Evidence map›Paper›PMID 37055547›Full record

ReviewNature reviews. Endocrinology2023

The role of ChREBP in carbohydrate sensing and NAFLD development.

Marion Régnier, Thaïs Carbinatti, Lucia Parlati, Fadila Benhamed, Catherine Postic

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 57 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
57citing papers in PubMed, 2 pooled it
27.3field-weighted citation impact, top 1% 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

57 citing papers in PubMed, 2 syntheses or guidelines pooled it, 86 citations in OpenAlex.

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  20. Role of ChREBP-PPARα-FGF21 Axis in Metabolic Dysfunction of MASLD.International journal of molecular sciences · 2025
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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

5 authors at 3 institutions in 1 country.

Marion RégnierUniversité Paris Cité, Institut Cochin, CNRS, INSERM, Paris, France. marion.regnier@inserm.fr.
Thaïs CarbinattiUniversité Paris Cité, Institut Cochin, CNRS, INSERM, Paris, France.
Lucia ParlatiUniversité Paris Cité, Institut Cochin, CNRS, INSERM, Paris, France.
Fadila BenhamedUniversité Paris Cité, Institut Cochin, CNRS, INSERM, Paris, France.
Catherine PosticUniversité Paris Cité, Institut Cochin, CNRS, INSERM, Paris, France. catherine.postic@inserm.fr.
Institut Cochin · FRUniversité Paris Cité · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Excessive sugar consumption and defective glucose sensing by hepatocytes contribute to the development of metabolic diseases including type 2 diabetes mellitus (T2DM) and nonalcoholic fatty liver disease (NAFLD). Hepatic metabolism of carbohydrates into lipids is largely dependent on the carbohydrate-responsive element binding protein (ChREBP), a transcription factor that senses intracellular carbohydrates and activates many different target genes, through the activation of de novo lipogenesis (DNL). This process is crucial for the storage of energy as triglycerides in hepatocytes. Furthermore, ChREBP and its downstream targets represent promising targets for the development of therapies for the treatment of NAFLD and T2DM. Although lipogenic inhibitors (for example, inhibitors of fatty acid synthase, acetyl-CoA carboxylase or ATP citrate lyase) are currently under investigation, targeting lipogenesis remains a topic of discussion for NAFLD treatment. In this Review, we discuss mechanisms that regulate ChREBP activity in a tissue-specific manner and their respective roles in controlling DNL and beyond. We also provide in-depth discussion of the roles of ChREBP in the onset and progression of NAFLD and consider emerging targets for NAFLD therapeutics.

Indexed as

Diabetes Mellitus, Type 2Non-alcoholic Fatty Liver DiseaseBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarbohydratesHumansLiverTranscription FactorsBasic Helix-Loop-Helix Leucine Zipper Transcription FactorsCarbohydratesMLXIPL protein, humanTranscription Factors

Identifiers

PMID37055547
OpenAlexW4365479160

What Socratic 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 Socratic graph.