Evidence map›Paper›PMID 20212066›Full record

ArticleThe Journal of experimental medicine2010

microRNA-29a induces aberrant self-renewal capacity in hematopoietic progenitors, biased myeloid development, and acute myeloid leukemia.

Yoon-Chi Han, Christopher Y Park, Govind Bhagat, Jinping Zhang, Yulei Wang, Jian-Bing Fan, Mofang Liu, Yongrui Zou, Irving L Weissman, Hua Gu

Registry-linked trialOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01927354 (Observational Study on the Investigation of the Molecular Mechanism and Clinical Significance of the Interplay Between Twist1 and Other EMT Regulators Through microRNA-29 Family.), which is not on this map. Cited by 170 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
170citing papers in PubMed, 1 pooled it
12.2field-weighted citation impact, top 1% 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.

NCT01927354 unknown statusnot on this mapstarted 2012, after this paper: background citation

Observational Study on the Investigation of the Molecular Mechanism and Clinical Significance of the Interplay Between Twist1 and Other EMT Regulators Through microRNA-29 Family.

TypeobservationalSponsorNational Taiwan University HospitalRan2012 to 2014Enrolled100ConditionsHead-and-Neck Squamous Cell Carcinoma
3 · Its place in the literature

Who cites it

170 citing papers in PubMed, 1 synthesis or guideline pooled it, 289 citations in OpenAlex.

  1. Pooled it
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  15. CPT1B, a metabolic molecule, is also an independent risk factor in CN-AML.Cancer biomarkers : section A of Disease markers · 2023
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110 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

10 authors at 5 institutions in 2 countries.

Yoon-Chi HanDepartment of Microbiology and Immunology, Columbia University College of Physicians and Surgeons, New York, NY 10032, USA.
Christopher Y Park
Govind Bhagat
Jinping Zhang
Yulei Wang
Jian-Bing Fan
Mofang Liu
Yongrui Zou
Irving L Weissman
Hua Gu
Columbia University · USCalifornia Institute for Regenerative Medicine · USChinese Academy of Sciences · CNFeinstein Institute for Medical Research · USIllumina (United States) · US

Funding

HSC Diversity: Regulation by Clonal Selection vs Epigenetic InductionR01CA086065 · NCI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2000 to 2017
$6.9M
MOLECULAR CHARACTERIZATION OF ACUTE MYELOID LEUKEMIAR01CA086017 · NCI · STANFORD UNIVERSITY · PI WEISSMAN, IRVING L. · 2000 to 2015
$5.5M
IMMUNOLOGICAL DISEASE MECHANISMST32AI007525 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GHOSH, SANKAR · 1997 to 2006
$2.3M
NCI NIH HHS K08 CA1295470NCI NIH HHS R01 CA086017NCI NIH HHS R01 CA086065NCI NIH HHS R01 CA86017NIAID NIH HHS AI07525NIAID NIH HHS T32 AI007525
6 · The paper itself

Abstract

The function of microRNAs (miRNAs) in hematopoietic stem cells (HSCs), committed progenitors, and leukemia stem cells (LSCs) is poorly understood. We show that miR-29a is highly expressed in HSC and down-regulated in hematopoietic progenitors. Ectopic expression of miR-29a in mouse HSC/progenitors results in acquisition of self-renewal capacity by myeloid progenitors, biased myeloid differentiation, and the development of a myeloproliferative disorder that progresses to acute myeloid leukemia (AML). miR-29a promotes progenitor proliferation by expediting G1 to S/G2 cell cycle transitions. miR-29a is overexpressed in human AML and, like human LSC, miR-29a-expressing myeloid progenitors serially transplant AML. Our data indicate that miR-29a regulates early hematopoiesis and suggest that miR-29a initiates AML by converting myeloid progenitors into self-renewing LSC.

Indexed as

AnimalsCell CycleCell DivisionGene Expression RegulationHematopoiesisHematopoietic Stem CellsHumansLeukemia, Myeloid, AcuteMiceMicroRNAsMyeloid CellsMyeloproliferative DisordersStem CellsMicroRNAsMIRN29a microRNA, human

Identifiers

PMID20212066
PMCPMC2839143
OpenAlexW2149784145

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
Read underepoch 390

Registered trials

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.