期刊文献+

Id2在Apc^(Δ716/+)小鼠肠道肿瘤发生中的作用 被引量:1

The role of Id2 in the growth of intestinal tumor in Apc^(Δ716/+) mice SHEN Xiaodong
下载PDF
导出
摘要 目的研究DNA结合抑制物2(inhibitor of DNA binding 2,Id2)在ApcΔ716/+小鼠肠道肿瘤发生中的作用。方法 Id2基因缺失的基因工程小鼠和肠道肿瘤模型ApcΔ716/+小鼠杂交后,统计ApcΔ716/+小鼠与ApcΔ716/+Id2-/-杂交小鼠小肠肠道肿瘤的数目及总负荷,观查其肠道肿瘤发生和发展的变化。结果与ApcΔ716/+Id2野生型小鼠比较,ApcΔ716/+Id2-/-杂交小鼠在4、8、12周龄时肠道肿瘤总数目与不同大小的肠道肿瘤数目明显减少,差异有统计学意义(P均<0.05)。结论 Id2的缺失能抑制ApcΔ716/+小鼠肠道肿瘤的发生,Id2在人类肠道肿瘤中可能发挥着促进肿瘤形成的作用。 Objective To investigate the role of Id2 in the development and growth of intestinal tumor in ApcΔ716/+ mice. Methods ApcΔ716/+ mice were crossed with Id2 deficient mice and the tumor susceptibility in intestine was com- pared. The total intestine tumor number and the tumor number of different size of ApcΔ716/+ Id2 +/+ mice and ApcΔ716/+ Id2 /- mice were analyzed and the changes in intestinal tumor were observed. Results Compared with ld2 wild in ApcΔ716/+ mice, Id2 deficient in ApcΔ716/+ mice resulted in significant decrease of tumor total number and tumor number of different size in intestine at 4, 8 and 12 weeks, respectively (P 〈 0.05 ). Conclusion These findings have provided the genetic evidence for a tumor promotion role of Id2 in the intestine of mice. Importantly, these studies also suggest that Id2 may act as a tumor promotor for human intestinal tumors.
作者 沈晓东
出处 《胃肠病学和肝病学杂志》 CAS 2013年第12期1234-1238,共5页 Chinese Journal of Gastroenterology and Hepatology
关键词 肠道肿瘤 ApcΔ716 +小鼠 DNA结合抑制物2 Intestinal neoplasms Id2 ApcΔ716/+mice Inhibitor of DNA binding 2
  • 相关文献

参考文献20

  • 1Dove WF,Clipson L,Gould KA. Intestinal neoplasia in the ApcMin mouse:independence from the microbial and natural killer (beige locus) status[J].Cancer Research,1997,(05):812-814.
  • 2Oshima M,Oshima H,Kitagawa K. Loss of Apc heterozygosity and abnormal tissue building in nascent intestinal polyps in mice carrying a truncated Apc gene[J].Proceedings of the National Academy of Sciences(USA),1995,(10):4482-4486.
  • 3房殿春,汪荣泉,杨仕明,杨建民,彭贵勇,肖天利.大肠癌APC基因15外显子突变分析[J].胃肠病学和肝病学杂志,2004,13(2):143-146. 被引量:9
  • 4Gumbiner BM. Propagation and localization of Wnt signaling[J].Current Opinion in Genetics and Development,1998,(04):430-435.doi:10.1016/S0959-437X(98)80114-7.
  • 5Pennisi E. How a growth control path takes a wrong turn to cancer[J].Science,1998,(5382):1438-1439,1441.
  • 6Ciznadija D,Tothill R,Waterman ML. Intestinal adenoma formation and MYC activation are regulated by cooperation between MYB and Wnt signaling[J].Cell Death and Differentiation,2009,(11):1530-1538.
  • 7Sikder HA,Devlin MK,Dunlap S. Id proteins in cell growth and tumorigenesis[J].Cancer Cells,2003,(06):525-530.
  • 8朱传东,李晓军.分化抑制因子与肿瘤相关性研究进展[J].生物化学与生物物理进展,2008,35(9):986-990. 被引量:10
  • 9高璐,卫立辛,吴孟超.分化抑制因子的表达与恶性肿瘤的预后[J].第二军医大学学报,2010,31(1):97-100. 被引量:4
  • 10李志雄,林杰成,林建生.Id蛋白与肿瘤及肿瘤性血管生成关系[J].现代肿瘤医学,2008,16(1):151-153. 被引量:7

二级参考文献128

  • 1李晓军,秦浚川.细胞分化抑制因子(Id)研究进展[J].生物化学与生物物理进展,2004,31(10):865-869. 被引量:29
  • 2李晓莉,赵艳滨,孙立春,李乐静.Id基因在多种肺癌细胞中的表达及意义[J].现代生物医学进展,2006,6(2):36-38. 被引量:9
  • 3雷婷,韩霜,郭雪艳,丁锐,李颖,谢华红,白飞虎,吴开春,丁杰.分化抑制因子1在环氧合酶2介导的胃癌血管生成中的作用及机制研究[J].中华医学杂志,2007,87(22):1570-1575. 被引量:12
  • 4贾海军,胡丽娜.细胞分化抑制因子Id与妇科肿瘤[J].现代妇产科进展,2007,16(5):386-387. 被引量:2
  • 5Norton J D. ID helix-loop-helix proteins in cell growth,differen tiation and tumorigenesis[J]. J Cell Sci, 2000,113 (Pt 22) : 3897-3905.
  • 6Ling M T,Wang X,Zhang X,Wong Y C. The multiple roles of Id-Ⅰ in cancer progression[J]. Differentiation, 2006,74 ( 9-10 ): 481-487.
  • 7Cummings S D, Ryu B, Samuels M A, Yu X, Meeker A K, Healey M A,et al. Idl delays senescence of primary human melanocytes[J]. Mol Carcinog, 2008,47 :653-659.
  • 8Norton J D,Atherton G T. Coupling of cell growth control and apoptosis functions of Id proteins[J]. Mol Cell Biol, 1998,18: 2371-2381.
  • 9Sikder H A,Devlin M K,Dunlap S,Ryu B, Alani R M. Id proteins in cell growth and tumorigenesis[J]. Cancer Cell, 2003,3:525-530.
  • 10Ko M,Ahn J,Lee C,Chung H,Jeon S H,Chung H Y, et al. E2A/HEB and Id3 proteins control the sensitivity to glucocorticoid induced apoptosis in thymocytes by regulating the SRG3 expression[J]. J Biol Chem,2004,279:21916-21923.

共引文献22

同被引文献10

引证文献1

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