Evidence map›Paper›PMID 39826697›Full record

ArticleThe Journal of biological chemistry2025

Diet-induced obesity mediated through estrogen-related receptor α is independent of intestinal function.

Kiranmayi Vemuri, Jahangir Iqbal, Sneha Kumar, Alexandra Logerfo, Maria Ibrahim, Eileen White, Michael P Verzi

Abstract read
In one paragraph

Article in The Journal of biological chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Kiranmayi VemuriDepartment of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA.
Jahangir IqbalDepartment of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA.
Sneha KumarDepartment of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA.
Alexandra LogerfoDepartment of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA.
Maria IbrahimRutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA; Ludwig Princeton Branch, Ludwig Institute for Cancer Research, Princeton University, Princeton, New Jersey, USA.
Eileen WhiteRutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA; Ludwig Princeton Branch, Ludwig Institute for Cancer Research, Princeton University, Princeton, New Jersey, USA; Department of Molecular Biology and Biochemistry, Rutgers University, Piscataway, New Jersey, USA.
Michael P VerziDepartment of Genetics, Human Genetics Institute of New Jersey, Rutgers University, Piscataway, New Jersey, USA; Rutgers Cancer Institute of New Jersey, New Brunswick, New Jersey, USA; Rutgers Center for Lipid Research, New Jersey Institute for Food, Nutrition & Health, Rutgers University, New Brunswick, New Jersey, USA; NIEHS Center for Environmental Exposures and Disease (CEED), Rutgers EOHSI Piscataway, New Jersey, USA. Electronic address: verzi@biology.rutgers.edu.

Funding

Rutgers Biotechnology Training ProgramT32GM135141 · NIGMS · RUTGERS, THE STATE UNIV OF N.J. · PI ANN M. STOCK, Martin L Yarmush · 2020 to 2026
$3.5M
Mechanisms Driving Metabolic Shifts in the Intestinal EpitheliumR01DK126446 · NIDDK · RUTGERS, THE STATE UNIV OF N.J. · PI VERZI, MICHAEL P. · 2021 to 2025
$2.1M
Mechanisms of Intestinal Epithelial DifferentiationR01DK121915 · NIDDK · RUTGERS, THE STATE UNIV OF N.J. · PI ELLISON, CHRISTOPHER EUGENE, VERZI, MICHAEL P. · 2020 to 2023
$1.7M
Mechanisms of BMP signaling driving tissue pattern in the intestineF31DK137596 · NIDDK · RUTGERS, THE STATE UNIV OF N.J. · PI LOGERFO, ALEXANDRA · 2024 to 2025
$84k
NIDDK NIH HHS F31 DK137596NIDDK NIH HHS R01 DK121915NIDDK NIH HHS R01 DK126446NIGMS NIH HHS T32 GM135141
6 · The paper itself

Abstract

Obesity has escalated to epidemic proportions, driving significant advances in therapeutic strategies aimed at combating this condition. The estrogen-related receptor α (ESRRA), a transcription factor, plays pivotal roles in energy metabolism across multiple tissues. Research has consistently shown that the absence of Esrra results in notable fat malabsorption and increased resistance to diet-induced obesity. However, existing studies primarily focusing on germline Esrra mutants fail to account for tissue-specific roles of ESRRA in obesity. Notably, Esrra exhibits high expression in the gastrointestinal tract relative to other tissues. Given the gastrointestinal tract's central role in dietary lipid absorption and metabolism, it is critical to investigate how ESRRA specifically affects this tissue. This study aims to fill this gap by employing advanced mouse genetics and genomics techniques to dissect the impact of ESRRA within the intestine. We also aim to elucidate ESRRA's specific contributions to diet-induced obesity and refine our understanding of how this transcription factor influences metabolic outcomes in the context of dietary intake.

Indexed as

Intestinal MucosaIntestinesObesityReceptors, EstrogenAnimalsDiet, High-FatERRalpha Estrogen-Related ReceptorFemaleMaleMiceMice, Inbred C57BLMice, KnockoutERRalpha Estrogen-Related ReceptorReceptors, Estrogenadipose tissuediet-induced obesityepigeneticsestrogen-related receptor αintestinal epitheliumintestinemetabolic diseaseobesityobesity therapeuticstranscription factor

Identifiers

PMID39826697
PMCPMC11849689

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Registered trials

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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.