Evidence map›Paper›PMID 24038734›Full record

ArticleStem cells (Dayton, Ohio)2014

Genome-wide analysis of miRNA-mRNA interactions in marrow stromal cells.

Ilango Balakrishnan, Xiaodong Yang, Joseph Brown, Aravind Ramakrishnan, Beverly Torok-Storb, Peter Kabos, Jay R Hesselberth, Manoj M Pillai

Open access · bronzeAbstract read
In one paragraph

Article in Stem cells (Dayton, Ohio), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed, 3 pooled it
2.3field-weighted citation impact, top 12% 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

55 citing papers in PubMed, 3 syntheses or guidelines pooled it, 81 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
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  6. Review
  7. Article
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  12. Effects of hsa-miR-9-3p and hsa-miR-9-5p on Topoisomerase IIThe Journal of pharmacology and experimental therapeutics · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Upregulated miRNAs on theFrontiers in genetics · 2022
    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

8 authors at 2 institutions in 1 country.

Ilango BalakrishnanDepartment of Medicine, University of Colorado Denver, Aurora, Colorado, USA.
Xiaodong Yang
Joseph Brown
Aravind Ramakrishnan
Beverly Torok-Storb
Peter Kabos
Jay R Hesselberth
Manoj M Pillai
University of Colorado Denver · USFred Hutch Cancer Center · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Safety &Efficacy of Intravas. Del. of AAV-F.IX to Skeletal MuscleP01HL064190 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI PONCZ, MORTIMER · 2000 to 2015
$27.8M
Protein CoreP01HL110860 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI RAUOVA, LUBICA · 2012 to 2016
$11.4M
Embryonic Stem Cell-Derived Platelets as Cellular TherapeuticsU01HL099656 · NHLBI · CHILDREN'S HOSP OF PHILADELPHIA · PI PONCZ, MORTIMER · 2009 to 2015
$8.6M
Controlling Hematopoietic Lineage Commitment from ESC to PlateletsU01HL099993 · NHLBI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI TOROK-STORB, BEVERLY J. · 2009 to 2015
$8.3M
PROGESTERONE RECEPTOR INTERACTIONR01CA046938 · NCI · UNIVERSITY OF COLORADO DENVER · PI EDWARDS, DEAN P · 1988 to 2013
$3.3M
Role of microRNAs in regulation of the marrow microenvironmentR01HL104070 · NHLBI · YALE UNIVERSITY · PI PILLAI, MANOJ M. · 2011 to 2015
$2.2M
Regulation of anti-endocrine resistance of breast cancer by a network of non-codiK08CA164048 · NCI · UNIVERSITY OF COLORADO DENVER · PI KABOS, PETER · 2012 to 2016
$859k
Generating iPS cells by reprogramming using small moleculesK08DK082783 · NIDDK · FRED HUTCHINSON CANCER RESEARCH CENTER · PI RAMAKRISHNAN, ARAVIND · 2009 to 2013
$671k
Monocyte derived CXCL7 in the marrow microenvironmentK08DK073701 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI PILLAI, MANOJ M. · 2006 to 2010
$641k
Role of macrophages in MSC-mediated recovery of hematopoiesis after irradiationR03DK082757 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI PILLAI, MANOJ M. · 2009 to 2010
$137k
NCI NIH HHS CA164048NCI NIH HHS K08 CA164048NCI NIH HHS P30 CA046934NCI NIH HHS P30CA046934NCI NIH HHS R01 CA046938NHLBI NIH HHS HL099993NHLBI NIH HHS HL104070NHLBI NIH HHS P01 HL064190NHLBI NIH HHS P01 HL110860NHLBI NIH HHS R01 HL104070NHLBI NIH HHS U01 HL099656NHLBI NIH HHS U01 HL099993NIDDK NIH HHS DK073701NIDDK NIH HHS DK082783NIDDK NIH HHS K08 DK073701NIDDK NIH HHS K08 DK082783NIDDK NIH HHS R03 DK082757
6 · The paper itself

Abstract

Regulation of hematopoietic stem cell proliferation, lineage commitment, and differentiation in adult vertebrates requires extrinsic signals provided by cells in the marrow microenvironment (ME) located within the bone marrow. Both secreted and cell-surface bound factors critical to this regulation have been identified, yet control of their expression by cells within the ME has not been addressed. Herein we hypothesize that microRNAs (miRNAs) contribute to their controlled expression. MiRNAs are small noncoding RNAs that bind to target mRNAs and downregulate gene expression by either initiating mRNA degradation or preventing peptide translation. Testing the role of miRNAs in downregulating gene expression has been difficult since conventional techniques used to define miRNA-mRNA interactions are indirect and have high false-positive and negative rates. In this report, a genome-wide biochemical technique (high-throughput sequencing of RNA isolated by cross-linking immunoprecipitation or HITS-CLIP) was used to generate unbiased genome-wide maps of miRNA-mRNA interactions in two critical cellular components of the marrow ME: marrow stromal cells and bone marrow endothelial cells. Analysis of these datasets identified miRNAs as direct regulators of JAG1, WNT5A, MMP2, and VEGFA; four factors that are important to ME function. Our results show the feasibility and utility of unbiased genome-wide biochemical techniques in dissecting the role of miRNAs in regulation of complex tissues such as the marrow ME.

Indexed as

Argonaute ProteinsBase SequenceBone Marrow CellsCalcium-Binding ProteinsCell LineCellular MicroenvironmentDown-RegulationEndothelial CellsGenome, HumanHigh-Throughput Nucleotide SequencingHumansImmunoprecipitationIntercellular Signaling Peptides and ProteinsJagged-1 ProteinMatrix Metalloproteinase 2Membrane ProteinsArgonaute ProteinsCalcium-Binding ProteinsIntercellular Signaling Peptides and ProteinsJAG1 protein, humanJagged-1 ProteinMatrix Metalloproteinase 2Membrane ProteinsMicroRNAsProto-Oncogene ProteinsRNA, MessengerSerrate-Jagged ProteinsVascular Endothelial Growth Factor AWnt-5a ProteinWNT5A protein, humanWnt ProteinsBone marrow stromal cellsEndotheliumJAG1Mesenchymal stromal cellsmiRNAMMP2Stem cell microenvironmentVEGFAWNT5A

Identifiers

PMID24038734
PMCPMC4127404
OpenAlexW1518330963

What OpenQuestion holds

Textmetadata
LicenceTDM
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.