Evidence map›Paper›PMID 25501598›Full record

ArticleCell death and differentiation2015

Suppression of epithelial-mesenchymal transition and apoptotic pathways by miR-294/302 family synergistically blocks let-7-induced silencing of self-renewal in embryonic stem cells.

W-T Guo, X-W Wang, Y-L Yan, Y-P Li, X Yin, Q Zhang, C Melton, A Shenoy, N A Reyes, S A Oakes and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

27 citing papers in PubMed, 38 citations in OpenAlex.

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  8. miRNAs as Biomarkers in Diabetes: Moving towards Precision Medicine.International journal of molecular sciences · 2022
    Review
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  14. Review
  15. Article
  16. Roles of MicroRNAs in Establishing and Modulating Stem Cell Potential.International journal of molecular sciences · 2019
    Review
  17. Article
  18. Review
  19. Article
  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

12 authors at 5 institutions in 2 countries.

W-T GuoPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
X-W WangPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
Y-L YanPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
Y-P LiPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
X YinPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
Q ZhangPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
C MeltonDepartment of Urology, Center of Reproductive Sciences, and the Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
A ShenoyDepartment of Urology, Center of Reproductive Sciences, and the Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
N A ReyesDepartment of Pathology and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
S A OakesDepartment of Pathology and Helen Diller Family Comprehensive Cancer Center, University of California, San Francisco, CA, USA.
R BlellochDepartment of Urology, Center of Reproductive Sciences, and the Eli and Edythe Broad Center for Regeneration Medicine and Stem Cell Research, University of California, San Francisco, CA, USA.
Y WangPeking-Tsinghua Center for Life Sciences, Institute of Molecular Medicine, Peking University, Beijing, China.
Center for Life Sciences · CNPeking University · CNUniversity of California, San Francisco · USBroad Center · USUCSF Helen Diller Family Comprehensive Cancer Center · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI KRUMMEL, MATTHEW F · 2003 to 2019
$21.8M
Signaling Cell Death from the Endoplasmic ReticulumR01CA136577 · NCI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI OAKES, SCOTT A. · 2009 to 2013
$1.6M
Attenuating ER and oxidative stress signaling to reduce cell degeneration in vivoR01DK095306 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI OAKES, SCOTT A., PAPA, FEROZ R · 2013 to 2016
$1.5M
Small RNAs in Stem Cell Differentiation and Neural DevelopmentR01NS057221 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLELLOCH, ROBERT · 2007 to 2010
$1.4M
MicroRNA Based Pathway Discovery in Cellular ReprogrammingR01GM101180 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BLELLOCH, ROBERT · 2012 to 2015
$1.4M
NCI NIH HHS R01 CA136577NCI NIH HHS R01CA136577NIDDK NIH HHS P30 DK063720NIDDK NIH HHS R01 DK095306NIDDK NIH HHS R01DK095306NIGMS NIH HHS GM101180NIGMS NIH HHS R01 GM101180NINDS NIH HHS R01 NS057221
6 · The paper itself

Abstract

The embryonic stem cell (ESC)-enriched miR-294/302 family and the somatic cell-enriched let-7 family stabilizes the self-renewing and differentiated cell fates, respectively. The mechanisms underlying these processes remain unknown. Here we show that among many pathways regulated by miR-294/302, the combinatorial suppression of epithelial-mesenchymal transition (EMT) and apoptotic pathways is sufficient in maintaining the self-renewal of ESCs. The silencing of ESC self-renewal by let-7 was accompanied by the upregulation of several EMT regulators and the induction of apoptosis. The ectopic activation of either EMT or apoptotic program is sufficient in silencing ESC self-renewal. However, only combined but not separate suppression of the two programs inhibited the silencing of ESC self-renewal by let-7 and several other differentiation-inducing miRNAs. These findings demonstrate that combined repression of the EMT and apoptotic pathways by miR-294/302 imposes a synergistic barrier to the silencing of ESC self-renewal, supporting a model whereby miRNAs regulate complicated cellular processes through synergistic repression of multiple targets or pathways.

Indexed as

AnimalsApoptosisCell Self RenewalEmbryonic Stem CellsEpithelial-Mesenchymal TransitionMiceMicroRNAsSignal TransductionMicroRNAsMIRN294 microRNA, mouseMIRN302 microRNA, mousemirnlet7 microRNA, mouse

Identifiers

PMID25501598
PMCPMC4572863
OpenAlexW1995772731

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.