PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 29877111-0 2019 PEITC promotes neurite growth in primary sensory neurons via the miR-17-5p/STAT3/GAP-43 axis. phenethyl isothiocyanate 0-5 microRNA 17 Homo sapiens 65-74 29877111-6 2019 To further determine a substitution therapy for sciatic nerve conditioning injury, beta-phenethyl isothiocyanate (PEITC), which downregulates miR-17-5p, was assessed. phenethyl isothiocyanate 83-112 microRNA 17 Homo sapiens 142-151 29877111-6 2019 To further determine a substitution therapy for sciatic nerve conditioning injury, beta-phenethyl isothiocyanate (PEITC), which downregulates miR-17-5p, was assessed. phenethyl isothiocyanate 114-119 microRNA 17 Homo sapiens 142-151 29877111-8 2019 Further experiments demonstrated PEITC induced neurite growth by inhibiting miR-17-5p and further upregulating STAT3, p-STAT3 and GAP-43. phenethyl isothiocyanate 33-38 microRNA 17 Homo sapiens 76-85 29877111-11 2019 PEITC could promote repair of injured dorsal column via the miR-17-5p/STAT3/GAP-43 axis, and could mimic the treatment effect of sciatic nerve conditioning injury. phenethyl isothiocyanate 0-5 microRNA 17 Homo sapiens 60-69 23661605-8 2013 PEITC treatment significantly decreased PCAF expression and promoted transcription of miR-17 in LNCaP cells. phenethyl isothiocyanate 0-5 microRNA 17 Homo sapiens 86-92 24732804-2 2014 Here we demonstrate that PEITC-induced ROS decreased expression of microRNA 27a (miR-27a)/miR-20a:miR-17-5p and induced miR-regulated ZBTB10/ZBTB4 and ZBTB34 transcriptional repressors, which, in turn, downregulate specificity protein (Sp) transcription factors (TFs) Sp1, Sp3, and Sp4 in pancreatic cancer cells. phenethyl isothiocyanate 25-30 microRNA 17 Homo sapiens 98-107 24732804-3 2014 Decreased expression of miR-27a/miR-20a:miR-17-5p by PEITC-induced ROS is a key step in triggering the miR-ZBTB Sp cascade leading to downregulation of Sp TFs, and this is due to ROS-dependent epigenetic effects associated with genome-wide shifts in repressor complexes, resulting in decreased expression of Myc and the Myc-regulated miRs. phenethyl isothiocyanate 53-58 microRNA 17 Homo sapiens 40-49 23661605-9 2013 Functional inhibition of miR-17 attenuated the suppression of PCAF in cells treated by PEITC. phenethyl isothiocyanate 87-92 microRNA 17 Homo sapiens 25-31 23661605-10 2013 CONCLUSION: Our results indicate that PEITC inhibits AR-regulated transcriptional activity and cell growth of PCa cells through miR-17-mediated suppression of PCAF, suggesting a new mechanism by which PEITC modulates PCa cell growth. phenethyl isothiocyanate 38-43 microRNA 17 Homo sapiens 128-134 23661605-10 2013 CONCLUSION: Our results indicate that PEITC inhibits AR-regulated transcriptional activity and cell growth of PCa cells through miR-17-mediated suppression of PCAF, suggesting a new mechanism by which PEITC modulates PCa cell growth. phenethyl isothiocyanate 201-206 microRNA 17 Homo sapiens 128-134