2和1%七氟醚培養(yǎng)24 h,對照組僅以5% CO2培養(yǎng)24 h,MTT法檢測兩組細胞增殖能力的變化,Transwell侵襲及遷移實驗檢測細胞侵襲及遷移能力,Western blotting檢測兩組細胞干細胞特性相關分子(Oct4及Sox2)及上皮間充質轉化(EMT)相關分子(E-cadherin、Vimentin)的表達差異。結果 七氟醚組細胞72、96 h時間點增殖能力顯著低于對照組,差異具有統(tǒng)計學意義(P<0.05)。七氟醚組穿透Matrigel基質膠的細胞數(shù)、遷出Transwell上小室的細胞數(shù)均明顯少于對照組,差異具有統(tǒng)計學意義(P<0.05)。七氟醚組Oct4、Sox2、Vimentin表達均顯著低于對照組,E-cadherin表達顯著高于對照組,差異具有統(tǒng)計學意義(P<0.05)。結論 七氟醚可通過減輕卵巢癌細胞EMT進程及干細胞特性,抑制細胞增殖及侵襲遷移能力。;Objective To investigate the effects of sevoflurane on the characteristics of stem cells, proliferation, invasion and migration ability of ovarian cancer cell SKOV3. Methods Human ovarian cancer cells SKOV3 in culture flask were divided into sevoflurane and control group. The sevoflurane group cell was cultured under environment of 5%CO2 and 1% sevoflurane for 24 h, and the control group cell was cultured under environment of 5%CO2 for 24 h. MTT method was used to detect the ability of cell proliferation of two groups of cell. Transwell invasion and migration assay were used to detect the ability of cell invasion and migration of two groups of cell. Western blotting was used to detect the expression of stem cell related molecular (Oct4 and Sox2) and epithelial mesenchymal transition (EMT) related molecules (E-cadherin, Vimentin). Results The proliferation ability of the sevoflurane group was significantly lower than that of the control group at 72 and 96 h, and the difference was statistically significant (P<0.05). The number of sevoflurane cells through the matrigel and transwell chamber were less than control group, the difference was statistically significant (P<0.05). The expression of molecular stem cell related Oct4 and Sox2 in sevoflurane group were lower than that in control group, the difference was statistically significant (P<0.05). The expression of molecular EMT related E-cadherin and Vimentin were lower than that in control group, the difference was statistically significant (P<0.05). Conclusion Sevoflurane can inhibit the ability of proliferation, invasion and migration in ovarian cancer cells by reducing the EMT process and stem cell characteristics."/>