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pmid26110567      Oncotarget 2015 ; 6 (25): 21120-36
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  • By inhibiting snail signaling and miR-23a-3p, osthole suppresses the EMT-mediated metastatic ability in prostate cancer #MMPMID26110567
  • Wen YC; Lee WJ; Tan P; Yang SF; Hsiao M; Lee LM; Chien MH
  • Oncotarget 2015[Aug]; 6 (25): 21120-36 PMID26110567show ga
  • Here we showed that Osthole, 7-methoxy-8-(3-methyl-2-butenyl) coumarin, a bioactive coumarin derivative extracted from medicinal plants, inhibited migration, invasion, epithelial to mesenchymal transition (EMT) in androgen-independent prostate cancer (AIPC) cells in vitro and metastasis of AIPC in vivo. In patients, high Snail levels were correlated with a higher histological Gleason sum and poor survival rates. Osthole inhibited the TGF-?/Akt/MAPK pathways, reduced Snail-DNA-binding activity and induced E-cadherin. We found that osthole decreased miR-23a-3p. Ectopic miR-23a-3p suppressed E-cadherin 3? untranslated region reporter activity and E-cadherin expression, and relieved the motility suppression caused by osthole treatment.
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