Evidence map›Paper›PMID 36429035›Full record

ReviewCells2022

Stemness of Normal and Cancer Cells: The Influence of Methionine Needs and SIRT1/PGC-1α/PPAR-α Players.

Youssef Siblini, Farès Namour, Abderrahim Oussalah, Jean-Louis Guéant, Céline Chéry

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

11 citing papers in PubMed, 14 citations in OpenAlex.

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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 1 institution in 1 country.

Youssef SibliniINSERM, UMR_S1256, NGERE-Nutrition, Genetics, Environmental Risk Exposure, University of Lorraine, 54500 Vandoeuvre-lès-Nancy, France.
Farès NamourINSERM, UMR_S1256, NGERE-Nutrition, Genetics, Environmental Risk Exposure, University of Lorraine, 54500 Vandoeuvre-lès-Nancy, France.
Abderrahim OussalahINSERM, UMR_S1256, NGERE-Nutrition, Genetics, Environmental Risk Exposure, University of Lorraine, 54500 Vandoeuvre-lès-Nancy, France.ORCID 0000-0002-9731-4529
Jean-Louis GuéantINSERM, UMR_S1256, NGERE-Nutrition, Genetics, Environmental Risk Exposure, University of Lorraine, 54500 Vandoeuvre-lès-Nancy, France.ORCID 0000-0002-5067-042X
Céline ChéryINSERM, UMR_S1256, NGERE-Nutrition, Genetics, Environmental Risk Exposure, University of Lorraine, 54500 Vandoeuvre-lès-Nancy, France.
Nutrition-Génétique et Exposition aux Risques Environnementaux

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Stem cells are a population of undifferentiated cells with self-renewal and differentiation capacities. Normal and cancer stem cells share similar characteristics in relation to their stemness properties. One-carbon metabolism (OCM), a network of interconnected reactions, plays an important role in this dependence through its role in the endogenous synthesis of methionine and S-adenosylmethionine (SAM), the universal donor of methyl groups in eukaryotic cells. OCM genes are differentially expressed in stem cells, compared to their differentiated counterparts. Furthermore, cultivating stem cells in methionine-restricted conditions hinders their stemness capacities through decreased SAM levels with a subsequent decrease in histone methylation, notably H3K4me3, with a decrease in stem cell markers. Stem cells' reliance on methionine is linked to several mechanisms, including high methionine flux or low endogenous methionine biosynthesis. In this review, we provide an overview of the recent discoveries concerning this metabolic dependence and we discuss the mechanisms behind them. We highlight the influence of SIRT1 on SAM synthesis and suggest a role of PGC-1α/PPAR-α in impaired stemness produced by methionine deprivation. In addition, we discuss the potential interest of methionine restriction in regenerative medicine and cancer treatment.

Indexed as

MethionineNeoplasmsNeoplastic Stem CellsPPAR alphaRacemethionineS-AdenosylmethionineSirtuin 1MethioninePPAR alphaRacemethionineS-AdenosylmethionineSirtuin 1cancer stem cellsmethioninemethionine dependencenormal stem cellsperoxisome proliferator-activated receptor alphaperoxisome proliferator-activated receptor gamma coactivator 1-alphaS-adenosylmethioninesirtuin 1stemness

Identifiers

PMID36429035
PMCPMC9688847
OpenAlexW4309214340

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.