Evidence map›Paper›PMID 19823043›Full record

ArticleCell cycle (Georgetown, Tex.)2009

microRNAs regulate human embryonic stem cell division.

Junlin Qi, Jenn-Yah Yu, Halyna R Shcherbata, Julie Mathieu, Amy Jia Wang, Sudeshna Seal, Wenyu Zhou, Bradford M Stadler, David Bourgin, Linlin Wang and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell cycle (Georgetown, Tex.), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed
7.3field-weighted citation impact, top 2% 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

86 citing papers in PubMed, 160 citations in OpenAlex.

  1. Article
  2. Posttranscriptional Regulation of Intestinal Mucosal Growth and Adaptation by Noncoding RNAs in Critical Surgical Disorders.Journal of investigative surgery : the official journal of the Academy of Surgical Research · 2024
    Review
  3. Review
  4. Review
  5. Review
  6. Downregulation ofInternational journal of molecular sciences · 2023
    Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Review
  12. Review
  13. microRNAs Regulating Human and Mouse Naïve Pluripotency.International journal of molecular sciences · 2019
    Article
  14. Roles of MicroRNAs in Establishing and Modulating Stem Cell Potential.International journal of molecular sciences · 2019
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. MicroRNAs - novel biomarkers for malignant pleural effusions.Contemporary oncology (Poznan, Poland) · 2019
    Review
  20. Article

26 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

20 authors at 5 institutions in 5 countries.

Junlin QiDepartment of Biochemistry and Institute for Stem Cell and Regenerative Medicine, University of Washington, Seattle, WA, USA.
Jenn-Yah Yu
Halyna R Shcherbata
Julie Mathieu
Amy Jia Wang
Sudeshna Seal
Wenyu Zhou
Bradford M Stadler
David Bourgin
Linlin Wang
Angel Nelson
Carol Ware
Christopher Raymond
Lee P Lim
Jill Magnus
Irena Ivanovska
Robert Diaz
Alexey Ball
Michele A Cleary
Hannele Ruohola-Baker
University of Washington · USMerck (Japan) · JPMax Planck Institute for Biophysical Chemistry · DEMercy University Hospital · IENational Yang Ming Chiao Tung University · TW

Funding

MicroRNA Function in Human Embryonic Stem CellsR01GM083867 · NIGMS · UNIVERSITY OF WASHINGTON · PI RUOHOLA-BAKER, HANNELE · 2008 to 2011
$1.5M
NIGMS NIH HHS R01 GM083867
6 · The paper itself

Abstract

microRNAs (miRNAs) regulate numerous physiological processes such as cell division and differentiation in many tissue types including stem cells. To probe the role that miRNAs play in regulating processes relevant to embryonic stem cell biology, we used RNA interference to silence DICER and DROSHA, the two main miRNA processing enzymes. Consistent with a role for miRNAs in maintaining normal stem cell division and renewal, we found that perturbation of miRNA pathway function in human embryonic stem cells (hESCs) attenuates cell proliferation. Normal cell growth can be partially restored by introduction of the mature miRNAs miR-195 and miR-372. These miRNAs regulate two tumor suppressor genes, respectively: WEE1, which encodes a negative G2/M kinase modulator of the CycB/CDK complex and CDKN1A, which encodes p21, a CycE/CDK cyclin dependent kinase inhibitor that regulates the G1/S transition. We show that in wild-type hESCs, WEE 1 levels control the rate of hESC division, whereas p21 levels must be maintained at a low level for hESC division to proceed. These data support a model for hESC cell cycle control in which miRNAs regulate negative cell cycle modulators at two phases of the cell cycle to ensure proper replenishment of the stem cell population.

Indexed as

Models, BiologicalBase SequenceBlotting, WesternCell Cycle ProteinsCell DivisionCyclin-Dependent Kinase Inhibitor p21Embryonic Stem CellsHumansMicroarray AnalysisMicroRNAsMolecular Sequence DataNuclear ProteinsOligonucleotidesProtein-Tyrosine KinasesRibonuclease IIIRNA InterferenceCDKN1A protein, humanCell Cycle ProteinsCyclin-Dependent Kinase Inhibitor p21DROSHA protein, humanMicroRNAsNuclear ProteinsOligonucleotidesProtein-Tyrosine KinasesRibonuclease IIIWEE1 protein, human

Identifiers

PMID19823043
PMCPMC2925126
OpenAlexW1979364059

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.