期刊文献+

Adenovirus-mediated Transfer of p53 and p16Inhibiting Proliferating Activity of Human Bladder Cancer Cell EJin vitro and in vivo

Adenovirus-mediated Transfer of p53 and p16Inhibiting Proliferating Activity of Human Bladder Cancer Cell EJin vitro and in vivo
下载PDF
导出
摘要 To evaluate the effects of adenovirus (Ad) - mediated transfer of p5 3and p16 on hum an bladder cancer cells EJ,EJwere transfected with Ad- p5 3and Ad- p16 . Cell growth,m orphologi- cal change,cell cycle,apoptosis were measured using MTT assay,flow cytom etry,cloning form a- tion,im munocytochemical assays.Ad- p16 or Ad- p5 3alone could inhibit the proliferating activity of EJcells in vitro.Ad- p5 3could induce apoptosis of partial EJcells.G1arrest was observed72 h after infection with Ad- p16 ,but apoptosis was not obvious.The transfer of Ad- p16 and Ad- p5 3 could significantly inhibit the growth of EJcells,decrease the cloning formation rate and induce apoptosis of large num ber of EJcells. The occurrence time of subcutaneous tumor was delayed and the tum or volume in 4 weeks was dim inished by using Ad- p5 3com bined with Ad- p16 and the dif- ference was significant com pared with using Ad- p5 3or Ad- p16 alone.It was suggested that the transfer of wild- type p5 3and p16 could significantly inhibit the growth of human bladder cancer in vitro and in vivo. To evaluate the effects of adenovirus (Ad) - mediated transfer of p5 3and p16 on hum an bladder cancer cells EJ,EJwere transfected with Ad- p5 3and Ad- p16 . Cell growth,m orphologi- cal change,cell cycle,apoptosis were measured using MTT assay,flow cytom etry,cloning form a- tion,im munocytochemical assays.Ad- p16 or Ad- p5 3alone could inhibit the proliferating activity of EJcells in vitro.Ad- p5 3could induce apoptosis of partial EJcells.G1arrest was observed72 h after infection with Ad- p16 ,but apoptosis was not obvious.The transfer of Ad- p16 and Ad- p5 3 could significantly inhibit the growth of EJcells,decrease the cloning formation rate and induce apoptosis of large num ber of EJcells. The occurrence time of subcutaneous tumor was delayed and the tum or volume in 4 weeks was dim inished by using Ad- p5 3com bined with Ad- p16 and the dif- ference was significant com pared with using Ad- p5 3or Ad- p16 alone.It was suggested that the transfer of wild- type p5 3and p16 could significantly inhibit the growth of human bladder cancer in vitro and in vivo.
出处 《Journal of Huazhong University of Science and Technology(Medical Sciences)》 SCIE CAS 2002年第4期324-326,共3页 华中科技大学学报(医学英德文版)
基金 Thisprojectwassupported by a grant from 86 3Project ofChina(No.Z2 0 - 0 1- 0 2 )
关键词 p5 3 P16 bladder cancer ADENOVIRUS p5 3 p16 bladder cancer adenovirus
  • 相关文献

参考文献5

  • 1Tokunaga H,Shariat S F,Green A E et al.Correlation of immunohistochemical molecular staging of bladder biopsies and radical cystectomy specimens[].International Journal of Radiation Oncology Biology Physics.2001
  • 2Volker S,Karsten B,Susanne H et al.Adenovirally transferred p16INK4 CDKN2 and p53 genes cooperate to induce apoptotic tumor cell death[].Nature Medicine.1997
  • 3Lukas J.p16, but not constitutively active pRb, can impose a sustained G1 arrest : molecular mechanisms and implications for oncogenesis[].Oncegene.1999
  • 4Wu Q,Possati L,Montesi M et al.Growth arrest and suppression of tumorigenicity of bladder -carcinoma cell lines induced by the p16 CDKN2 (p16INK4A, MTS1)gene and other loci on human chromosome 9[].International Journal of Cancer.1996
  • 5Ghaneh P,Greenhalf W,Humphreys M et al.Adenovirus-mediated transfer of p53 and p16 (INK4a ) results in pancreatic cancer regression in vitro and in vivo[].Gene Therapy.2001

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部