Evidence map›Paper›PMID 22068423›Full record

ArticleMolecular therapy : the journal of the American Society of Gene Therapy2012

N-cadherin determines individual variations in the therapeutic efficacy of human umbilical cord blood-derived mesenchymal stem cells in a rat model of myocardial infarction.

Eun Ju Lee, Eue-Keun Choi, Soo Kyoung Kang, Gi-Hwan Kim, Ju Young Park, Hyun-Jae Kang, Sae-Won Lee, Keum-Hyun Kim, Jin Sook Kwon, Ki Hong Lee and 7 more

Open access · hybridAbstract read
In one paragraph

Article in Molecular therapy : the journal of the American Society of Gene Therapy, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing 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

29 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. N-CADHERINStem cell research & therapy · 2024
    Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. hPSC gene editing for cardiac disease therapy.Pflugers Archiv : European journal of physiology · 2022
    Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Hepatocyte Growth Factor Improves the Therapeutic Efficacy of Human Bone Marrow Mesenchymal Stem Cells via RAD51.Molecular therapy : the journal of the American Society of Gene Therapy · 2018
    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

17 authors at 4 institutions in 1 country.

Eun Ju LeeNational Research Laboratory for Cardiovascular Stem Cells and IRICT, Seoul National University Hospital, Seoul, Korea.
Eue-Keun Choi
Soo Kyoung Kang
Gi-Hwan Kim
Ju Young Park
Hyun-Jae Kang
Sae-Won Lee
Keum-Hyun Kim
Jin Sook Kwon
Ki Hong Lee
Youngkeun Ahn
Ho-Jae Lee
Hyun-Jai Cho
Soo Jin Choi
Won Il Oh
Young-Bae Park
Hyo-Soo Kim
Seoul National University Hospital · KRChonnam National University Hospital · KRSeoul National University · KRMedipost (South Korea) · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this study, we established and characterized human umbilical cord blood-derived mesenchymal stem cells (hUCB-MSCs) from four different donors. However, the hUCB-MSCs showed remarkable variations in their therapeutic efficacy for repairing rat infarcted myocardium (including the process of angiogenesis) 8 weeks after transplantation. In addition, we observed that the level of vascular endothelial growth factor (VEGF) is correlated with the therapeutic efficacy of the four hUCB-MSCs. Next, to investigate the practical application of hUCB-MSCs, we searched for surface signature molecules that could serve as indicators of therapeutic efficacy. The gene for N-cadherin was the only cell surface gene that was highly expressed in the most effective hUCB-MSCs, both at the transcriptional and translational levels. We observed downregulation and upregulation of VEGF in response to N-cadherin blocking and N-cadherin overexpression, respectively. Activation of extracellular signal-regulated kinase (ERK), but not protein kinase B, was increased when N-cadherin expression was increased, whereas disruption of N-cadherin-mediated cell-cell contact induced suppression of ERK activation and led to VEGF downregulation. Moreover, by investigating hUCB-MSCs overexpressing N-cadherin or N-cadherin knockdown hUCB-MSCs, we confirmed the in vivo function of N-cadherin. In addition, we observed that DiI-labeled hUCB-MSCs express N-cadherin in the peri-infarct area and interact with cardiomyocytes.

Indexed as

Cord Blood Stem Cell TransplantationMesenchymal Stem Cell TransplantationAnimalsBiomarkersCadherinsCell CommunicationDisease Models, AnimalExtracellular Signal-Regulated MAP KinasesFetal BloodGene Expression ProfilingHeartHumansImmunophenotypingMaleMesenchymal Stem CellsMyocardial InfarctionBiomarkersCadherinsExtracellular Signal-Regulated MAP KinasesVascular Endothelial Growth Factor A

Identifiers

PMID22068423
PMCPMC3255601
OpenAlexW2044294389

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.