AIM:To investigate the effect of knockdown of forkhead box M1(foxM1)on the proliferation and invasion capacities of human gallbladder carcinoma(Gbc)-sd cells.METHODS:four foxM1 shRNAs were transfected into Gbc-sd cells with lipofectamine 2000 to select the appropriate shRNA for down-regulation of foxM1.A recombinant lentivirus for shfoxM1(lv-shfoxM1),which expresses FoxM1-specific shRNA,and a negative control carrying green fluorescent protein,which expresses a scrambled RNA,were constructed.After transfection with the recombinant adenovirus and screened with puromycin,RT-PcR and Western blot were utilized to evaluate the inhibition efficiency.cell viability was evaluated by MTT assay,and cell migration and invasion were assessed using the Transwell system.cells were suspended in serum-free medium and seeded into Transwell inserts either uncoated(for migration assay)or coated(for invasion assay)with growth factor-reduced Matrigel.To verify the involvement of foxM1 in the senescence of tumor cells,staining of senescenceβ-galactosidase(sAβ-gal),the widely used biomarker of cellular senescence,was also performed.RESULTS:After successful transfection of four foxM1small interfering RNAs(shRNAs)with lipofectamine2000,the shf1822 was selected as the most appropriate shRNA according to its obvious inhibitory effect.The recombinant adenovirus was then constructed with the shf1822 and successfully transfected into the Gbcsd cells,resulting in the significant inhibition of foxM1expression at both the mRNA and protein levels,compared with the negative control(P<0.05).After transfection,down-regulation of foxM1 significantly inhibited cell viability according to the MTT assay(P<0.05).In addition,Transwell migration and invasion assays also suggested the suppression of invasion ability of the transfected cells.sAβ-gal staining showed that downregulation of foxM1 could induce more senescent Gbc cells(P<0.05),suggesting the possible involvement of the senescence process of the foxM1-deficient cells in Gbc.CONCLUSION:foxM1 is functionally involved in viability of Gbc cells,partially dependent on the inducement of cellular senescence,and is a potential target for Gbc therapy. AIM: To investigate the effect of knockdown of forkhead box M1 (foxM1) on the proliferation and invasion vectors of human gallbladder carcinoma (Gbc) -sd cells. METHODS: four foxM1 shRNAs were transfected into Gbc-sd cells with lipofectamine 2000 to select the suitable shRNA for down-regulation of foxM1.A recombinant lentivirus for shfoxM1 (lv-shfoxM1), which expresses FoxM1-specific shRNA, and a negative control carrying green fluorescent protein, which expresses a scrambled RNA, were constructed. After transfection with the recombinant adenovirus and screened with puromycin, RT-PcR and Western blot were utilized to evaluate the inhibition efficiency. cell viability was evaluated by MTT assay, and cell migration and invasion were assessed using the Transwell system. cells were suspended in serum-free medium and seeded into Transwell inserts either uncoated (for migration assay) or coated (for invasion assay) with growth factor-reduced Matrigel. To verify the involvement of foxM1 in the senescence of tumor cells, staining of senescence β-galactosidase (sAβ-gal), the widely used biomarker of cellular senescence, was also performed .RESULTS: After successful transfection of four foxM1small interfering RNAs (shRNAs) with lipofectamine2000, the shf1822 was selected as the most appropriate shRNA according to its obvious inhibitory effect. recombinant adenovirus was constructed with the shf1822 and successfully transfected into the Gbcsd cells, resulting in the significant inhibition of foxM1expression at both the mRNA and protein levels, compared with the negative control (P <0.05) . Transfection migration and invasion assays also suggested the suppression of invasion ability of the transfected cells. [Delta] A-gal staining showed that downregulation of foxM1 could induce more senescent Gbc cells (P <0.05), suggesting the possible involvement of the senescence process of the f oxM1-deficient cells in Gbc.CONCLUSION: foxM1 is functionally involved in viability of Gbc cells, partially dependent on the inducement of cellular senescence, and is a potential target for Gbc therapy.