期刊文献+

双歧杆菌对实验性大肠癌丝裂素活化蛋白激酶和激活蛋白-1的影响 被引量:2

Effect of bifidobacteria on MAPK and AP-1 of experimental large bowel carcinoma
原文传递
导出
摘要 目的 探索青春型双歧杆菌的体内抑瘤机制。方法 以激光共聚焦显微镜检测了大肠癌裸鼠移植瘤细胞外信号调节蛋白激酶(ERK)1/2、c-jun氨基末端激酶(JNK)和p38以及激活蛋白-1(AP-1)的主要成份 c-fos和c-jun的含量。结果 大肠癌裸鼠移植瘤经双歧杆菌处理后,其ERK1/2、JNK、c-fos和c-jun的平均荧光强度均显著低于肿瘤对照组(P<0.01),而p38的平均荧光强度在两组间差异无显著性(P>0.05)。结论 青春型双歧杆菌体内能明显降低大肠癌ERK1/2和JNK的活性以及c-fos和c-jun的表达。 Objective To explore the antitumor mechanisms of bifidobacteria adolescence in vivo. Methods The content of extracellular signal regulated protein (ERK) 1/2, C-Jun N-terminal kinase (JNK), p38, c-fos and c-jun of nude mouse transplantation tumors of large bowel carcinoma was detected by using laser scanning confocal microscopy. C-fos and c-jun were the main composition of activator pro- tein 1. Results After the nude mouse transplantation tumors of large bowel carcinoma were treated with bifidobacteria, the average fluorescent intensity of ERK1/2, JNK, c-fos and c-jun was significantly lower than that in tumor control group (P < 0. 01). There was no significant difference in the average flures- cent intensity of p38 between two groups (P > 0. 05). Conclusion Bifidobacteria adolescence could markedly decrease the activity of ERK1/2, JNK and the expression of c-fos, c-jun.
出处 《中华实验外科杂志》 CAS CSCD 北大核心 2003年第12期1119-1120,共2页 Chinese Journal of Experimental Surgery
基金 广东省自然科学基金资助项目(994066)
关键词 双歧杆菌 实验 大肠癌 丝裂素活化 蛋白激酶 激活蛋白-1 Bifidobacterium Large bowel carcinoma Protein kinase
  • 相关文献

参考文献5

二级参考文献8

共引文献93

同被引文献51

  • 1梁庆红,王倩,张琳,张亚超,王沛,周志广.双歧杆菌对小鼠体液免疫功能的影响[J].承德医学院学报,2004,21(2):100-101. 被引量:8
  • 2Kozakova H, Bchakova Z, Kolinska J, Bifidobacterium Bifidum Monoassociation of Gnotobiotic Mice: Effect on Enterocyte Brush - border Enzymes[ J]. Folia Microbiol( praha),2001,46 (6) :573 - 576.
  • 3Husebye E, Hellstrom PM, Sundler F, et al. Influence of Microbial Species on Small Intestinal Myoelectric Activity and Transit in Germ -free Rats [J]. Am J Physiol Gastrointest Liver Physiol, 2001,280 (3) : 368 - 380.
  • 4MURRAYV J D,DAVIDSON L A,CHAPKIN R S,et al.Overexpression of protein kinase C beta Ⅱ induces colonic hyperproliferation and increased sensitivity to colon carcinogenesis[J].J Cell Biol 1999,145(4):699-711.
  • 5YU H G,YE L L,YANG Y N,et al.Increased expression of reIA/Nuclear factor-κB protein correlates with colorectal tumorigenesis[J].Oncology,2003,65(1):37-45.
  • 6Widmann C,GIBSON S,JARPE M B,et al.Mitogen-activated protein kinase:conservation of a three-kinase module from yeast to human[J].Physiol Rev,1999,79 (1):143-180.
  • 7CHIO C C,CHANG Y H,HSU Y W,et al.PKA-dependent activation of PKC,p38 MAPK and IKK in macrophage:implication in the induction of inducible nitric oxide synthase and interleukin-6 by dibutyryl Camp[J].Cell Signal,2004,16(5):565-575.
  • 8XIA Z,DICKENS M,RAINGEAUD J,et al.Opposing effects of ERK and JNK-p38 MAP kinases on apoptosis[J].Science,1995,270 (10):1326-1331.
  • 9REDDY B S,RIVENSON A.Inhibitory effect of Bifidobacterium longum on colon,mantrpary and liver carcinogenesis induced by 2-amino-3-methylimidazo[4,5-f]quinoline,a food mutagen[J].Cancer Res,1993,53(21):3914-3918.
  • 10HIRAYAMA K,RAFTER J.The role of probiotic bacteria in cancer prevention[J].Microbes Infect,2000,2 (6):681-686.

引证文献2

二级引证文献24

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