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G 蛋白偶联受体 GPR30 的表达状态与子宫内膜异位症的临床特征有关。

The expression status of G protein-coupled receptor GPR30 is associated with the clinical characteristics of endometriosis.

机构信息

Department of Obstetrics and Gynecology, Osaka Medical College , Takatsuki, Osaka , Japan.

出版信息

Endocr Res. 2013;38(4):223-31. doi: 10.3109/07435800.2013.774011. Epub 2013 Mar 4.

Abstract

INTRODUCTION

GPR30 is a seven-transmembrane G protein-coupled estrogen receptor that regulates endometrial cellular responses to estrogen. GPR30 is often highly expressed in cancer cells from aggressive tumors. The aim of this study was to evaluate the expression patterns of GPR30 in endometriosis during medical treatment.

PATIENTS

A total of 38 females, 28 patients with endometriosis and 10 patients with leiomyoma who underwent laparoscopic surgery were included this study.

INTERVENTION

Eutopic endometrial tissue sampling from women without endometriosis and ectopic endometrial tissue sampling from women with endometriosis.

MAIN OUTCOME MEASURE

A quantitative real-time polymerase chain reaction analysis of the mRNA expression in eutopic and ectopic endometrial tissues with or without GnRH agonist treatment. The expression of GPR30 was confirmed by immunohistochemistry.

RESULTS

There was an increased level of GPR30 mRNA in eutopic endometrium during the proliferative phase, whereas higher expression was observed in the ectopic endometrium during the secretory phase. Increased GPR30 mRNA was observed in ectopic endometrium in comparison to eutopic endometrium. GnRH agonist treatment before laparoscopic surgery decreased GPR30 mRNA in ectopic endometrium. The immunohistochemical analysis also revealed that GPR30 was strongly expressed in epithelial cells in ectopic endometrium, whereas GnRH agonist treatment decreased the GPR30 expression.

CONCLUSION

High levels of GPR30 expression can play an important role in the progression of endometriosis.

摘要

简介

GPR30 是一种七跨膜 G 蛋白偶联雌激素受体,可调节子宫内膜细胞对雌激素的反应。GPR30 在侵袭性肿瘤的癌细胞中通常高度表达。本研究旨在评估 GPR30 在子宫内膜异位症治疗过程中的表达模式。

患者

共纳入 38 名女性,其中 28 名子宫内膜异位症患者和 10 名子宫肌瘤患者接受腹腔镜手术。

干预措施

从无子宫内膜异位症的女性中采集在位子宫内膜组织,从有子宫内膜异位症的女性中采集异位子宫内膜组织。

主要观察指标

用 GnRH 激动剂治疗或不治疗时,在位和异位子宫内膜组织中 mRNA 表达的定量实时聚合酶链反应分析。用免疫组织化学法确认 GPR30 的表达。

结果

增殖期在位子宫内膜中 GPR30 mRNA 水平升高,而分泌期异位子宫内膜中表达更高。与在位子宫内膜相比,异位子宫内膜中 GPR30 mRNA 表达增加。腹腔镜手术前 GnRH 激动剂治疗可降低异位子宫内膜中 GPR30 mRNA。免疫组织化学分析还显示,GPR30 在异位子宫内膜的上皮细胞中强烈表达,而 GnRH 激动剂治疗可降低 GPR30 表达。

结论

高水平的 GPR30 表达可能在子宫内膜异位症的进展中起重要作用。

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