期刊文献+

FOXP3与TGF-β1在卵巢异位子宫内膜中的表达及意义 被引量:1

Expression and significance of FOXP3 and TGF-β1 in ovarian endometriotic tissues
下载PDF
导出
摘要 目的探讨FOXP3和TGF-β1在卵巢异位内膜组织中的表达相关性及意义。方法采用免疫组织化学方法,检测40例卵巢异位子宫内膜、40例正常在位子宫内膜及40例正常卵巢组织中FOXP3和TGF-β1的表达情况及相关性。结果FOXP3在卵巢异位内膜组织中高表达,显著高于正常在位内膜(χ~2=22.55,P=0.000)及正常卵巢组织(χ~2=14.70,P=0.000);TGF-β1在卵巢异位内膜组织中多呈中度阳性、强阳性表达,显著高于正常在位内膜(χ~2=8.12,P=0.010)及正常卵巢组织(χ~2=4.34,P=0.037);FOXP3、TGF-β1在卵巢异位内膜组织中的表达具有正相关性(r=0.667,P=0.001)。结论卵巢异位内膜组织中,FOXP3、TGF-β1高表达且呈正相关,在两者的共同作用下,免疫状态被抑制,从而促进了内异症的发生及发展。 Objective To explore the expression and significance of FOXP3 and TGF-β1 expression in ovarian endometriotic tissues.Methods FOXP3 and TGF-β1 expression was detected in 40 cases of ovarian endometriotic tissues, 40 cases of normal endometrium tissues and 40 cases of normal ovarian tissues by immunohistochemistry(IHC), and their relationship was investigated.Results FOXP3 showed high expression in ovarian endometriotic tissues, significantly higher than that of normal endometrium tissues( χ 2 = 22.55 , P =0.000) and normal ovarian tissues( χ 2 =14.70, P =0.000). TGF-β1 showed moderate or strong positive expression in ovarian endometriotic tissues, and the expression was significantly higher than that in normal endometrium tissues( χ 2 =8.12, P = 0.010 ) and normal ovarian tissues( χ 2 =4.34, P =0.037). Spearman correlation analysis showed that the expression of FOXP3 was positively correlated with the expression of TGF-β1 in ovarian endometriotic tissues( r =0.667, P =0.001).Conclusion The expression of FOXP3 and TGF-β1 in ovarian endometriotic specimen is high and shows positive correlation, suggesting that they have synergistic effect in the occurrence and development of EMS.
作者 赵娟 樊晓慧 韩晓兵 ZHAO Juan;FAN Xiaohui;HAN Xiaobing(Department of Gynaecology and Obstetrics,First Affiliated Hospital of Xi'an Jiaotong University,Xi'an 710061,China)
出处 《山西医科大学学报》 CAS 2018年第6期614-617,共4页 Journal of Shanxi Medical University
关键词 子宫内膜异位症 FOXP3 TGF-Β1 endometriosis FOXP3 TGF-β1
  • 相关文献

参考文献8

二级参考文献59

  • 1Marie-Louise Ward,David J Crossman.Mechanisms underlying the impaired contractility of diabetic cardiomyopathy[J].World Journal of Cardiology,2014,6(7):577-584. 被引量:13
  • 2饶恩于,赵勇.调节性T细胞发育的一个关键转录因子Foxp3[J].生物化学与生物物理进展,2005,32(2):106-110. 被引量:6
  • 3杨晓鲲,郑峻松,张新,蒲晓允.GITR抗体介导增强NK细胞杀伤活性的实验研究[J].重庆医学,2006,35(18):1649-1651. 被引量:2
  • 4曾冬竹,余佩武,雷晓,石彦,王自强,郑峻松.CD4^+ CD25^+调控T细胞对小鼠胃癌的影响[J].中华胃肠外科杂志,2007,10(4):368-371. 被引量:7
  • 5Sakaguchi S,Sakaguchi N. Regulatory T cells in immunologic self tolerance and autoimmune disease[J]. Int Rev Immunol, 2005,24 ( 3- 4 ) : 211.
  • 6Beyer M, Schultze JL. Regulatory T cells in cancer[J]. Blood,2006,108(3) :804.
  • 7Ohmura Y,Yoshikawa K,Saga S, et al. Combinations of tumoPspecific CD8+ CTLs and anti-CD25 mAb provide improved immunolherapy[J]. Oncol Rep, 2008, 19(5): 1265.
  • 8Zaccone P, Burton O, Miller N, et al. Schistosoma manso ni egg antigens induce Treg that participate in diabetes prevention in NOD mice[J]. Eur J Immunol,2009,39(4) :1098.
  • 9Nishikawa H, Kato T, Tawara I, et al. Accelerated chemi cally induced tumor development mediated by CD4+ CD25+ regulatory T cells in wild type hosts[J]. Proc Natl Acad Sci USA,2005,102(26) :9253.
  • 10Thornton AM,Piccirillo CA,Shevach EM. ActiVation requirements for the induction of CD4+CD25+T cell sup pressor function[J]. Eur J Immunol, 2004,34 (2) : 366.

共引文献47

同被引文献3

引证文献1

二级引证文献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