Evidence map›Paper›PMID 36787804›Full record

ArticleInternational journal of sports medicine2023

Estrogen-related Receptor Signaling in Skeletal Muscle Fitness.

Danesh Sopariwala, Hao Nguyen, Vihang Narkar

Open access · greenAbstract read
In one paragraph

Article in International journal of sports medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

6 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Estrogen-Related Receptor Alpha Promotes Skeletal Muscle Regeneration and Mitigates Muscular Dystrophy.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2025
    Article
  4. Article
  5. Review
  6. Review
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

3 authors at 1 institution in 1 country.

Danesh SopariwalaInstitute of Molecular Medicine, University of Texas John P and Katherine G McGovern Medical School, Houston, United States.
Hao NguyenInstitute of Molecular Medicine, University of Texas John P and Katherine G McGovern Medical School, Houston, United States.
Vihang NarkarInstitute of Molecular Medicine, University of Texas John P and Katherine G McGovern Medical School, Houston, United States.
The University of Texas Health Science Center · US

Funding

New therapeutic strategies for Peripheral Arterial DiseaseR01HL152108 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI NARKAR, VIHANG A · 2021 to 2024
$1.8M
Regulation of angiogenesis by nuclear receptors and cofactorsR01HL129191 · NHLBI · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI NARKAR, VIHANG A · 2015 to 2018
$1.7M
NHLBI NIH HHS R01 HL129191NHLBI NIH HHS R01 HL152108
6 · The paper itself

Abstract

Skeletal muscle is a highly plastic tissue that can alter its metabolic and contractile features, as well as regenerative potential in response to exercise and other conditions. Multiple signaling factors including metabolites, kinases, receptors, and transcriptional factors have been studied in the regulation of skeletal muscle plasticity. Recently, estrogen-related receptors (ERRs) have emerged as a critical transcriptional hub in control of skeletal muscle homeostasis. ERRα and ERRγ - the two highly expressed ERR sub-types in the muscle respond to various extracellular cues such as exercise, hypoxia, fasting and dietary factors, in turn regulating gene expression in the skeletal muscle. On the other hand, conditions such as diabetes and muscular dystrophy suppress expression of ERRs in the skeletal muscle, likely contributing to disease progression. We highlight key functions of ERRs in the skeletal muscle including the regulation of fiber type, mitochondrial metabolism, vascularization, and regeneration. We also describe how ERRs are regulated in the skeletal muscle, and their interaction with important muscle regulators (e. g. AMPK and PGCs). Finally, we identify critical gaps in our understanding of ERR signaling in the skeletal muscle, and suggest future areas of investigation to advance ERRs as potential targets for function promoting therapeutics in muscle diseases.

Indexed as

Muscle, SkeletalTranscription FactorsEstrogensHomeostasisHumansSignal TransductionEstrogensTranscription Factors

Identifiers

PMID36787804
PMCPMC11168301
OpenAlexW4320712221

What Socratic 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 Socratic graph.