PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 22052438-0 2012 Cryptotanshinone down-regulates androgen receptor signaling by modulating lysine-specific demethylase 1 function. cryptotanshinone 0-16 androgen receptor Homo sapiens 32-49 22052438-3 2012 In our study, we showed that cryptotanshinone inhibited the growth of AR-positive prostate cancer cells, suggesting that cryptotanshinone affected AR function. cryptotanshinone 29-45 androgen receptor Homo sapiens 70-72 22052438-3 2012 In our study, we showed that cryptotanshinone inhibited the growth of AR-positive prostate cancer cells, suggesting that cryptotanshinone affected AR function. cryptotanshinone 29-45 androgen receptor Homo sapiens 147-149 22052438-3 2012 In our study, we showed that cryptotanshinone inhibited the growth of AR-positive prostate cancer cells, suggesting that cryptotanshinone affected AR function. cryptotanshinone 121-137 androgen receptor Homo sapiens 70-72 22052438-3 2012 In our study, we showed that cryptotanshinone inhibited the growth of AR-positive prostate cancer cells, suggesting that cryptotanshinone affected AR function. cryptotanshinone 121-137 androgen receptor Homo sapiens 147-149 22052438-4 2012 Cryptotanshinone also profoundly inhibited the transcriptional activity of AR and suppressed the expression of several AR-target genes at the mRNA and the protein levels. cryptotanshinone 0-16 androgen receptor Homo sapiens 75-77 22052438-4 2012 Cryptotanshinone also profoundly inhibited the transcriptional activity of AR and suppressed the expression of several AR-target genes at the mRNA and the protein levels. cryptotanshinone 0-16 androgen receptor Homo sapiens 119-121 22052438-5 2012 At the molecular level, cryptotanshinone disrupted the interaction between AR and lysine-specific demethylase 1 (LSD1), and inhibited the complex of AR and LSD1 to the promoter of AR target genes without affecting the protein degradation and translocation of AR. cryptotanshinone 24-40 androgen receptor Homo sapiens 75-77 22052438-5 2012 At the molecular level, cryptotanshinone disrupted the interaction between AR and lysine-specific demethylase 1 (LSD1), and inhibited the complex of AR and LSD1 to the promoter of AR target genes without affecting the protein degradation and translocation of AR. cryptotanshinone 24-40 androgen receptor Homo sapiens 149-151 22052438-5 2012 At the molecular level, cryptotanshinone disrupted the interaction between AR and lysine-specific demethylase 1 (LSD1), and inhibited the complex of AR and LSD1 to the promoter of AR target genes without affecting the protein degradation and translocation of AR. cryptotanshinone 24-40 androgen receptor Homo sapiens 149-151 22052438-5 2012 At the molecular level, cryptotanshinone disrupted the interaction between AR and lysine-specific demethylase 1 (LSD1), and inhibited the complex of AR and LSD1 to the promoter of AR target genes without affecting the protein degradation and translocation of AR. cryptotanshinone 24-40 androgen receptor Homo sapiens 149-151 22052438-7 2012 These data suggest that cryptotanshinone functions via inhibition of LSD1, a protein that promotes AR-dependent transcriptional activity via derepression of H3K9. cryptotanshinone 24-40 androgen receptor Homo sapiens 99-101 22052438-8 2012 In summary, we describe a novel mechanism whereby cryptotanshinone down-regulates AR signaling via functional inhibition of LSD1-mediated demethylation of H3K9 and represses the transcriptional activity of AR. cryptotanshinone 50-66 androgen receptor Homo sapiens 82-84 22052438-8 2012 In summary, we describe a novel mechanism whereby cryptotanshinone down-regulates AR signaling via functional inhibition of LSD1-mediated demethylation of H3K9 and represses the transcriptional activity of AR. cryptotanshinone 50-66 androgen receptor Homo sapiens 206-208 22154085-0 2012 Cryptotanshinone suppresses androgen receptor-mediated growth in androgen dependent and castration resistant prostate cancer cells. cryptotanshinone 0-16 androgen receptor Homo sapiens 28-45 22154085-4 2012 Our results indicated that 0.5 muM CTS effectively suppresses the growth of AR-positive PCa cells, but has little effect on AR negative PC-3 cells and non-malignant prostate epithelial cells. cryptotanshinone 35-38 androgen receptor Homo sapiens 76-78 22154085-5 2012 Furthermore, our data indicated that CTS could modulate AR transactivation and suppress the DHT-mediated AR target genes (PSA, TMPRSS2, and TMEPA1) expression in both androgen responsive PCa LNCaP cells and castration resistant CWR22rv1 cells. cryptotanshinone 37-40 androgen receptor Homo sapiens 56-58 22154085-6 2012 Importantly, CTS selectively inhibits AR without repressing the activities of other nuclear receptors, including ERalpha, GR, and PR. cryptotanshinone 13-16 androgen receptor Homo sapiens 38-40 22154085-7 2012 The mechanistic studies indicate that CTS functions as an AR inhibitor to suppress androgen/AR-mediated cell growth and PSA expression by blocking AR dimerization and the AR-coregulator complex formation. cryptotanshinone 38-41 androgen receptor Homo sapiens 58-60 22154085-7 2012 The mechanistic studies indicate that CTS functions as an AR inhibitor to suppress androgen/AR-mediated cell growth and PSA expression by blocking AR dimerization and the AR-coregulator complex formation. cryptotanshinone 38-41 androgen receptor Homo sapiens 92-94 22154085-7 2012 The mechanistic studies indicate that CTS functions as an AR inhibitor to suppress androgen/AR-mediated cell growth and PSA expression by blocking AR dimerization and the AR-coregulator complex formation. cryptotanshinone 38-41 androgen receptor Homo sapiens 92-94 22154085-8 2012 Furthermore, we showed that CTS effectively inhibits CWR22Rv1 cell growth and expressions of AR target genes in the xenograft animal model. cryptotanshinone 28-31 androgen receptor Homo sapiens 93-95