Evidence map›Paper›PMID 35196069›Full record

ArticleMolecular biology of the cell2022

The methyltransferase enzymes KMT2D, SETD1B, and ASH1L are key mediators of both metabolic and epigenetic changes during cellular senescence.

Timothy Nacarelli, Ashley Azar, Manali Potnis, Gregg Johannes, Joshua Mell, F Brad Johnson, Holly Brown-Borg, Eishi Noguchi, Christian Sell

Open access · greenAbstract read
In one paragraph

Article in Molecular biology of the cell, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

5 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
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

9 authors at 5 institutions in 1 country.

Timothy NacarelliGlaxosmithkline, Oncology Synthetic Lethal Research Unit, Collegeville, PA 19426.
Ashley AzarMerck, West Point, PA 19486.
Manali PotnisDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102.
Gregg JohannesAbsorption Systems LLC, Exton, PA 19341.
Joshua MellDepartment of Microbiology and Immunology, Drexel University College of Medicine, Philadelphia, PA 19129.
F Brad JohnsonDepartment of Pathology, University of Pennsylvania, Philadelphia, PA 19104.
Holly Brown-BorgDepartment of Biomedical Sciences, University of North Dakota School of Medicine and Health Sciences, Grand Forks, ND 58203.
Eishi NoguchiDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102.
Christian SellDepartment of Biochemistry and Molecular Biology, Drexel University College of Medicine, Philadelphia, PA 19102.
Drexel University · USAbsorption Systems (United States) · USUnited States Military Academy · USUniversity of North Dakota · USUniversity of Pennsylvania · US

Funding

IDENTIFICATION AND PRECLINICAL EVALUATION OF NOVEL THERAPEUTIC APPROACHES TO DYSKERATOSIS CONGENITAR01HL148821 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI JOHNSON, F. BRAD, LENGNER, CHRISTOPHER JOACHIM · 2019 to 2022
$2.5M
NHLBI NIH HHS R01 HL148821
6 · The paper itself

Abstract

Cellular senescence is a terminal cell fate characterized by growth arrest and a metabolically active state characterized by high glycolytic activity. Human fibroblasts were placed in a unique metabolic state using a combination of methionine restriction (MetR) and rapamycin (Rapa). This combination induced a metabolic reprogramming that prevented the glycolytic shift associated with senescence. Surprisingly, cells treated in this manner did not undergo senescence but continued to divide at a slow rate even at high passage, in contrast with either Rapa treatment or MetR, both of which extended life span but eventually resulted in growth arrest. Transcriptome-wide analysis revealed a coordinated regulation of metabolic enzymes related to one-carbon metabolism including three methyltransferase enzymes (KMT2D, SETD1B, and ASH1L), key enzymes for both carnitine synthesis and histone modification. These enzymes appear to be involved in both the metabolic phenotype of senescent cells and the chromatin changes required for establishing the senescence arrest. Targeting one of these enzymes, ASH1L, produced both a glycolytic shift and senescence, providing proof of concept. These findings reveal a mechanistic link between a major metabolic hallmark of senescence and nuclear events required for senescence.

Indexed as

Cellular SenescenceEpigenesis, GeneticFibroblastsGlycolysisMethionineSirolimusMethionineSirolimus

Identifiers

PMID35196069
PMCPMC9282020
OpenAlexW4213442803

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.