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CXCL14在子宫内膜异位症增生期内膜中的表达
引用本文:邹阮敏,林刻智,余霞,余剑琴,阮静瑶,陈冠阁,张文淼. CXCL14在子宫内膜异位症增生期内膜中的表达[J]. 温州医科大学学报, 2016, 46(6): 422-426
作者姓名:邹阮敏  林刻智  余霞  余剑琴  阮静瑶  陈冠阁  张文淼
作者单位:1.温州医科大学附属第一医院妇产科,浙江温州325015;2.温州医科大学基础医学实验中心,浙江温州325035;3.温州医科大学附属第一医院病理科,浙江温州325015
基金项目:温州市科技局科研基金资助项目(Y20140308,Y2014 0216);浙江省自然科学青年基金资助项目(LQ15C010002)。
摘    要:目的:分析CXCL14在子宫内膜异位症增生期在位内膜及异位内膜中的表达情况。方法:采取Real-time PCR和免疫组织化学染色法对手术和病理确诊增生期子宫内膜异位症的18例在位内膜、24例异位内膜及20例因行卵巢囊肿、子宫肌瘤手术的增生期正常子宫内膜(术后病理除外子宫内膜异位症)进行CXCL14表达的检测。结果:①与正常内膜比较,III-IV期子宫内膜异位症在位内膜的CXCL14 mRNA和蛋白表达水平明显下调,差异有统计学意义(P<0.05);②与正常内膜比较,I-II期子宫内膜异位症在位内膜的CXCL14 mRNA和蛋白表达水平有下调,但差异无统计学意义(P>0.05);③与III-IV期子宫内膜异位症在位内膜比较,III-IV期子宫内膜异位症异位内膜的CXCL14 mRNA和蛋白表达水平明显下调,差异有统计学意义(P<0.05);与I-II期在位内膜比较,I-II期异位内膜的CXCL14 mRNA和蛋白表达水平有下调,但差异无统计学意义(P>0.05)。结论:CXCL14可能参与子宫内膜异位症的发生、发展,可能与子宫内膜异位症患者妊娠率低有关。

关 键 词:CXCL14  子宫内膜异位症  正常内膜  在位内膜  异位内膜
  
收稿时间:2016-01-20

Expression of chemokine CXCL14 in the proliferative-phase endometriosis
ZOU Ruanmin,LIN Kezhi,YU Xia,YU Jianqin,RUAN Jingyao,CHEN Guan’ge,ZHANG Wenmiao.. Expression of chemokine CXCL14 in the proliferative-phase endometriosis[J]. JOURNAL OF WENZHOU MEDICAL UNIVERSITY, 2016, 46(6): 422-426
Authors:ZOU Ruanmin  LIN Kezhi  YU Xia  YU Jianqin  RUAN Jingyao  CHEN Guan’ge  ZHANG Wenmiao.
Affiliation:1.Department of Obstetrics and Gynecology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015; 2.Medical Experimental Teaching Center, Wenzhou Medical University, Wenzhou, 325035; 3.Department of Pathology, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325015;
Abstract:Objective: To analyze the expression of chemokine CXCL14 in the eutopic and ectopic endometrium of the proliferative-phase endometriosis. Methods: Real-time PCR and immunohistochemistry were adopted to measure and compare the CXCL14 expression in 18 cases of eutopic endometrium, 24 cases of ectopic endometrium and 20 cases of normal endometrium, which were confirmed by surgery and pathology. Results: ①Compared to normal endometrium, the expression of chemokine CXCL14 at mRNA and protein levels significantly declined in eutopic endometrium with stage III-IV, there were significant differences (P<0.05). ②Compared to normal endometrium, the expression of chemokine CXCL14 at mRNA and protein levels declined slightly in eutopic endometrium with stage I-II, but there were no significant differences. ③The chemokine CXCL14 at mRNA and protein levels were significantly down-regulated in ectopic endometrium with stage III-IV compared to eutopic endometrium with stage III-IV (P<0.05). ④The chemokine CXCL14 at mRNA and protein levels were slightly down-regulated in ectopic endometrium with stage I-II compared to eutopic endometrium with stage I-II. Conclusion: Our findings indicated that CXCL14 may participate in the development and progression of endometriosis, which is likely associated with the low conception rates in women with endometriosis.
Keywords:CXCL14  endometriosis  normal endometrium  eutopic endometrium  ectopic endometrium  
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