Evidence map›Paper›PMID 32112420›Full record

ArticleHepatology (Baltimore, Md.)2020

Activation of Estrogen Receptor G Protein-Coupled Receptor 30 Enhances Cholesterol Cholelithogenesis in Female Mice.

Helen H Wang, Ornella de Bari, Christopher K Arnatt, Min Liu, Piero Portincasa, David Q-H Wang

Open access · greenAbstract read
In one paragraph

Article in Hepatology (Baltimore, Md.), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
1.5field-weighted citation impact, top 15% 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

30 citing papers in PubMed, 40 citations in OpenAlex.

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  18. Current Gallstone Treatment Methods, State of the Art.Diseases (Basel, Switzerland) · 2024
    Review
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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

6 authors at 4 institutions in 2 countries.

Helen H WangDepartment of Medicine and Genetics, Division of Gastroenterology and Liver Diseases, Marion Bessin Liver Research Center, Einstein-Mount Sinai Diabetes Research Center, Albert Einstein College of Medicine, Bronx, NY.
Ornella de BariDepartment of Internal Medicine, Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St. Louis, MO.
Christopher K ArnattDepartment of Chemistry, Saint Louis University, St. Louis, MO.
Min LiuDepartment of Pathology and Laboratory Medicine, University of Cincinnati College of Medicine, Cincinnati, OH.
Piero PortincasaDepartment of Biomedical Sciences and Human Oncology, Clinica Medica "A. Murri", University of Bari Medical School, Bari, Italy.
David Q-H WangDepartment of Medicine and Genetics, Division of Gastroenterology and Liver Diseases, Marion Bessin Liver Research Center, Einstein-Mount Sinai Diabetes Research Center, Albert Einstein College of Medicine, Bronx, NY.ORCID 0000-0002-5439-7651
Albert Einstein College of Medicine · USSaint Louis University · USUniversity of Bari Aldo Moro · ITUniversity of Cincinnati Medical Center · US

Funding

Special Animal CoreP30DK041296 · NIDDK · YESHIVA UNIVERSITY · PI GUPTA, SANJEEV · 1989 to 2018
$22.9M
GPR30 and hepatic cholesterol metabolismR01DK126369 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI PESSIN, JEFFREY E. · 2020 to 2023
$1.9M
Apolipoprotein A5 and Gallstone FormationR01DK114516 · NIDDK · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WANG, DAVID Q · 2018 to 2021
$1.5M
GPR30 and Hepatic Cholesterol HomeostasisR01DK106249 · NIDDK · SAINT LOUIS UNIVERSITY · PI WANG, DAVID Q · 2015 to 2017
$1.0M
Gene therapy of alcoholic liver diseaseR21AA025737 · NIAAA · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI WANG, DAVID Q · 2017 to 2018
$438k
Role of GPR30 in Hepatic Lipid MetabolismR56DK101793 · NIDDK · SAINT LOUIS UNIVERSITY · PI WANG, DAVID Q · 2014 to 2014
$189k
NIAAA NIH HHS AA025737NIAAA NIH HHS R21 AA025737NIDDK NIH HHS DK041296NIDDK NIH HHS DK101793NIDDK NIH HHS DK106249NIDDK NIH HHS DK114516NIDDK NIH HHS P30 DK041296NIDDK NIH HHS R01 DK106249NIDDK NIH HHS R01 DK114516NIDDK NIH HHS R01 DK126369NIDDK NIH HHS R56 DK101793
6 · The paper itself

Abstract

BACKGROUND AND

aimsEstrogen is an important risk factor for cholesterol gallstone disease because women are twice as likely as men to form gallstones. The classical estrogen receptor α (ERα), but not ERβ, in the liver plays a critical role in the formation of estrogen-induced gallstones in female mice. The molecular mechanisms underlying the lithogenic effect of estrogen on gallstone formation have become more complicated with the identification of G protein-coupled receptor 30 (GPR30), an estrogen receptor. APPROACH AND

resultsWe investigated the biliary and gallstone phenotypes in ovariectomized female GPR30

conclusionsGPR30 produces additional lithogenic actions, working independently of ERα, to increase susceptible to gallstone formation in female mice; both GPR30 and ERα are potential therapeutic targets for cholesterol gallstone disease, particularly in women and patients exposed to high levels of estrogen.

Indexed as

Estrogen Receptor alphaEstrogensGallstonesReceptors, EstrogenReceptors, G-Protein-CoupledAnimalsBileBile Acids and SaltsCholesterolCyclopentanesDisease Models, AnimalFemaleGallbladderHumansLipid MetabolismLiver1-(4-(6-bromobenzo(1,3)dioxol-5-yl)-3a,4,5,9b-tetrahydro-3H-cyclopenta(c)quinolin-8-yl)ethanoneBile Acids and SaltsCholesterolCyclopentanesEsr1 protein, mouseEstrogen Receptor alphaEstrogensGPER1 protein, mouseQuinolinesReceptors, EstrogenReceptors, G-Protein-Coupled

Identifiers

PMID32112420
PMCPMC8157628
OpenAlexW3008554522

What OpenQuestion holds

Textmetadata
LicenceTDM
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.