Evidence map›Paper›PMID 33706098›Full record

ArticleBiochemical and biophysical research communications2021

ARID1A and PGR proteins interact in the endometrium and reveal a positive correlation in endometriosis.

Hong Im Kim, Tae Hoon Kim, Jung-Yoon Yoo, Steven L Young, Bruce A Lessey, Bon Jeong Ku, Jae-Wook Jeong

Open access · greenAbstract read
In one paragraph

Article in Biochemical and biophysical research communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
3.1field-weighted citation impact, top 9% 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

15 citing papers in PubMed, 22 citations in OpenAlex.

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  8. The roles of chromatin regulatory factors in endometriosis.Journal of assisted reproduction and genetics · 2024
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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 5 institutions in 3 countries.

Hong Im KimDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, Grand Rapids, MI, 49503, USA.
Tae Hoon KimDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, Grand Rapids, MI, 49503, USA.
Jung-Yoon YooDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, Grand Rapids, MI, 49503, USA; Life Science Institute, Repure Life Science, Seoul, 03722, Republic of Korea.
Steven L YoungDepartment of Obstetrics and Gynecology, University of North Carolina, Chapel Hill, NC, 27514, USA.
Bruce A LesseyDepartment of Obstetrics and Gynecology, Wake Forest Baptist Health, Winston-Salem, NC, 27157, USA.
Bon Jeong KuDepartment of Internal Medicine, Chungnam National University College of Medicine, Daejeon, 35015, Republic of Korea. Electronic address: bonjeong@cnu.ac.kr.
Jae-Wook JeongDepartment of Obstetrics, Gynecology and Reproductive Biology, Michigan State University, Grand Rapids, MI, 49503, USA. Electronic address: jeongj@msu.edu.
Michigan State University · USAtrium Health Wake Forest Baptist · USChungnam National University · KRLife Science Institute · JPUniversity of North Carolina at Chapel Hill · US

Funding

Molecular mechanisms of endometrial progesterone resistanceR01HD101243 · NICHD · UNIVERSITY OF MISSOURI-COLUMBIA · PI JEONG, JAE-WOOK · 2020 to 2024
$2.6M
Risk factors for early pregnancy lossR01HD084478 · NICHD · MICHIGAN STATE UNIVERSITY · PI JEONG, JAE-WOOK · 2016 to 2020
$1.6M
NICHD NIH HHS R01 HD084478NICHD NIH HHS R01 HD101243
6 · The paper itself

Abstract

Endometriosis is a disorder in which endometrial cells normally limited to the lining of the uterus proliferate outside the uterine cavity and can cause pelvic pain and infertility. ARID1A levels are significantly reduced in the eutopic endometrium from women with endometriosis. Uterine specific Arid1a knock-out mice were infertile due to loss of epithelial progesterone receptor (PGR) signaling. However, the functional association of ARID1A and PGR in endometriosis has not been studied. We examined the expression patterns and co-localization of ARID1A and PGR in eutopic endometrium from women with and without endometriosis using immunostaining and Western blot analysis. ARID1A and PGR proteins co-localized in the epithelium during the proliferative and the early secretory phases. Our immunoprecipitation analysis and proximity ligation assay (PLA) revealed physical interaction between ARID1A and PGR-A but not PGR-B in the mouse and human endometrium. ARID1A levels positively correlated with PGR levels in the eutopic endometrium of women with endometriosis. Our results bring new perspectives on the molecular mechanisms involved in endometrial receptivity and progesterone resistance in endometriosis. The interrelationship between ARID1A and PGR may contribute to explaining the non-receptive endometrium in endometriosis-related infertility.

Indexed as

AnimalsDNA-Binding ProteinsEndometriosisEndometriumFemaleHEK293 CellsHumansImmunoprecipitationMiceProtein BindingReceptors, ProgesteroneTranscription FactorsARID1A protein, humanArid1a protein, mouseDNA-Binding ProteinsReceptors, ProgesteroneTranscription FactorsARID1AEndometriosisEndometriumProgesterone receptor

Identifiers

PMID33706098
PMCPMC8005488
OpenAlexW3134343606

What OpenQuestion holds

Textmetadata
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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.