Evidence map›Paper›PMID 27150539›Full record

ArticleStem cell research & therapy2016

Chm-1 gene-modified bone marrow mesenchymal stem cells maintain the chondrogenic phenotype of tissue-engineered cartilage.

Zhuoyue Chen, Jing Wei, Jun Zhu, Wei Liu, Jihong Cui, Hongmin Li, Fulin Chen

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Chondromodulin-1 in health, osteoarthritis, cancer, and heart disease.Cellular and molecular life sciences : CMLS · 2019
    Review
  11. Article
  12. Article
  13. Article
  14. 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

7 authors at 1 institution in 1 country.

Zhuoyue ChenLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China.
Jing WeiLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China.
Jun ZhuLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China.
Wei LiuLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China.
Jihong CuiLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China.
Hongmin LiLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China.
Fulin ChenLaboratory of Tissue Engineering, Faculty of Life Science, Northwest University, 229 TaiBai North Road, Xi'an, Shaanxi Province, 710069, P.R. China. chenfl@nwu.edu.cn.
Northwest University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMarrow mesenchymal stem cells (MSCs) can differentiate into specific phenotypes, including chondrocytes, and have been widely used for cartilage tissue engineering. However, cartilage grafts from MSCs exhibit phenotypic alternations after implantation, including matrix calcification and vascular ingrowth.

methodsWe compared chondromodulin-1 (Chm-1) expression between chondrocytes and MSCs. We found that chondrocytes expressed a high level of Chm-1. We then adenovirally transduced MSCs with Chm-1 and applied modified cells to engineer cartilage in vivo.

resultsA gross inspection and histological observation indicated that the chondrogenic phenotype of the tissue-engineered cartilage graft was well maintained, and the stable expression of Chm-1 was detected by immunohistological staining in the cartilage graft derived from the Chm-1 gene-modified MSCs.

conclusionsOur findings defined an essential role for Chm-1 in maintaining chondrogenic phenotype and demonstrated that Chm-1 gene-modified MSCs may be used in cartilage tissue engineering.

Indexed as

Mesenchymal Stem Cell TransplantationAnimalsAnthozoaBone Marrow CellsCartilageCell DifferentiationChemotactic FactorsChondrocytesChondrogenesisGene ExpressionGraft SurvivalMesenchymal Stem CellsPorosityPrimary Cell CultureRabbitsTissue EngineeringChemotactic FactorsCartilage tissueChondrocytesChondromodulin-1Mesenchymal stem cells

Identifiers

PMID27150539
PMCPMC4858869
OpenAlexW2346941603

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.