J4 ›› 2010, Vol. 36 ›› Issue (3): 453-455.
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REN Meng, LIU Lu-Cheng, WEI Wei, LI Zhi, ZHANG Ming, WEN Dou-Su
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Abstract:Objective To investigate the influence and effect of rAV-Tumstatin on T24 cell lines,and provide experimental basis for further study on its mechanism.Methods rAV-Tumstatin was constructed and the T24 cell lines were infected.The cells were divided into rAV-Tumstatin group,vacant viral infection group and control group.The proliferation and apoptosis of the infected cells were detected by MTT and TUNEL.Results The T24 cells could be stably infected by rAV-Tumstatin and expressed the exogenous gene EGFP. The result of TUNEL showed the apoptotic rates in rAV-Tumstatin group,vacant viral infection group and control groupwere 32.9%,13.5%,and 6.7%,respectively;there were significant differences between three groups(P<0.01).The result of MTT which detected the proliferation and growth of T24 cells respectively showed as follows: rAV-Tumstatin group,G0/G1 60.3%,S 17.4%,G2/M 21.5%;vacant viral infection group,G0/G1 45.2%,S 29.5%,G2/M 24.8%; control group,G0/G1 43.7%,S 32.8%,G2/M 23.7%;there were also significant differences between three groups(P<0.05).Conclusion rAV-Tumstatin can inhibit the proliferation and induce the apoptosis of T24 cells,and it is very valuable for the gene therapy of bladder cancer.
Key words: bladder neoplasms;recombinant adenovirus;Tumstatin
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REN Meng, LIU Lu-Cheng, WEI Wei, LI Zhi, ZHANG Ming, WEN Dou-Su. Construction of rAV-Tumstatin viral vector and detection of its bioactivty[J].J4, 2010, 36(3): 453-455.
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http://xuebao.jlu.edu.cn/yxb/EN/Y2010/V36/I3/453
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