• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

他莫昔芬治疗乳腺癌后 GPR30 在子宫内膜病理中的作用。

Role of GPR30 in endometrial pathology after tamoxifen for breast cancer.

机构信息

Department of Obstetrics and Gynecology, Otto-von-Guericke University, Magdeburg, Germany.

出版信息

Am J Obstet Gynecol. 2010 Dec;203(6):595.e9-16. doi: 10.1016/j.ajog.2010.07.034. Epub 2010 Oct 20.

DOI:10.1016/j.ajog.2010.07.034
PMID:20965484
Abstract

OBJECTIVE

This study was undertaken to evaluate the potential role of G-protein-coupled estrogen receptor in endometrial pathology associated with tamoxifen treatment of breast cancer patients.

STUDY DESIGN

We investigated whether G-protein-coupled estrogen receptor plays a role in mediating proliferating effect of tamoxifen in endometrial carcinoma cells. These results were compared with the G-protein-coupled estrogen receptor expression pattern in endometrial tissue from a cohort of 95 breast cancer patients, who received tamoxifen or another adjuvant therapy.

RESULTS

In vitro tamoxifen significantly stimulated the mitogen-activated protein kinase phosphorylation and cell proliferation of endometrial cell lines via G-protein-coupled estrogen receptor. In vivo, there was a significant correlation between G-protein-coupled estrogen receptor expression and the tamoxifen-induced endometrial pathology (P = .006). Moreover, G-protein-coupled estrogen receptor positivity was predictive of an earlier development of symptoms, such as bleeding or suspect endometrial thickness, induced by tamoxifen therapy (P = .019).

CONCLUSION

G-protein-coupled estrogen receptor plays an important role in tamoxifen-induced endometrial abnormalities.

摘要

目的

本研究旨在评估 G 蛋白偶联雌激素受体在与乳腺癌患者接受他莫昔芬治疗相关的子宫内膜病理中的潜在作用。

研究设计

我们研究了 G 蛋白偶联雌激素受体是否在介导他莫昔芬对子宫内膜癌细胞的增殖作用中发挥作用。这些结果与 95 例接受他莫昔芬或其他辅助治疗的乳腺癌患者的子宫内膜组织中 G 蛋白偶联雌激素受体表达模式进行了比较。

结果

体外他莫昔芬通过 G 蛋白偶联雌激素受体显著刺激了子宫内膜细胞系的丝裂原激活蛋白激酶磷酸化和细胞增殖。体内,G 蛋白偶联雌激素受体的表达与他莫昔芬引起的子宫内膜病变之间存在显著相关性(P =.006)。此外,G 蛋白偶联雌激素受体阳性预测了他莫昔芬治疗引起的症状(如出血或可疑的子宫内膜增厚)更早出现(P =.019)。

结论

G 蛋白偶联雌激素受体在他莫昔芬诱导的子宫内膜异常中发挥重要作用。

相似文献

1
Role of GPR30 in endometrial pathology after tamoxifen for breast cancer.他莫昔芬治疗乳腺癌后 GPR30 在子宫内膜病理中的作用。
Am J Obstet Gynecol. 2010 Dec;203(6):595.e9-16. doi: 10.1016/j.ajog.2010.07.034. Epub 2010 Oct 20.
2
[Histological analysis of endometrial polyps in breast cancer patients treated with tamoxifen (nolvadex)].[他莫昔芬(诺瓦得士)治疗的乳腺癌患者子宫内膜息肉的组织学分析]
Akush Ginekol (Sofiia). 2004;43(2):33-6.
3
[Postmenopausal hemorrhage and endometrial cancer in tamoxifen therapy].[他莫昔芬治疗中的绝经后出血与子宫内膜癌]
Zentralbl Gynakol. 1994;116(1):44-7.
4
Tamoxifen and endometrial cancer.他莫昔芬与子宫内膜癌。
Mt Sinai J Med. 1992 Oct;59(5):416-8.
5
The nature of tamoxifen action in the control of female breast cancer.他莫昔芬在女性乳腺癌控制中的作用本质。
In Vivo. 2001 Jul-Aug;15(4):319-25.
6
Outcomes in patients with primary breast cancer and a subsequent diagnosis of endometrial cancer : comparison of cohorts treated with and without tamoxifen.原发性乳腺癌患者随后被诊断为子宫内膜癌的结局:接受他莫昔芬治疗与未接受他莫昔芬治疗队列的比较。
Cancer. 2007 Jul 1;110(1):31-7. doi: 10.1002/cncr.22734.
7
A clinicopathologic study on patients with endometrial cancer after adjuvant tamoxifen treatment for breast cancer: a single center experience.一项关于乳腺癌辅助他莫昔芬治疗后发生子宫内膜癌患者的临床病理研究:单中心经验
Breast J. 2006 Nov-Dec;12(6):578-84. doi: 10.1111/j.1524-4741.2006.00353.x.
8
Tamoxifen treatment for breast cancer and risk of endometrial cancer: a case-control study.他莫昔芬治疗乳腺癌与子宫内膜癌风险:一项病例对照研究。
J Natl Cancer Inst. 2005 Mar 2;97(5):375-84. doi: 10.1093/jnci/dji057.
9
Estrogen and progesterone receptor expression in postmenopausal tamoxifen-exposed endometrial pathologies.绝经后接受他莫昔芬治疗的子宫内膜病变中雌激素和孕激素受体的表达
Gynecol Oncol. 1997 Oct;67(1):8-15. doi: 10.1006/gyno.1997.4831.
10
Endometrial histopathology in 700 patients treated with tamoxifen for breast cancer.700例接受他莫昔芬治疗的乳腺癌患者的子宫内膜组织病理学情况。
Gynecol Oncol. 2000 Aug;78(2):181-6. doi: 10.1006/gyno.2000.5859.

