Evidence map›Paper›PMID 39507056›Full record

ArticleFrontiers in endocrinology2024

Activation of estrogen-related receptor γ by calcium and cadmium.

Qiaochu Wang, Nanxi Huang, John B Psaltis, Reem M Gahtani, Gai Yan, Dajun Lu, Shannon R Cahalan, Xu Shi, Robert L Copeland, Bassem R Haddad and 1 more

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Association of urinary cadmium and arsenic with gynecological cancers: Results from NHANES 2003-2018.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Article
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

11 authors.

Qiaochu WangDepartment of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, United States.
Nanxi HuangOncology, Georgetown University, Washington DC, United States.
John B PsaltisOncology, Georgetown University, Washington DC, United States.
Reem M GahtaniDepartment of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, United States.
Gai YanOncology, Georgetown University, Washington DC, United States.
Dajun LuOncology, Georgetown University, Washington DC, United States.
Shannon R CahalanOncology, Georgetown University, Washington DC, United States.
Xu ShiDepartment of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, United States.
Robert L CopelandDepartment of Pharmacology, College of Medicine, Howard University, Washington, DC, United States.
Bassem R HaddadOncology, Georgetown University, Washington DC, United States.
Mary Beth MartinDepartment of Biochemistry and Molecular and Cellular Biology, Georgetown University, Washington, DC, United States.

Funding

Fatty Liver Disease in African AmericansP20CA242617 · NCI · HOWARD UNIVERSITY · PI TAYLOR, TELETIA RENEE · 2019 to 2022
$1.2M
Fatty Liver Disease in African AmericansP20CA242611 · NCI · GEORGETOWN UNIVERSITY · PI ADAMS-CAMPBELL, LUCILE LAUREN, TAYLOR, TELETIA RENEE · 2019 to 2022
$868k
NCI NIH HHS P20 CA242611NCI NIH HHS P20 CA242617
6 · The paper itself

Abstract

Objective: Estrogen-related receptor γ (ERRγ) is a metabolic regulator with no identified physiological ligands. This study investigates whether calcium is an ERRγ ligand that mediates the effects of glucagon and whether cadmium, which mimics the effects of calcium, disrupts metabolism through ERRγ. Method: HepG2, MCF-7, and HEK293T transfected with ERRγ were treated with glucagon, calcium, cadmium, ERRγ agonist, or ERRγ inhibitor. Cells were then collected for Results: In HepG2 cells, treatment with glucagon, calcium, or cadmium re-localized ERRγ to the cell nucleus, recruited ERRγ to estrogen-related response elements, induced the expression of ERRγ-regulated genes, and increased extracellular glucose that was blocked by an ERRγ antagonist. In MCF-7 cells and HEK293T cells transfected with ERRγ, similar treatments induced the expression of metabolic genes. Mutational analysis identified S303, T429, and E452 in the ligand-binding domain as potential interaction sites. Molecular dynamics simulations showed that calcium induced changes in ERRγ similar to ERRγ agonist. Conclusion: The results suggest that calcium is a potential ligand of ERRγ that mediates the effects of glucagon and cadmium disrupts metabolism through ERRγ.

Indexed as

CadmiumCalciumReceptors, EstrogenGlucagonHEK293 CellsHep G2 CellsHumansMCF-7 CellsMolecular Dynamics SimulationCadmiumCalciumESRRG protein, humanGlucagonReceptors, Estrogencadmiumcalciumestrogen-related receptor γgluconeogenesismetals

Identifiers

PMID39507056
PMCPMC11537906

What OpenQuestion holds

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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.