Evidence map›Paper›PMID 42645229›Full record

ReviewCells2026

AMPK Therapy-A Little Goes A Long Way.

Hannah Ceballos, Eryun Zhang, Wendong Huang

Abstract readReview
In one paragraph

Review in Cells, 2026. 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

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.

Hannah CeballosDepartment of Diabetes Complications, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA.ORCID 0009-0002-5229-4904
Eryun ZhangDepartment of Diabetes Complications, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA.
Wendong HuangDepartment of Diabetes Complications, Beckman Research Institute of City of Hope, Duarte, CA 91010, USA.ORCID 0000-0003-3735-9466

Funding

Bile acids and metabolic surgeryR01DK124627 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI HUANG, WENDONG · 2020 to 2024
$2.0M
Targeting bile acid composition to treat metabolic diseasesR01DK138665 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI WENDONG HUANG, John Jefferson Perry · 2024 to 2026
$1.9M
DIABETES PREVENTION / RISK / OMICS / METABOLISM / THERAPY (PROMT) INTERDISCIPLINARY TRAININGT32DK131943 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI RAMA NATARAJAN, Debbie C Thurmond · 2023 to 2026
$478k
The gut-fat crosstalk in metabolic regulationK01DK142039 · NIDDK · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI ERYUN ZHANG · 2025 to 2026
$280k
NIDDK NIH HHS K01 DK142039NIDDK NIH HHS R01 DK124627NIDDK NIH HHS R01 DK138665NIDDK NIH HHS T32 DK131943
6 · The paper itself

Abstract

AMP-activated protein kinase (AMPK) is a highly conserved serine/threonine kinase that integrates energetic, nutrient, hormonal, redox, and stress signals to coordinate cellular and whole-body energy homeostasis. Although AMPK was initially characterized primarily as a sensor of changes in cellular AMP/ATP ratios, recent studies have revealed additional layers of regulation involving upstream kinases, post-translational modifications, heterotrimeric isoform composition, subcellular compartmentalization, and tissue-specific signaling. In this review, we provide an updated overview of the molecular mechanisms regulating AMPK activity, its major downstream metabolic and homeostatic pathways, its roles in metabolic, cardiovascular, neurodegenerative, muscular, malignant, and age-associated diseases, and current strategies for pharmacological AMPK modulation. We compare indirect activators, including metformin and naturally derived compounds, with direct small-molecule agonists targeting the allosteric drug and metabolite (ADaM) site, and emerging activators that selectively engage specific AMPK isoforms, tissues, or subcellular pools. We also discuss endogenous AMPK regulators, including microbiota-derived metabolites, and critically evaluate the potential adverse consequences of sustained or systemic AMPK activation. Collectively, current evidence indicates that the therapeutic effects of AMPK activation are highly dependent on tissue, heterotrimer composition, subcellular localization, disease stage, and the magnitude and duration of activation. Rather than indiscriminate systemic activation, future AMPK-directed therapies are therefore likely to benefit from isoform-, tissue-, and compartment-selective approaches that preferentially engage disease-relevant AMPK signaling while minimizing off-target effects. Continued characterization of AMPK signaling specificity and the development of selective pharmacological modulators should facilitate the translation of AMPK biology into more precise therapies for metabolic and other chronic diseases.

Indexed as

AMP-Activated Protein KinasesAnimalsEnergy MetabolismEnzyme ActivationHumansMetforminSignal TransductionAMP-Activated Protein KinasesMetforminAMP-activated protein kinaseAMPKdirect AMPK activatorsenergy metabolismmetabolic diseasesmetformintissue-specific signaling

Identifiers

PMID42645229
PMCPMC13511590

What OpenQuestion 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 OpenQuestion graph.