Basic & Clinical Medicine ›› 2008, Vol. 28 ›› Issue (10): 1009-1014.

• 研究论文 • Previous Articles     Next Articles

Arsenic trioxide inhibition of the phosphorylation of P27kip threonine residue 187 in human hepatic carcinoma cell

You WANG, Mu-dan LU, Peng LI, Xiao-peng CUI, Ai-guo SHEN   

  • Received:2007-11-19 Revised:2008-01-24 Online:2008-10-25 Published:2008-10-25
  • Contact: Ai-guo SHEN

Abstract: Objective To investigate the relationship between growth inhibitory effect of arsenic trioxide(As2O3) and phosphorylation of P27kip threonine residue 187(P27T187) in human hepatocellular carcinoma(HCC) cell line SMMC-7721. Methods Cultured in vitro, SMMC-7721 were treated for 72h with 2μmol/L As2O3. The cell growth inhibition was detected by cell number counting and the cell cycle was detected by flow cytometry(FCM).The expression and localization of P27, T187 phosphorylated P27(p-P27T187) were detected by Subcellular Fractionation , Western blot and immunoflurescence. Results As2O3 significantly inhibited the proliferation of SMMC-7721 cell and cell cycle was arrested in G2/M. A striking decrease in p-P27T187 expression and a reciprocal increase in P27 expression were found in 2μmol/L As2O3-treated SMMC-7721 cell. Meanwhile, As2O3 decreased the protein levels of Cdk2 and cyclinE .The location of P27 was transferred from cytoplasm to nuclei and the expression of p-P27T187 was decreased in nuclei. Conclusion As2O3 inhibit the phosphorylation of P27T187, thereby promoting P27 accumulation in SMMC-7721 cell nuclei, inducing cel1 cycle arrest and growth inhibition.