YAP1 inhibits ovarian endometriosis stromal cell invasion through ESR2

转染 雅普1 子宫内膜异位症 雌激素受体 间质细胞 癌症研究 蜕膜化 化学 医学 生物 细胞生物学 内分泌学 内科学 转录因子 细胞培养 基因 癌症 乳腺癌 遗传学 生物化学
作者
Cheng Zeng,Peili Wu,Zhao-tong Dong,Xin Li,Yingfang Zhou,Qing Xue
出处
期刊:Reproduction [Bioscientifica]
卷期号:160 (3): 481-490 被引量:4
标识
DOI:10.1530/rep-19-0565
摘要

Endometriosis is an estrogen-dependent disease, and estrogen receptor 2 ( ESR2 ) plays a critical role in the pathogenesis of ovarian endometriosis by promoting cell invasion. Yes-associated protein 1 ( YAP1 ) plays suppressive roles in several types of tumors. However, the relationship between YAP1 and ESR2 is not fully understood. The aim of this study was to investigate the regulatory mechanism of YAP1 in terms of ESR2 and YAP1 regulation of endometriotic stromal cell (ECSC) invasion in ovarian endometriosis. Our results demonstrated that YAP1 mRNA and protein levels in eutopic endometrium (EU) tissues were higher than those in paired ectopic endometrium (EC) tissues. ECSCs transfected with siYAP1 exhibited a significant increase in both ESR2 mRNA levels and protein expression. Simultaneously, YAP1 overexpression in ECSCs yielded the opposite results. Co-IP assays demonstrated YAP1-NuRD complex formation by YAP1, CHD4 and MTA1 in ECSCs. YAP1 bound to two sites, (-539, -533) and (-158, -152), upstream of the ESR2 transcription initiation site. YAP1 binding to the two sites of the ESR2 promoter in ECSCs was significantly lower than that in eutopic endometrial stromal cells (EUSCs) from EU tissues. ECSCs transfected with siYAP1 exhibited increased invasion activity, while ECSCs transfected with siESR2 showed inhibition of invasion. However, transfection with siYAP1 and siESR2 together decreased the number of invading cells compared with transfection with siYAP1 alone. Therefore, we conclude that decreased levels of YAP1 in ovarian endometriomas enhance ESR2 expression via formation of a YAP1-NuRD complex, which further binds to the ESR2 promoters. Furthermore, YAP1 inhibits ECSCs invasion.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
852应助旺旺雪饼采纳,获得10
1秒前
1秒前
1秒前
慕青应助ned采纳,获得10
1秒前
蒸镀金银回收应助skbkbe采纳,获得10
2秒前
搜集达人应助yy采纳,获得10
3秒前
4秒前
AKKKK发布了新的文献求助10
5秒前
郭团团完成签到,获得积分20
5秒前
木香007完成签到,获得积分10
6秒前
我是老大应助害羞的诺言采纳,获得10
7秒前
王木木发布了新的文献求助10
7秒前
7秒前
10秒前
Lucas应助一二采纳,获得10
11秒前
白鹿给友好冷之的求助进行了留言
13秒前
14秒前
14秒前
研友_nxGyxL发布了新的文献求助10
14秒前
xiaowang发布了新的文献求助10
15秒前
18秒前
18秒前
20秒前
wanci应助徐大夫采纳,获得10
20秒前
搜集达人应助Makho采纳,获得10
22秒前
旺旺雪饼发布了新的文献求助10
23秒前
橄榄汁柠檬茶完成签到,获得积分20
24秒前
研友_nxGyxL完成签到,获得积分10
24秒前
AKKKK完成签到,获得积分20
27秒前
科研通AI2S应助eritinn采纳,获得10
30秒前
31秒前
32秒前
传奇3应助木香007采纳,获得10
33秒前
11发布了新的文献求助10
34秒前
旺旺雪饼发布了新的文献求助10
37秒前
physics发布了新的文献求助10
39秒前
欢喜的南烟完成签到 ,获得积分10
43秒前
44秒前
45秒前
physics完成签到,获得积分10
45秒前
高分求助中
Manual of Clinical Microbiology, 4 Volume Set (ASM Books) 13th Edition 1000
Cross-Cultural Psychology: Critical Thinking and Contemporary Applications (8th edition) 800
Counseling With Immigrants, Refugees, and Their Families From Social Justice Perspectives pages 800
マンネンタケ科植物由来メロテルペノイド類の網羅的全合成/Collective Synthesis of Meroterpenoids Derived from Ganoderma Family 500
[Lambert-Eaton syndrome without calcium channel autoantibodies] 400
Statistical Procedures for the Medical Device Industry 400
藍からはじまる蛍光性トリプタンスリン研究 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 有机化学 工程类 生物化学 纳米技术 物理 内科学 计算机科学 化学工程 复合材料 遗传学 基因 物理化学 催化作用 电极 光电子学 量子力学
热门帖子
关注 科研通微信公众号,转发送积分 2376185
求助须知:如何正确求助?哪些是违规求助? 2084209
关于积分的说明 5227147
捐赠科研通 1810979
什么是DOI,文献DOI怎么找? 903888
版权声明 558463
科研通“疑难数据库(出版商)”最低求助积分说明 482527