Evidence map›Paper›PMID 26977530›Full record

ArticleThe Journal of clinical endocrinology and metabolism2016

Activated Hippo/Yes-Associated Protein Pathway Promotes Cell Proliferation and Anti-apoptosis in Endometrial Stromal Cells of Endometriosis.

Yong Song, Jing Fu, Min Zhou, Li Xiao, Xue Feng, Hengxi Chen, Wei Huang

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
4.4field-weighted citation impact, top 6% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 102 citations in OpenAlex.

  1. Pooled it
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  11. The SOX18-OTUB1-YAP1 axis: a new endometriosis target.Journal of translational medicine · 2025
    Article
  12. Hippo signaling in mammalian reproduction.Reproduction (Cambridge, England) · 2025
    Review
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3 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 2 institutions in 1 country.

Yong SongDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
Jing FuDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
Min ZhouDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
Li XiaoDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
Xue FengDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
Hengxi ChenDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
Wei HuangDepartment of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu Sichuan 610041, People's Republic of China.
West China Second University Hospital of Sichuan University · CNSichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextThe imbalance in cell proliferation and apoptosis is considered an important role in the pathogenesis of endometriosis, but the exact mechanisms remains unclear. A newly established signaling pathway–Hippo/Yes-associated protein (YAP) pathway plays a critical role in the proliferation and apoptosis processes. However, studies focusing on Hippo/YAP pathway and endometriosis are lacking.

objectiveThe objective was to explore the function of the Hippo/YAP pathway in endometriosis. SETTING AND

designThe expression of YAP was first investigated in endometrium of women with or without endometriosis. The role of YAP in cell proliferation and apoptosis is identified by transfection of endometrial stromal cells (ESCs) in vitro, subsequent Verteporfin treatments in eutopic ESCs in vitro, and endometriosis animal model of nude mice in vivo.

resultsOur results revealed that increased expression of YAP and decreased expression of p-YAP in ectopic and eutopic endometrium compared with normal endometrium. YAP knockdown in eutopic ESCs decreased cell proliferation and enhanced cell apoptosis companied with decreased expression of TEAD1, CTGF, and B-cell lymphoma/leukemia (BCL)-2; whereas overexpression of YAP resulted in increased proliferation and decreased apoptosis of normal ESCs with increased expression of TEAD1, CTGF, and BCL-2. By chromatin immunoprecipitation qPCR CTGF and BCL-2 were identified as directly downstream target genes of YAP-TEAD1 active complex. Eutopic ESCs treated with Verteporfin revealed decreased proliferation and enhanced apoptosis whereas in endometriosis animal models of nude mice treated with Verteporfin, the size of endometriotic lesions was significantly reduced.

conclusionsOur study suggests that the Hippo/YAP-signaling pathway plays a critical role in the pathogenesis of endometriosis and should present a novel therapeutic method against endometriosis.

Indexed as

ApoptosisCell ProliferationAdultAnimalsBlotting, WesternEndometriosisEndometriumFemaleFlow CytometryHippo Signaling PathwayHumansImmunoenzyme TechniquesMiceMice, Inbred BALB CMice, NudeProtein Serine-Threonine KinasesProtein Serine-Threonine KinasesProto-Oncogene Proteins c-yesRNA, MessengerYES1 protein, human

Identifiers

PMID26977530
PMCPMC4880175
OpenAlexW2301845119

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.