Objective:To investigate the effects and mechanisms of Nimesulide on proliferation inhuman hepatocellular carcinoma HepG2cells under the hypoxia environment.Contents and methods of research:HepG2cells were divided into6groups:normaxia(21%O2)+cells with notreatment,nomaxia+cells with50μmol/L Nimesulide,hypoxia(1%O2)+cells with notreatment, hypoxia+cells with50μmol/L Nimesulide, hypoxia+cells with100μmol/LNimesulide, hypoxia+cells with200μmol/L Nimesulide.The cell proliferation wasexamined by methyl thiazolyl tetrazolium(MTT) assay.The expression levels ofcyclooxygenase-2(COX-2),HIF-1α and survivin mRNA were detected byRT-PCR.The COX-2,HIF-1α and survivin protein expression were measured byWestern blotting.Results:Nimesulide inhibited the proliferation of the HepG2under the hypoxiaenvironment.Compared with cells under nomarxia environment,the expression ofCOX-2,HIF-1α and survivin of the cells under hypoxia environment werehigher(P<0.05).Compared with the hypoxia(1%O2)+cells with no treatmentgroup,the expression levels of COX-2and survivin mRNA of HepG2were obviouslower in the treatment group(P<0.05),the expression levels of COX-2,HIF-1α andsurvivin protein were significantly decreased(P<0.05).Conclusion:Nimesulide can inhibit proliferation on HepG2cells.The possible mechanismsare given below, Nimesulide can inhibit the activity of COX-2or reduce theexpression of HIF-1α protein. |