Evidence map›Paper›PMID 31531979›Full record

ReviewFEBS letters2019

The paradox of metabolism in quiescent stem cells.

Hilary A Coller

Abstract readReview
In one paragraph

Review in FEBS letters, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed, 1 pooled it
–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

51 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. The dynamics of centromere assembly and disassembly during quiescence.bioRxiv : the preprint server for biology · 2025
    Article
  11. Quiescence Multiverse.Biomolecules · 2025
    Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Redox regulation of meristem quiescence: outside/in.Journal of experimental botany · 2024
    Review
  17. Article
  18. Article
  19. Review
  20. Article
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

1 author.

Hilary A CollerDepartment of Molecular, Cell and Developmental Biology, University of California, Los Angeles, CA, USA.ORCID 0000-0003-0992-6494

Funding

Metabolic Control of Hair Follicle Stem Cell Homeostasis and TumorigenesisR01AR070245 · NIAMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI CHRISTOFK, HEATHER, LOWRY, WILLIAM E · 2018 to 2022
$2.1M
The Role of Stromal Autophagy in Cutaneous MelanomaR01CA221296 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COLLER, HILARY A · 2018 to 2022
$1.8M
The Role of MicroRNAs in Cellular QuiescenceR01GM081686 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COLLER, HILARY A · 2008 to 2012
$1.4M
A Combined Computational and Experimental Approach to Defining Mechanisms of micrR01GM086465 · NIGMS · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI COLLER, HILARY A · 2009 to 2012
$1.1M
Role of Tumor and Stromal Cell Metabolism in Stress Adaptation and ProgressionRC1CA147961 · NCI · RUTGERS, THE STATE UNIV OF N.J. · PI COLLER, HILARY A, RABINOWITZ, JOSHUA D · 2009 to 2010
$1.0M
Broad Stem Cell CenterCancer Research InstituteClinical Translational Science InstituteDavid Geffen School of Medicine Metabolism Theme AwardJonsson Comprehensive Cancer CenterMelanoma Research AllianceNCI NIH HHS R01 CA221296NCI NIH HHS RC1 CA147961NIAMS NIH HHS R01 AR070245NIGMS NIH HHS R01 GM081686NIGMS NIH HHS R01 GM086465NIH HHS 1 R01 AR070245-01A1Prostate Cancer Spore at UCLAUniversity of California Cancer Research Coordinating Committee
6 · The paper itself

Abstract

The shift between a proliferating and a nonproliferating state is associated with significant changes in metabolic needs. Proliferating cells tend to have higher metabolic rates, and their metabolic profiles facilitate biosynthesis, as compared to those of nondividing cells of the same sort. Recent studies have elucidated specific molecules that control metabolic changes while cells shift between proliferation and quiescence. Embryonic stem cells, which are rapidly proliferating, tend to have metabolic patterns that are similar to those of nonstem cells in a proliferative state. Moreover, although adult stem cells tend to be quiescent, their metabolic profiles have been reported in multiple organs to more closely resemble those of proliferating than those of nondividing cells in some respects. The findings raise questions about whether there are metabolic profiles that are required for stemness, and whether these profiles relate to the metabolic properties that may be required for quiescence. Here, we review the literature on how metabolism changes upon commitment to proliferation and compare the proliferating and nonproliferating metabolic states of differentiated cells and embryonic and adult stem cells.

Indexed as

Cell DivisionOxidative PhosphorylationAdult Stem CellsAmino AcidsAnimalsCell DifferentiationCell LineageCell ProliferationEmbryonic Stem CellsFatty AcidsFibroblastsGlycolysisHumansNeuronsNucleotidesAmino AcidsFatty AcidsNucleotidescell cycleepigeneticsfatty acid metabolismglutamine metabolismglycolysismetabolismnucleotide metabolismoxidative phosphorylationquiescencestem cells

Identifiers

PMID31531979
PMCPMC7034665

What OpenQuestion holds

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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.