Evidence map›Paper›PMID 25406066›Full record

ArticleeLife2014

miR-142 regulates the tumorigenicity of human breast cancer stem cells through the canonical WNT signaling pathway.

Taichi Isobe, Shigeo Hisamori, Daniel J Hogan, Maider Zabala, David G Hendrickson, Piero Dalerba, Shang Cai, Ferenc Scheeren, Angera H Kuo, Shaheen S Sikandar and 8 more

Abstract read
In one paragraph

Article in eLife, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 107 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
107citing papers in PubMed, 1 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

107 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
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  5. Review
  6. Review
  7. Organoids in breast cancer translational research: intersection of technologies.Translational breast cancer research : a journal focusing on translational research in breast cancer · 2025
    Review
  8. Non-Coding RNAs in Breast Cancer: Diagnostic and Therapeutic Implications.International journal of molecular sciences · 2024
    Review
  9. Article
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  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
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  18. Article
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47 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

18 authors.

Taichi IsobeInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Shigeo HisamoriInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Daniel J HoganDepartment of Biochemistry, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, United States.
Maider ZabalaInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
David G HendricksonDepartment of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, United States.
Piero DalerbaInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Shang CaiInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Ferenc ScheerenInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Angera H KuoInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Shaheen S SikandarInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Jessica S LamInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Dalong QianInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Frederick M DirbasDepartment of Surgery, Stanford University School of Medicine, Stanford, United States.
George SomloCity of Hope Cancer Center, Duarte, United States.
Kaiqin LaoApplied Biosystems, Foster City, United States.
Patrick O BrownDepartment of Biochemistry, Howard Hughes Medical Institute, Stanford University School of Medicine, Stanford, United States.
Michael F ClarkeInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.
Yohei ShimonoInstitute for Stem Cell Biology and Regenerative Medicine, Stanford University, Stanford, United States.

Funding

therapeutic Targeting of CD47 on Human Leukemia and Other Cancer Stem CellsP01CA139490 · NCI · STANFORD UNIVERSITY · PI CLARKE, MICHAEL · 2009 to 2013
$8.7M
Molecular and Functional Characterization of Colon Tumor Cancer Stem Cells and StU54CA126524 · NCI · STANFORD UNIVERSITY · PI TIBSHIRANI, ROB · 2006 to 2010
$5.6M
Self-Renewal of Normal and Leukemic Stem CellsR01CA100225 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CLARKE, MICHAEL · 2004 to 2015
$2.9M
ANALYSIS OF LEUKEMIA CELLSR01CA104987 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CLARKE, MICHAEL · 2004 to 2006
$933k
NCI NIH HHS CA100225NCI NIH HHS CA104987NCI NIH HHS CA126524NCI NIH HHS CA139490NCI NIH HHS P01 CA139490NCI NIH HHS R01 CA100225NCI NIH HHS R01 CA104987NCI NIH HHS U54 CA126524NCRR NIH HHS 1S10RR02933801
6 · The paper itself

Abstract

MicroRNAs (miRNAs) are important regulators of stem and progenitor cell functions. We previously reported that miR-142 and miR-150 are upregulated in human breast cancer stem cells (BCSCs) as compared to the non-tumorigenic breast cancer cells. In this study, we report that miR-142 efficiently recruits the APC mRNA to an RNA-induced silencing complex, activates the canonical WNT signaling pathway in an APC-suppression dependent manner, and activates the expression of miR-150. Enforced expression of miR-142 or miR-150 in normal mouse mammary stem cells resulted in the regeneration of hyperproliferative mammary glands in vivo. Knockdown of endogenous miR-142 effectively suppressed organoid formation by BCSCs and slowed tumor growth initiated by human BCSCs in vivo. These results suggest that in some tumors, miR-142 regulates the properties of BCSCs at least in part by activating the WNT signaling pathway and miR-150 expression.

Indexed as

Wnt Signaling PathwayAdenomatous Polyposis Coli ProteinAnimalsArgonaute ProteinsBase SequenceBreast NeoplasmsCarcinogenesisCell ProliferationClone CellsFemaleGene Expression Regulation, NeoplasticHumansHyperplasiaMammary Glands, AnimalMiceMicroRNAsAdenomatous Polyposis Coli ProteinAPC protein, humanArgonaute ProteinsMicroRNAsMIR150, humanMIRN142 microRNA, humanRNA-Induced Silencing ComplexRNA, MessengerAPCbreast cancercancer stem cellscell biologyhumanhuman biologymedicinemiR-142miR-150mouseWNT signaling pathway

Identifiers

PMID25406066
PMCPMC4235011

What OpenQuestion holds

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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.