Evidence map›Paper›PMID 34968225›Full record

ReviewEpigenomes2019

Metabolic-Epigenetic Axis in Pluripotent State Transitions.

Cristina D'Aniello, Federica Cermola, Eduardo J Patriarca, Gabriella Minchiotti

Abstract readReview
In one paragraph

Review in Epigenomes, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

  1. Review
  2. Article
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  5. Article
  6. Article
  7. Review
  8. Epigenetic and Metabolic Regulation of Macrophages during Gout.Gout, urate, and crystal deposition disease · 2023
    Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. The Multifaceted Roles of Proline in Cell Behavior.Frontiers in cell and developmental biology · 2021
    Review
  15. Article
  16. 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

4 authors.

Cristina D'AnielloStem Cell Fate Laboratory, Institute of Genetics and Biophysics "Adriano Buzzati-Traverso", CNR, 80131 Naples, Italy.
Federica CermolaStem Cell Fate Laboratory, Institute of Genetics and Biophysics "Adriano Buzzati-Traverso", CNR, 80131 Naples, Italy.ORCID 0000-0002-5391-5293
Eduardo J PatriarcaStem Cell Fate Laboratory, Institute of Genetics and Biophysics "Adriano Buzzati-Traverso", CNR, 80131 Naples, Italy.
Gabriella MinchiottiStem Cell Fate Laboratory, Institute of Genetics and Biophysics "Adriano Buzzati-Traverso", CNR, 80131 Naples, Italy.ORCID 0000-0003-0225-9043

Funding

Associazione Italiana per la Ricerca sul Cancro IG 20736Ministero dell'Istruzione, dell'Università e della Ricerca CTN01_00177POR Campania FESR 2014/2020 SATIN
6 · The paper itself

Abstract

Cell state transition (CST) occurs during embryo development and in adult life in response to different stimuli and is associated with extensive epigenetic remodeling. Beyond growth factors and signaling pathways, increasing evidence point to a crucial role of metabolic signals in this process. Indeed, since several epigenetic enzymes are sensitive to availability of specific metabolites, fluctuations in their levels may induce the epigenetic changes associated with CST. Here we analyze how fluctuations in metabolites availability influence DNA/chromatin modifications associated with pluripotent stem cell (PSC) transitions. We discuss current studies and focus on the effects of metabolites in the context of naïve to primed transition, PSC differentiation and reprogramming of somatic cells to induced pluripotent stem cells (iPSCs), analyzing their mechanism of action and the causal correlation between metabolites availability and epigenetic alteration.

Indexed as

DNA and histone methylationhistone acetylationmetabolites availabilitypluripotent stem cell transitions

Identifiers

PMID34968225
PMCPMC8594706

What OpenQuestion holds

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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.