PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 19622577-0 2009 Transcriptional repression and inhibition of nuclear translocation of androgen receptor by diallyl trisulfide in human prostate cancer cells. diallyl trisulfide 91-109 androgen receptor Homo sapiens 70-87 19622577-1 2009 PURPOSE: The present study was undertaken to determine the effect of diallyl trisulfide (DATS), a promising cancer chemopreventive constituent of garlic, on androgen receptor (AR) protein expression and function using prostate cancer cells. diallyl trisulfide 69-87 androgen receptor Homo sapiens 157-174 19622577-1 2009 PURPOSE: The present study was undertaken to determine the effect of diallyl trisulfide (DATS), a promising cancer chemopreventive constituent of garlic, on androgen receptor (AR) protein expression and function using prostate cancer cells. diallyl trisulfide 89-93 androgen receptor Homo sapiens 157-174 19622577-3 2009 The effect of DATS treatment on AR mRNA level and AR promoter activity was determined by quantitative reverse transcription-PCR and luciferase reporter assay, respectively. diallyl trisulfide 14-18 androgen receptor Homo sapiens 32-34 19622577-3 2009 The effect of DATS treatment on AR mRNA level and AR promoter activity was determined by quantitative reverse transcription-PCR and luciferase reporter assay, respectively. diallyl trisulfide 14-18 androgen receptor Homo sapiens 50-52 19622577-7 2009 RESULTS: Exposure of prostate cancer cells (LNCaP, C4-2, and TRAMP-C1) to DATS resulted in a concentration-dependent decrease in protein level of AR, which was accompanied by suppression of intracellular and secreted levels of PSA. diallyl trisulfide 74-78 androgen receptor Homo sapiens 146-148 19622577-8 2009 Structure-activity studies revealed critical roles for allyl groups and the oligosulfide chain length in DATS-mediated down-modulation of AR protein. diallyl trisulfide 105-109 androgen receptor Homo sapiens 138-140 19622577-12 2009 CONCLUSION: The present study shows, for the first time, that DATS treatment suppresses AR function in prostate cancer cells. diallyl trisulfide 62-66 androgen receptor Homo sapiens 88-90