基础医学与临床 ›› 2012, Vol. 32 ›› Issue (10): 1132-1136.

• 研究论文 • 上一篇    下一篇

PARG基因沉默对小鼠结肠癌CT26细胞肝转移影响

杨怡1,王娅兰2,王洁琼1,盛永涛1   

  1. 1. 重庆医科大学 病理学教研室 分子医学与肿瘤研究中心
    2. 重庆医科大学
  • 收稿日期:2011-09-27 修回日期:2012-01-02 出版日期:2012-10-05 发布日期:2012-09-28
  • 通讯作者: 王娅兰 E-mail:wangyalan074@126.com
  • 基金资助:
    parg对pi3k/akt 和mapk蛋白激酶级联反应的影响在大肠癌转移中的作用

Effect of Poly(ADP-ribose) glycohydrolase (PARG) gene silencing on liver metastasis of colorectal carcinoma CT26 cell line in mice

  • Received:2011-09-27 Revised:2012-01-02 Online:2012-10-05 Published:2012-09-28
  • Contact: Ya-lan WANG E-mail:wangyalan074@126.com

摘要: 摘要:目的 探讨多聚(腺苷二磷酸核糖)水解酶(PARG)基因沉默对小鼠结肠癌CT26细胞肝脏转移的影响。方法 小鼠随机分成3组,脾脏包膜下注射PARG-shRNA慢病毒载体转染CT26细胞悬液,以未转染组和空载体转染组为对照。比较各组脾脏肝脏瘤结节数量、大小;Western blot检测PARG、PARP、NF-κB、integrin-β1、MMP-2和MMP-9的表达。结果 PARG基因沉默组小鼠脾脏移植瘤大小及肝脏转移瘤结节分级均明显低于对照组(P<0.05);PARG基因沉默后,脾脏移植瘤组织中PARG(0.0105±0.0028)、PARP(0.1786±0.024)、NF-κB(0.1678±0.0359)、integrin-β1、MMP-2和MMP-9的蛋白表达量明显低于对照组(P<0.05)。结论 PARG基因沉默后能抑制小鼠脾脏移植瘤的生长及肝脏转移瘤结节的形成,其作用可能是通过下调PARP、 NF-κB及其下游依赖性基因的表达而实现的。

关键词: PARG-shRNA, 结肠癌, 肝转移

Abstract: Abstract:Objective This study was to investigate the effect of PARG-shRNA on liver metastasis of colorectal carcinoma CT26 cell line in mice. Methods Mice were divided at random into three groups. Animal models for Liver metastases of colorectal cancer were established by intrasplenic inoculation of colorectal carcinoma cell in BALB/c mice.CT26 cells transfected with empty vector and CT26 cells transfected with PARG-shRNA were inoculated to spleen caspsule.CT26 cells transfected with empty vector and untransfected CT26 cells served as control. The change of spleen and liver metastases carcinoma nodules were observed and counted. The expressions of PARG, PARP, NF-κB, integrin-β1,MMP-2,MMP-9 in spleen transplant tumor were measured by Western blot analysis. Results The size of spleen transplant tumor and liver metastatic nodules in transfected group were smaller than that in the control groups (p<0.05). The expression of PARG(0.0105±0.0028)、PARP(0.1786±0.024)、NF-κB(0.1678±0.0359)、integrin-β1、MMP-2、MMP-9 in transfected group was weaker than that in the control groups (p<0.05). Conclusion The growth of spleen transplant tumor and liver metastases can be inhibited by PARG gene silencing in CT26 cells. It is probably through inhibiting PARP, NF-κB and NF-κB-dependent gene downstream.

Key words: PARG-shRNA, colon carcinoma, liver metastases

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