Evidence map›Paper›PMID 21671060›Full record

ArticleStem cell reviews and reports2012

Functional and transcriptomic recovery of infarcted mouse myocardium treated with bone marrow mononuclear cells.

Stephan Lachtermacher, Bruno L B Esporcatte, Fábio da Silva de Azevedo Fortes, Nazareth Novaes Rocha, Fabrício Montalvão, Patricia C Costa, Luciano Belem, Arnaldo Rabischoffisky, Hugo C C Faria Neto, Rita Vasconcellos and 6 more

Abstract read
In one paragraph

Article in Stem cell reviews and reports, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

16 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Powerful quantifiers for cancer transcriptomics.World journal of clinical oncology · 2020
    Review
  5. Article
  6. Article
  7. Tissue evacuated during joint replacement procedure as a source of mononuclear cells.European journal of orthopaedic surgery & traumatology : orthopedie traumatologie · 2018
    Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Plasticity of the myelination genomic fabric.Molecular genetics and genomics : MGG · 2012
    Article
  13. Article
  14. Article
  15. Article
  16. The Einstein-Brazil Fogarty: A decade of synergy.Brazilian journal of microbiology : [publication of the Brazilian Society for Microbiology]
    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

16 authors at 5 institutions in 2 countries.

Stephan LachtermacherInstituto de Biofísica Carlos Chagas Filho, Universidade Federal do Rio de Janeiro, Bloco G, Ilha do Fundão 21949-900, Rio de Janeiro, RJ, Brazil.
Bruno L B Esporcatte
Fábio da Silva de Azevedo Fortes
Nazareth Novaes Rocha
Fabrício Montalvão
Patricia C Costa
Luciano Belem
Arnaldo Rabischoffisky
Hugo C C Faria Neto
Rita Vasconcellos
Dumitru A Iacobas
Sanda Iacobas
David C Spray
Neil M Thomas
Regina C S Goldenberg
Antonio C Campos de Carvalho
Universidade Federal do Rio de Janeiro · BRAlbert Einstein College of Medicine · USHospital Pró-Cardíaco · BRUniversidade Federal Fluminense · BRFundação Oswaldo Cruz · BR

Funding

Stem Cell Based Therapies in Chagasic CardiomyopathyR01HL073732 · NHLBI · YESHIVA UNIVERSITY · PI CAMPOS DE CARVALHO, ANTONIO CARLOS · 2003 to 2011
$3.2M
"Connexin-Dependent Transcriptomic Networks in Controlling the Heart Rhythm"R01HL092001 · NHLBI · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI IACOBAS, DUMITRU ANDREI · 2009 to 2010
$830k
NHLBI NIH HHS R01 HL073732NHLBI NIH HHS R01 HL092001
6 · The paper itself

Abstract

Although bone marrow-derived mononuclear cells (BMNC) have been extensively used in cell therapy for cardiac diseases, little mechanistic information is available to support reports of their efficacy. To address this shortcoming, we compared structural and functional recovery and associated global gene expression profiles in post-ischaemic myocardium treated with BMNC transplantation. BMNC suspensions were injected into cardiac scar tissue 10 days after experimental myocardial infarction. Six weeks later, mice undergoing BMNC therapy were found to have normalized antibody repertoire and improved cardiac performance measured by ECG, treadmill exercise time and echocardiography. After functional testing, gene expression profiles in cardiac tissue were evaluated using high-density oligonucleotide arrays. Expression of more than 18% of the 11981 quantified unigenes was significantly altered in the infarcted hearts. BMNC therapy restored expression of 2099 (96.2%) of the genes that were altered by infarction but led to altered expression of 286 other genes, considered to be a side effect of the treatment. Transcriptional therapeutic efficacy, a metric calculated using a formula that incorporates both recovery and side effect of treatment, was 73%. In conclusion, our results confirm a beneficial role for bone marrow-derived cell therapy and provide new information on molecular mechanisms operating after BMNC transplantation on post ischemic heart failure in mice.

Indexed as

Bone Marrow TransplantationTranscriptomeAnimalsFemaleGene Expression ProfilingGene Expression RegulationHeartInflammation MediatorsMaleMiceMice, Inbred C57BLMyocardial InfarctionMyocardiumOligonucleotide Array Sequence AnalysisOxygen ConsumptionPhysical ExertionInflammation Mediators

Identifiers

PMID21671060
PMCPMC3212608
OpenAlexW2138157660

What OpenQuestion holds

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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.