引用本文的文献

1
Unveiling the Pathogenesis of Adenomyosis through Animal Models.通过动物模型揭示子宫腺肌病的发病机制。
J Clin Med. 2022 Mar 21;11(6):1744. doi: 10.3390/jcm11061744.
2
Estrogen Receptor Function: Impact on the Human Endometrium.雌激素受体功能:对人子宫内膜的影响。
Front Endocrinol (Lausanne). 2022 Feb 28;13:827724. doi: 10.3389/fendo.2022.827724. eCollection 2022.
3
The impact of G protein-coupled oestrogen receptor 1 on male breast cancer: a retrospective analysis.G蛋白偶联雌激素受体1对男性乳腺癌的影响:一项回顾性分析。
Contemp Oncol (Pozn). 2021;25(3):204-212. doi: 10.5114/wo.2021.110010. Epub 2021 Oct 14.
4
Tamoxifen and Endometrial Cancer: A Janus-Headed Drug.他莫昔芬与子宫内膜癌:一种双面性药物。
Cancers (Basel). 2020 Sep 7;12(9):2535. doi: 10.3390/cancers12092535.
5
Endocrine Risk Factors of Endometrial Cancer: Polycystic Ovary Syndrome, Oral Contraceptives, Infertility, Tamoxifen.子宫内膜癌的内分泌危险因素:多囊卵巢综合征、口服避孕药、不孕症、他莫昔芬。
Cancers (Basel). 2020 Jul 2;12(7):1766. doi: 10.3390/cancers12071766.
6
G-Protein Coupled Estrogen Receptor in Breast Cancer.G 蛋白偶联雌激素受体在乳腺癌中的作用。
Int J Mol Sci. 2019 Jan 14;20(2):306. doi: 10.3390/ijms20020306.
7
GPCR Modulation in Breast Cancer.G 蛋白偶联受体在乳腺癌中的调节作用。
Int J Mol Sci. 2018 Dec 2;19(12):3840. doi: 10.3390/ijms19123840.
8
International Union of Basic and Clinical Pharmacology. XCVII. G Protein-Coupled Estrogen Receptor and Its Pharmacologic Modulators.国际基础与临床药理学联合会。XCVII。G蛋白偶联雌激素受体及其药理学调节剂。
Pharmacol Rev. 2015 Jul;67(3):505-40. doi: 10.1124/pr.114.009712.
9
Molecular mechanisms of tamoxifen-associated endometrial cancer (Review).他莫昔芬相关子宫内膜癌的分子机制(综述)
Oncol Lett. 2015 Apr;9(4):1495-1501. doi: 10.3892/ol.2015.2962. Epub 2015 Feb 12.
10
Estrogen receptor alpha prevents bladder cancer via INPP4B inhibited akt pathway in vitro and in vivo.雌激素受体α通过抑制INPP4B的Akt信号通路在体内外预防膀胱癌。
Oncotarget. 2014 Sep 15;5(17):7917-35. doi: 10.18632/oncotarget.1421.