Evidence mapPaperPMID 40636718Full record

ArticleFrontiers in aging2025

The lifespan-extending MEK1 inhibitor trametinib promotes regulation of de novo lipogenesis enzymes by chaperone-mediated autophagy.

Jiexian Chen, Joshua Berg, Calvin M Burns, Hanyi Jia, Xinna Li, Richard A Miller, S Joseph Endicott, Gonzalo Garcia

Abstract read
In one paragraph

Article in Frontiers in aging, 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

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

8 authors.

Jiexian ChenDepartment of Chemical Biology, University of Michigan College of Literature, Science, and the Arts, Ann Arbor, MI, United States.
Joshua BergDepartment of Chemical Biology, University of Michigan College of Literature, Science, and the Arts, Ann Arbor, MI, United States.
Calvin M BurnsDepartment of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, United States.
Hanyi JiaDepartment of Molecular, Cell, and Developmental Biology, University of California, Los Angeles, Los Angeles, CA, United States.
Xinna LiDepartment of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, United States.
Richard A MillerDepartment of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, United States.
S Joseph EndicottDepartment of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, United States.
Gonzalo GarciaDepartment of Pathology, University of Michigan School of Medicine, Ann Arbor, MI, United States.

Funding

Research Education CoreP30AG024824 · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 2004 to 2025
$4.4M
Laboratory for Anti-Geric Testing, Evaluation and Resea*U01AG022303 · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 2003 to 2025
$2.7M
Science CoreP20GM121176 · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · 2025 to 2025
$2.2M
NIA NIH HHS P30 AG024824NIA NIH HHS U01 AG022303NIGMS NIH HHS P20 GM121176
6 · The paper itself

Abstract

The availability of multiple slow-aging mice allows a search for possible shared mechanisms that affect the rate of aging. Previous work has shown downregulation of the MEK1-ERK-MNK kinase cascade, which regulates protein translation through eIF4E, in response to four anti-aging drugs. Here we show that decreased protein abundance of enzymes involved in hepatic

Indexed as

agingchaperone-mediated autophagy (CMA)extracellular signal-regulated kinase (ERK)lifespanlongevitysignal transductiontranscriptional response

Identifiers

PMID40636718
PMCPMC12237883

What Socratic holds

Textmetadata
LicenceCC BY
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.