Evidence map›Paper›PMID 22862944›Full record

ArticleCell stem cell2012

Regulation of embryonic and induced pluripotency by aurora kinase-p53 signaling.

Dung-Fang Lee, Jie Su, Yen-Sin Ang, Xonia Carvajal-Vergara, Sonia Mulero-Navarro, Carlos F Pereira, Julian Gingold, Hung-Liang Wang, Ruiying Zhao, Ana Sevilla and 15 more

Abstract read
In one paragraph

Article in Cell stem cell, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 96 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
96citing papers in PubMed, 2 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

96 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
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  5. Review
  6. Article
  7. Article
  8. Rewired mNature communications · 2023
    Article
  9. International journal of biological sciences · 2023
    Article
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  12. Review
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  15. Review
  16. Article
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  18. Observational
  19. Article
  20. The Basally Expressed p53-Mediated Homeostatic Function.Frontiers in cell and developmental biology · 2021
    Review

36 more citing papers are in PubMed but not listed here.

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

25 authors.

Dung-Fang LeeDepartment of Developmental and Regenerative Biology and The Black Family Stem Cell Institute, Mount Sinai School of Medicine, New York, NY 10029, USA.
Jie Su
Yen-Sin Ang
Xonia Carvajal-Vergara
Sonia Mulero-Navarro
Carlos F Pereira
Julian Gingold
Hung-Liang Wang
Ruiying Zhao
Ana Sevilla
Henia Darr
Andrew J K Williamson
Betty Chang
Xiaohong Niu
Francesca Aguilo
Elsa R Flores
Yuh-Pyng Sher
Mien-Chie Hung
Anthony D Whetton
Bruce D Gelb
Kateri A Moore
Hans-Willem Snoeck
Avi Ma'ayan
Christoph Schaniel
Ihor R Lemischka

Funding

System Biology Center in New YorkP50GM071558 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ZAPH, SUSANA NEVES · 2007 to 2017
$22.8M
Global & Systems Level Analyses of Cell Fate RegulationR01GM078465 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LEMISCHKA, IHOR R · 2007 to 2015
$3.7M
Interdisciplinary Training in Systems and Developmental Biology and Birth DefectsT32HD075735 · NICHD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI JABS, ETHYLIN WANG · 2013 to 2022
$1.8M
Expression2Kinases: mRNA Profiling Linked to Multiple Upstream Regulatory LayersR01GM098316 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MA'AYAN, AVI · 2012 to 2015
$1.3M
NICHD NIH HHS T32 HD075735NIGMS NIH HHS 5R01GM078465NIGMS NIH HHS P50 GM071558NIGMS NIH HHS R01 GM078465NIGMS NIH HHS R01 GM098316
6 · The paper itself

Abstract

Many signals must be integrated to maintain self-renewal and pluripotency in embryonic stem cells (ESCs) and to enable induced pluripotent stem cell (iPSC) reprogramming. However, the exact molecular regulatory mechanisms remain elusive. To unravel the essential internal and external signals required for sustaining the ESC state, we conducted a short hairpin (sh) RNA screen of 104 ESC-associated phosphoregulators. Depletion of one such molecule, aurora kinase A (Aurka), resulted in compromised self-renewal and consequent differentiation. By integrating global gene expression and computational analyses, we discovered that loss of Aurka leads to upregulated p53 activity that triggers ESC differentiation. Specifically, Aurka regulates pluripotency through phosphorylation-mediated inhibition of p53-directed ectodermal and mesodermal gene expression. Phosphorylation of p53 not only impairs p53-induced ESC differentiation but also p53-mediated suppression of iPSC reprogramming. Our studies demonstrate an essential role for Aurka-p53 signaling in the regulation of self-renewal, differentiation, and somatic cell reprogramming.

Indexed as

Signal TransductionAnimalsAurora Kinase AAurora KinasesCell DifferentiationCell LineCell ProliferationEmbryonic Stem CellsHEK293 CellsHumansMiceMice, KnockoutPhosphorylationPluripotent Stem CellsProtein Serine-Threonine KinasesTumor Suppressor Protein p53AURKA protein, humanAurka protein, mouseAurora Kinase AAurora KinasesProtein Serine-Threonine KinasesTumor Suppressor Protein p53

Identifiers

PMID22862944
PMCPMC3413175

What OpenQuestion holds

Textmetadata
LicenceTDM
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.