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神经细胞黏附因子在子宫腺肌病病灶中的表达及意义

石茜茜 李辉 秦晓燕 王芳 温泽清 李长忠 王飞

现代妇产科进展Issue(6):408-411,4.
现代妇产科进展Issue(6):408-411,4.DOI:10.13283/j.cnki.xdfckjz.2015.06.003

神经细胞黏附因子在子宫腺肌病病灶中的表达及意义

Expression and significance of neural cell adhesion molecule in adenomyosis

石茜茜 1李辉 1秦晓燕 1王芳 1温泽清 1李长忠 1王飞1

作者信息

  • 1. 山东大学附属省立医院妇科,济南 250021
  • 折叠

摘要

Abstract

Objective:To investigate the expression of neural cell adhesion molecule ( NCAM) in the eutopic endometrium and ectopic lesions from patients in adenomyosis and its possible role in the pethogenesis of adenomyosis. Methods:The expressions of NCAM in the eu-topic and ectopic samples of adenomyosis were assayed by immunohistochemical staining and the result was compared with the normal endometrial samples by H-score method. Result:NCAM was observed in the endometrial glandular epithelium of all the ectopic and ectopic sam-ples and 19 normal samples. No positive results were observed in stroma. The staining intensity of NCAM in ectopic lesion was significantly higher than that in the eutopic endometrium and normal endometrium ( P<0 . 01 ) , whereas no statistical difference was observed in the expres-sion between the eutopic endometrium and normal endometrium of patients with adenomyosis. For eutopic endometrium of adenomyosis,expression was higher in the secretory phase than that in the proliferative phase(P<0. 05). The expression of NCAM in ectopic lesion of adenomyosis was positively correlated with the severity of dysmenorrhea ( r=0 . 84 , P<0 . 01 ) . Conclusions:NCAM may participate in the occurrence and development of adenomyosis and may contributes to the occurrence and development of dymenorrhea,but the exact moleculor mechanisms still re-main to be discovered.

关键词

NCAM/子宫腺肌病/子宫内膜/免疫组化

Key words

NCAM/Adenomyosis/Endometrium/Immunohistochemistry

分类

医药卫生

引用本文复制引用

石茜茜,李辉,秦晓燕,王芳,温泽清,李长忠,王飞..神经细胞黏附因子在子宫腺肌病病灶中的表达及意义[J].现代妇产科进展,2015,(6):408-411,4.

基金项目

国家自然科学基金资助项目(No:81200426);山东省自然科学基金资助项目(No. ZR2013HM060;No:ZR2011HQ046);山东省科技发展计划(No:2014GSF118048) (No:81200426)

现代妇产科进展

OA北大核心CSCDCSTPCD

1004-7379

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