Focusing on apoptosis, proliferation, hormone and angiogenesis, we found a group of genes such as thioredoxin domain containing 5 , tumor necrosis factor receptor superfamily, member 10a , ribosomal protein S19 and Janus kinase 2 upregulated in AI prostate cancer, could play important roles in the transition from AD to AI and could be biomarkers of prognosis. FAU - Wei, Q AU - Wei Q AD - State Key Laboratory of Genetic Engineering, Institute of Genetics, School of Life Science, Fudan University, Shanghai, PR China. FAU - Li, M AU - Li M FAU - Fu, X AU - Fu X FAU - Tang, R AU - Tang R FAU - Na, Y AU - Na Y FAU - Jiang, M AU - Jiang M FAU - Li, Y AU - Li Y LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20070102 PL - England TA - Prostate Cancer Prostatic Dis JT - Prostate cancer and prostatic diseases JID - 9815755 RN - 0 (Androgen Antagonists) RN - 0 (Androgens) SB - IM MH - Androgen Antagonists/pharmacology MH - Androgens/pharmacology MH - Gene Expression Profiling MH - Humans MH - Male MH - Oligonucleotide Array Sequence Analysis MH - Prostatic Neoplasms/*genetics/*metabolism EDAT- 2007/01/03 09:00 MHDA- 2007/07/17 09:00 CRDT- 2007/01/03 09:00 PHST- 2007/01/03 09:00 [pubmed] PHST- 2007/07/17 09:00 [medline] PHST- 2007/01/03 09:00 [entrez] AID - 4500933 [pii] AID - 10.1038/sj.pcan.4500933 [doi] PST - ppublish SO - Prostate Cancer Prostatic Dis. 2007;10(2):167-74. doi: 10.1038/sj.pcan.4500933. Epub 2007 Jan 2.