Evidence map›Paper›PMID 32127396›Full record

ArticleJournal of lipid research2020

A novel GPER antagonist protects against the formation of estrogen-induced cholesterol gallstones in female mice.

Chelsea DeLeon, Helen H Wang, Joseph Gunn, McKenna Wilhelm, Aidan Cole, Stacy Arnett, David Q-H Wang, Christopher K Arnatt

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

18 citing papers in PubMed, 26 citations in OpenAlex.

  1. Article
  2. Alkamines reveal a hidden layer of steroid and drug metabolism.bioRxiv : the preprint server for biology · 2026
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  17. GPER and Testicular Germ Cell Cancer.Frontiers in endocrinology · 2020
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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

8 authors at 2 institutions in 1 country.

Chelsea DeLeonDepartment of ChemistrySaint Louis University, St. Louis, MO.
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.
Joseph GunnDepartment of ChemistrySaint Louis University, St. Louis, MO.
McKenna WilhelmDepartment of ChemistrySaint Louis University, St. Louis, MO.
Aidan ColeDepartment of ChemistrySaint Louis University, St. Louis, MO.
Stacy ArnettCenter for World Health and Medicine,Saint Louis University, St. Louis, MO.
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. Electronic address: mailto:chris.arnatt@slu.edu.
Christopher K ArnattDepartment of ChemistrySaint Louis University, St. Louis, MO.
Saint Louis University · USAlbert Einstein College of Medicine · 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 R21 AA025737NIDDK 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

Many clinical studies and epidemiological investigations have clearly demonstrated that women are twice as likely to develop cholesterol gallstones as men, and oral contraceptives and other estrogen therapies dramatically increase that risk. Further, animal studies have revealed that estrogen promotes cholesterol gallstone formation through the estrogen receptor (ER) α, but not ERβ, pathway. More importantly, some genetic and pathophysiological studies have found that G protein-coupled estrogen receptor (GPER) 1 is a new gallstone gene,

Indexed as

AnimalsCalciumCholesterolCyclic AMPEstrogensFemaleGallstonesHL-60 CellsHumansMiceReceptors, EstrogenReceptors, G-Protein-CoupledSignal TransductionCalciumCholesterolCyclic AMPEstrogensGPER1 protein, mouseReceptors, EstrogenReceptors, G-Protein-Coupledbilebile saltscrystallizationG protein-coupled estrogen receptorLithmucin

Identifiers

PMID32127396
PMCPMC7193967
OpenAlexW3010488216

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.