安徽医科大学学报
安徽醫科大學學報
안휘의과대학학보
ACTA UNIVERSITY MEDICINALIS ANHUI
2013年
11期
1304-1307
,共4页
刘升学%孙文国%白先忠%覃展偶%张天禹
劉升學%孫文國%白先忠%覃展偶%張天禹
류승학%손문국%백선충%담전우%장천우
维生素C%膀胱癌%T-24细胞%增殖%凋亡
維生素C%膀胱癌%T-24細胞%增殖%凋亡
유생소C%방광암%T-24세포%증식%조망
vitamin C%bladder cancer%T-24%proliferation%apoptosis
目的观察不同浓度维生素C(Vit C)对膀胱癌T-24细胞增殖和凋亡的影响,并了解其可能的机制。方法使用不同浓度Vit C干预体外培养的膀胱癌T-24细胞,然后通过缩胆囊素八肽(CCK-8)检测T-24细胞增殖情况,用流式细胞术检测细胞周期的变化及其凋亡率结果,RT-PCR法检测Survivin mRNA、Caspase-3 mRNA的表达。结果400μg/ml Vit C可将T-24细胞阻滞于S期,诱导其凋亡并且下调Sur-vivin mRNA 的表达、上调 Caspase-3 mRNA 的表达。4、40μg/ml的Vit C对人膀胱癌T-24细胞无明显抑制增殖作用,而400μg/ml Vit C对人膀胱癌T-24细胞增殖有显著抑制作用。结论400μg/ml Vit C可抑制T-24细胞增殖、诱导其凋亡,其机制可能与下调Survivin mRNA表达、上调Caspase-3 mRNA表达有关。
目的觀察不同濃度維生素C(Vit C)對膀胱癌T-24細胞增殖和凋亡的影響,併瞭解其可能的機製。方法使用不同濃度Vit C榦預體外培養的膀胱癌T-24細胞,然後通過縮膽囊素八肽(CCK-8)檢測T-24細胞增殖情況,用流式細胞術檢測細胞週期的變化及其凋亡率結果,RT-PCR法檢測Survivin mRNA、Caspase-3 mRNA的錶達。結果400μg/ml Vit C可將T-24細胞阻滯于S期,誘導其凋亡併且下調Sur-vivin mRNA 的錶達、上調 Caspase-3 mRNA 的錶達。4、40μg/ml的Vit C對人膀胱癌T-24細胞無明顯抑製增殖作用,而400μg/ml Vit C對人膀胱癌T-24細胞增殖有顯著抑製作用。結論400μg/ml Vit C可抑製T-24細胞增殖、誘導其凋亡,其機製可能與下調Survivin mRNA錶達、上調Caspase-3 mRNA錶達有關。
목적관찰불동농도유생소C(Vit C)대방광암T-24세포증식화조망적영향,병료해기가능적궤제。방법사용불동농도Vit C간예체외배양적방광암T-24세포,연후통과축담낭소팔태(CCK-8)검측T-24세포증식정황,용류식세포술검측세포주기적변화급기조망솔결과,RT-PCR법검측Survivin mRNA、Caspase-3 mRNA적표체。결과400μg/ml Vit C가장T-24세포조체우S기,유도기조망병차하조Sur-vivin mRNA 적표체、상조 Caspase-3 mRNA 적표체。4、40μg/ml적Vit C대인방광암T-24세포무명현억제증식작용,이400μg/ml Vit C대인방광암T-24세포증식유현저억제작용。결론400μg/ml Vit C가억제T-24세포증식、유도기조망,기궤제가능여하조Survivin mRNA표체、상조Caspase-3 mRNA표체유관。
Objective To observe the effects of different concentrations of vitamin C (Vit C) on the proliferation and apoptosis in bladder cancer cell T-24 cells and explore its possible mechanism. Methods Different concentra-tions of Vit C were used to intervene in vitro T-24 cells. Cholecystokinin Octapeptolecyst (CCK-8) was detected to show the proliferous situation of T-24 cells. Flow cytometry was used to detect cell cycle changes and apoptosis rate and RT-PCR was used to detect the expressions of Survivin mRNA and Caspase-3 mRNA. Results 400μg/ml Vit C blocked T-24 cells in S phase, induced the apoptosis, reduced the Survivin mRNA expression and raised the Caspase-3 mRNA expression. 4 μg/ml and 40 μg/ml concentrations of Vit C did not play a significant inhibitory role in the proliferation in T-24 cells but 400 μg/ml of Vit C had significant inhibitory effects on the proliferation of T-24 cells. Conclusion 400 μg/ml Vit C can inhibit the proliferation of T-24 cells and induce the apoptosis. The possible mechanism is that Vit C reduces the expressions of Survivin mRNA, and promotes the expression of Caspase-3 mRNA.