Evidence map›Paper›PMID 41296708›Full record

ArticlePloS one2025

The histone modification regulator, SIN3, plays a role in the cellular response to changes in glycolytic flux.

Imad Soukar, Anindita Mitra, Linh Vo, Melanie Rofoo, Miriam L Greenberg, Lori A Pile

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Imad SoukarDepartment of Biological Sciences, Wayne State University, Detroit, Michigan, United States of America.
Anindita MitraDepartment of Biological Sciences, Wayne State University, Detroit, Michigan, United States of America.
Linh VoDepartment of Biological Sciences, Wayne State University, Detroit, Michigan, United States of America.ORCID https://orcid.org/0000-0002-0665-0309
Melanie RofooDepartment of Biological Sciences, Wayne State University, Detroit, Michigan, United States of America.
Miriam L GreenbergDepartment of Biological Sciences, Wayne State University, Detroit, Michigan, United States of America.
Lori A PileDepartment of Biological Sciences, Wayne State University, Detroit, Michigan, United States of America.ORCID https://orcid.org/0000-0002-7189-4828

Funding

Tumor Biology and Microenvironment (Program 1)P30CA022453 · NCI · WAYNE STATE UNIVERSITY · PI Julie Lynn Boerner · 1985 to 2026
$68.4M
Translational Research Support CoreP30ES036084 · NIEHS · WAYNE STATE UNIVERSITY · PI Thomas A Kocarek · 2024 to 2026
$5.2M
Regulation of Inositol Biosynthesis and Consequences of Inositol DepletionR35GM149271 · NIGMS · WAYNE STATE UNIVERSITY · PI Miriam L Greenberg · 2023 to 2026
$1.6M
Orbitrap Tribrid Mass Spectrometer for Wayne State ProteomicsS10OD030484 · OD · WAYNE STATE UNIVERSITY · PI STEMMER, PAUL M · 2021 to 2021
$1.3M
NCI NIH HHS P30 CA022453NIEHS NIH HHS P30 ES036084NIGMS NIH HHS R35 GM149271NIH HHS S10 OD030484
6 · The paper itself

Abstract

Epigenetic regulation and metabolism are connected. Epigenetic regulators, like the SIN3 complex, affect the expression of a wide range of genes, including those encoding metabolic enzymes essential for central carbon metabolism. The idea that epigenetic modifiers can sense and respond to metabolic flux by regulating gene expression has long been proposed. In support of this cross-talk, we provide data linking SIN3 regulatory action on a subset of metabolic genes with the cellular response to changes in metabolic flux. Furthermore, we show that loss of SIN3 is linked to decreases in mitochondrial respiration and the cellular response to mitochondrial and glycolytic stress. Data presented here provide evidence that SIN3 is important for the cellular response to metabolic flux change.

Indexed as

GlycolysisSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsEpigenesis, GeneticMitochondriaSin3 Histone Deacetylase and Corepressor ComplexSaccharomyces cerevisiae ProteinsSin3 Histone Deacetylase and Corepressor Complex

Identifiers

PMID41296708
PMCPMC12654916

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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.