期刊文献+

MAPK反义寡核苷酸对肝癌细胞恶性表型的逆转作用 被引量:2

Reversal of malignant phenotype of SMMC- 7721 cells by MAPK antisense oligodeoxynucleotide
下载PDF
导出
摘要 目的:探讨MAPK反义寡核苷酸对肝癌细胞恶性表型的逆转作用。方法:用脂质体转染法将MAPK反义寡核苷酸导入肝癌细胞株SMMC-7721中,通过细胞活力、蛋白质含量、集落形成和DNA合成的变化检测MAPK反义寡核苷酸对肝癌恶性表型的逆转作用。结果:MAPK反义寡核苷酸可明显抑制细胞活力、蛋白质含量、集落形成和DNA合成,其抑制率分别为52.6%、50.5%、54.9%和47.5%,与对照组比较差异有显著性(P<0.01)。结论:MAPK反义寡核苷酸可逆转SMMC-7721细胞恶性表型,也为肝癌治疗指出了新方向。 Objective To study the reversal effect of MAPK antisense oligodeoxynucleotide (ASO) on SMMC-7721 ceils. Methods After MAPK ASO was introduced into SMMC-7721 cells by liposomal transfection,the effect was evaluated by ceil viability ,protein content,colony formation and DNA synthesis. Results The cell viability, protein content, colony formation and DNA synthesis were signiilcanfly inhibited by MAPK ASO, the inhibitory rate was 52. 6%, 50.5% , 54. 9% and 47.5% respectively( P 〈 0.01) . Conclusion MAPK ASO can reverse the malignant phenotype of SMMC-7721 ceils, which may be use as a new approach in the treatment of liver cancer.
出处 《实用医学杂志》 CAS 2005年第19期2116-2118,共3页 The Journal of Practical Medicine
关键词 肝肿瘤 蛋白激酶类 寡核苷酸类 反义 逆转 反义寡核苷酸 细胞恶性表型 肝癌细胞株 MAPK 逆转作用 SMMC-7721 Liver Neoplasms Protein kinase Oligonucleotides, Antisense Reversion
  • 相关文献

参考文献8

  • 1Kohmura K, Miyakawa Y,Kawai Y,et al. Different roles of p38 MAPK and ERK in STI571-induced multi-lineage differentiation of K562 cells. J Cell Physiol,2004,198(3):370-376. 被引量:1
  • 2Locker J.A new way to look at liver cancer. Hepatology,2004,40(3):521-523. 被引量:1
  • 3Carloni V, Mazzocca A, Ravichandran KS.Tetraspanin CD81 is linked to ERK/MAPKinase signaling by Shc in liver tumor cells. Oncogene,2004,23(8):1566-1574. 被引量:1
  • 4Huang SL, Ding B, Shan B, et al.Prevention of intima hyperplasia by mitogen-activated protein kinase antisense oligodeoxynucleotide.Acta Pharmacol Sin,2000,21(4):313-317. 被引量:1
  • 5司徒镇强,吴军正主编..细胞培养[M],1996:363.
  • 6Lai EC. Notch signaling:control of cell communication and cell fate.Development,2004,131(5):965-973. 被引量:1
  • 7Lejeune D, Dumoutier L, Constantinescu S, et al. Interleukin-22 (IL-22)activates the JAK/STAT, ERK, JNK, and p38 MAP kinase pathways in a rat hepatoma cell line. Pathways that are shared with and distinct from IL-10. J Biol Chem,2002,277(37):33676-33682. 被引量:1
  • 8尚振川,孙秉中,陈志南,王玮,冯琦,王莎,张涛.MAPK反义寡核苷酸对K562细胞系的增殖抑制作用[J].第四军医大学学报,2003,24(14):1259-1261. 被引量:2

二级参考文献3

共引文献1

同被引文献28

引证文献2

二级引证文献20

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