PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 30038944-1 2018 Recent work suggests the selective Cox-2 inhibitor celecoxib delays progression to androgen independence in hormone sensitive prostate cancer (HSPC) through inhibition of the androgen receptor (AR) and ErbB signaling. Celecoxib 51-60 androgen receptor Homo sapiens 175-192 12917209-0 2003 The cyclooxygenase 2-specific nonsteroidal anti-inflammatory drugs celecoxib and nimesulide inhibit androgen receptor activity via induction of c-Jun in prostate cancer cells. Celecoxib 67-76 androgen receptor Homo sapiens 100-117 30038944-1 2018 Recent work suggests the selective Cox-2 inhibitor celecoxib delays progression to androgen independence in hormone sensitive prostate cancer (HSPC) through inhibition of the androgen receptor (AR) and ErbB signaling. Celecoxib 51-60 androgen receptor Homo sapiens 194-196 28450158-7 2017 Lastly, Celecoxib directly regulated AR transcription and translation independent of ErbB activation by downregulating the RNA binding protein heterogeneous nuclear ribonucleoprotein K (hnRNP K). Celecoxib 8-17 androgen receptor Homo sapiens 37-39 28450158-0 2017 The ErbB family and androgen receptor signaling are targets of Celecoxib in prostate cancer. Celecoxib 63-72 androgen receptor Homo sapiens 20-37 28450158-2 2017 The purpose of this work was to determine the ability of the COX-2 inhibitor Celecoxib to modulate the EGFR-AR signaling pathway in androgen-dependent PCa cells and to provide a rationale for its beneficial use in chemopreventive strategies. Celecoxib 77-86 androgen receptor Homo sapiens 108-110 28450158-8 2017 The simultaneous suppression of ErbB kinases and androgen signaling by Celecoxib represents a novel strategy to interrupt the vicious cycle of AR/ErbB cross-talk with the primary purpose of undermining their resilient signaling in prostate cancer progression. Celecoxib 71-80 androgen receptor Homo sapiens 143-145 24518515-0 2014 EP2 signaling mediates suppressive effects of celecoxib on androgen receptor expression and cell proliferation in prostate cancer. Celecoxib 46-55 androgen receptor Homo sapiens 59-76 27105861-0 2016 Pharmacokinetic drug interactions of the selective androgen receptor modulator GTx-024(Enobosarm) with itraconazole, rifampin, probenecid, celecoxib and rosuvastatin. Celecoxib 139-148 androgen receptor Homo sapiens 51-68 24518515-6 2014 RESULTS: Celecoxib induced apoptosis and downregulated EP2, CREB and androgen receptor (AR). Celecoxib 9-18 androgen receptor Homo sapiens 69-86 24518515-6 2014 RESULTS: Celecoxib induced apoptosis and downregulated EP2, CREB and androgen receptor (AR). Celecoxib 9-18 androgen receptor Homo sapiens 88-90 24518515-8 2014 Furthermore, EP2 and CREB knockdown induced AR downregulation, indicating that AR suppression by celecoxib is mediated by EP2/CREB signaling. Celecoxib 97-106 androgen receptor Homo sapiens 44-46 24518515-8 2014 Furthermore, EP2 and CREB knockdown induced AR downregulation, indicating that AR suppression by celecoxib is mediated by EP2/CREB signaling. Celecoxib 97-106 androgen receptor Homo sapiens 79-81 24518515-9 2014 CONCLUSIONS: Celecoxib exerts antitumor activity through EP2 signaling regulating AR and COX-2 expression. Celecoxib 13-22 androgen receptor Homo sapiens 82-84