Evidence map›Paper›PMID 30044176›Full record

ArticleStem cells and development2018

p53 Is Active in Human Amniotic Fluid Stem Cells.

Melissa Rodrigues, Ivana Antonucci, Seham Elabd, Shilpa Kancherla, Marco Marchisio, Christine Blattner, Liborio Stuppia

Open access · hybridAbstract read
In one paragraph

Article in Stem cells and development, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.8field-weighted citation impact, top 13% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Amniotic Fluid Cells, Stem Cells, and p53: Can We Stereotype p53 Functions?International journal of molecular sciences · 2019
    Review
  7. Article
  8. 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

7 authors at 2 institutions in 3 countries.

Melissa Rodrigues1 Laboratory of Molecular Genetics, Department of Psychological, Health and Territorial Sciences, School of Medicine and Health Sciences, G. d' Annunzio University , Chieti-Pescara, Italy .
Ivana Antonucci1 Laboratory of Molecular Genetics, Department of Psychological, Health and Territorial Sciences, School of Medicine and Health Sciences, G. d' Annunzio University , Chieti-Pescara, Italy .
Seham Elabd2 Institute of Toxicology and Genetics, Karlsruhe Institute of Technology , Karlsruhe, Germany .
Shilpa Kancherla2 Institute of Toxicology and Genetics, Karlsruhe Institute of Technology , Karlsruhe, Germany .
Marco Marchisio3 Centre of Aging Science and Translational Medicine (Ce.S.I.-Me.T.), G. d'Annunzio University , Chieti-Pescara, Italy .
Christine Blattner2 Institute of Toxicology and Genetics, Karlsruhe Institute of Technology , Karlsruhe, Germany .
Liborio Stuppia1 Laboratory of Molecular Genetics, Department of Psychological, Health and Territorial Sciences, School of Medicine and Health Sciences, G. d' Annunzio University , Chieti-Pescara, Italy .
Karlsruhe Institute of Technology · DEUniversity of Chieti-Pescara · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite increasing interest in human amniotic fluid cells, very little is known about the regulation and function of p53 in this cell type. In this study, we show that undifferentiated human amniotic fluid cells express p53, yet at lower levels than in cancer cells. The p53 protein in amniotic fluid cells is mainly localized in the nuclei, however, its antiproliferative activity is compromised in these cells. Igf2, a maternal imprinted gene, and c-jun, a proto-oncogene, are regulated by p53 in these cells. DNA damage leads to an increase in p53 abundance in human amniotic fluid cells and to transcriptional activation of its target genes. Interestingly, cell differentiation toward the neural lineage leads to p53 induction as differentiation progresses.

Indexed as

Amniotic FluidCell DifferentiationCell LineCell NucleusCell ProliferationDNA DamageGene Expression Regulation, DevelopmentalGenomic ImprintingHumansInsulin-Like Growth Factor IIJNK Mitogen-Activated Protein KinasesNeuronsProto-Oncogene MasStem CellsTumor Suppressor Protein p53IGF2 protein, humanInsulin-Like Growth Factor IIJNK Mitogen-Activated Protein KinasesMAS1 protein, humanProto-Oncogene MasTP53 protein, humanTumor Suppressor Protein p53amniotic fluid cellsapoptosisdifferentiationDNA damage responsep53proliferation

Identifiers

PMID30044176
PMCPMC6209428
OpenAlexW2884282655

What OpenQuestion 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 OpenQuestion graph.