Evidence map›Paper›PMID 23893300›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2013

MicroRNA-126-mediated control of cell fate in B-cell myeloid progenitors as a potential alternative to transcriptional factors.

Kazuki Okuyama, Tomokatsu Ikawa, Bernhard Gentner, Katsuto Hozumi, Ratanakanit Harnprasopwat, Jun Lu, Riu Yamashita, Daon Ha, Takae Toyoshima, Bidisha Chanda and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 24% 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

19 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
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  12. Article
  13. ncRNAs in Type-2 Immunity.Non-coding RNA · 2020
    Review
  14. Article
  15. miRNAs in B Cell Development and Lymphomagenesis.Trends in molecular medicine · 2017
    Review
  16. Article
  17. Article
  18. Review
  19. Review
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 at 7 institutions in 3 countries.

Kazuki OkuyamaDivision of Hematological Malignancy, Regenerative Medical Science, Tokai University School of Medicine, Kanagawa 259-1193, Japan.
Tomokatsu Ikawa
Bernhard Gentner
Katsuto Hozumi
Ratanakanit Harnprasopwat
Jun Lu
Riu Yamashita
Daon Ha
Takae Toyoshima
Bidisha Chanda
Toyotaka Kawamata
Kazuaki Yokoyama
Shusheng Wang
Kiyoshi Ando
Harvey F Lodish
Arinobu Tojo
Hiroshi Kawamoto
Ai Kotani
Tokai University · JPTokyo University of Science · JPRIKEN Center for Integrative Medical Sciences · JPSan Raffaele University of Rome · ITTufts University · USTulane University · USWhitehead Institute for Biomedical Research · US

Funding

VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI MATTHEW G. VANDER HEIDEN · 1985 to 2026
$93.9M
MicroRNAs and hematopoietic differentiationR01DK068348 · NIDDK · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI LODISH, HARVEY F · 2004 to 2019
$8.3M
Regulation of Ocular Angiogenesis by microRNAsR01EY021862 · NEI · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, SHUSHENG · 2011 to 2021
$2.8M
NCI NIH HHS P30 CA014051NEI NIH HHS R01 EY021862NIDDK NIH HHS R01 DK068348
6 · The paper itself

Abstract

Lineage specification is thought to be largely regulated at the level of transcription, where lineage-specific transcription factors drive specific cell fates. MicroRNAs (miR), vital to many cell functions, act posttranscriptionally to decrease the expression of target mRNAs. MLL-AF4 acute lymphocytic leukemia exhibits both myeloid and B-cell surface markers, suggesting that the transformed cells are B-cell myeloid progenitor cells. Through gain- and loss-of-function experiments, we demonstrated that microRNA 126 (miR-126) drives B-cell myeloid biphenotypic leukemia differentiation toward B cells without changing expression of E2A immunoglobulin enhancer-binding factor E12/E47 (E2A), early B-cell factor 1 (EBF1), or paired box protein 5, which are critical transcription factors in B-lymphopoiesis. Similar induction of B-cell differentiation by miR-126 was observed in normal hematopoietic cells in vitro and in vivo in uncommitted murine c-Kit(+)Sca1(+)Lineage(-) cells, with insulin regulatory subunit-1 acting as a target of miR-126. Importantly, in EBF1-deficient hematopoietic progenitor cells, which fail to differentiate into B cells, miR-126 significantly up-regulated B220, and induced the expression of B-cell genes, including recombination activating genes-1/2 and CD79a/b. These data suggest that miR-126 can at least partly rescue B-cell development independently of EBF1. These experiments show that miR-126 regulates myeloid vs. B-cell fate through an alternative machinery, establishing the critical role of miRNAs in the lineage specification of multipotent mammalian cells.

Indexed as

Gene Expression ProfilingAnalysis of VarianceBlotting, WesternB-LymphocytesBone Marrow TransplantationCell LineageCell Line, TumorDNA PrimersGenetic VectorsHumansLeukemia, B-CellLuciferasesMicroRNAsMyeloid Progenitor CellsOligonucleotidesStatistics, NonparametricDNA PrimersEBF1 protein, humanLuciferasesMicroRNAsMIRN126 microRNA, mouseOligonucleotidesTrans-ActivatorsTranscription Factor 3cell fate decisionlymphopoiesis

Identifiers

PMID23893300
PMCPMC3746909
OpenAlexW2069168290

What OpenQuestion holds

Textmetadata
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.