Evidence map›Paper›PMID 26000333›Full record

ArticleGenes & diseases2015

Strategies to minimize hypertrophy in cartilage engineering and regeneration.

Song Chen, Peiliang Fu, Ruijun Cong, HaiShan Wu, Ming Pei

Open access · diamondAbstract read
In one paragraph

Article in Genes & diseases, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 71 papers.

0numbers the graph read from it
0cells of the map it votes in
71citing papers in PubMed
14.2field-weighted citation impact, top 1% 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

71 citing papers in PubMed, 152 citations in OpenAlex.

  1. Article
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  8. Article
  9. Mesenchymal Stromal Cells for Aging Cartilage Regeneration: A Review.International journal of molecular sciences · 2024
    Review
  10. Article
  11. Review
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Suppressing Chondrocyte Hypertrophy to Build Better Cartilage.Bioengineering (Basel, Switzerland) · 2023
    Review
  20. Review

11 more citing papers are in PubMed but not listed here.

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

5 authors at 4 institutions in 2 countries.

Song ChenStem Cell and Tissue Engineering Laboratory, Department of Orthopaedics, West Virginia University, Morgantown, West Virginia 26506, USA ; Department of Joint Surgery, Shanghai Changzheng Hospital, The Second Military Medical University, Shanghai 200003, China.
Peiliang FuDepartment of Joint Surgery, Shanghai Changzheng Hospital, The Second Military Medical University, Shanghai 200003, China.
Ruijun CongDepartment of Orthopaedics, The 10th People's Hospital of Shanghai, Affiliated with Tongji University, Shanghai, 200072, China.
HaiShan WuDepartment of Joint Surgery, Shanghai Changzheng Hospital, The Second Military Medical University, Shanghai 200003, China.
Ming PeiStem Cell and Tissue Engineering Laboratory, Department of Orthopaedics, West Virginia University, Morgantown, West Virginia 26506, USA ; Exercise Physiology, West Virginia University, Morgantown, West Virginia 26506, USA ; Mechanical and Aerospace Engineering, West Virginia University, Morgantown, West Virginia 26506, USA.
West Virginia University · USSecond Military Medical University · CNShanghai Changzheng Hospital · CNTongji University · CN

Funding

Decellularized Matrix and Cartilage RegenerationR01AR067747 · NIAMS · WEST VIRGINIA UNIVERSITY · PI PEI, MING · 2016 to 2020
$1.7M
Decellularized Stem Cell Matrix Rejuvenates Human Cells from Herniated DiscsR03AR062763 · NIAMS · WEST VIRGINIA UNIVERSITY · PI PEI, MING · 2013 to 2015
$222k
NIAMS NIH HHS R01 AR067747NIAMS NIH HHS R03 AR062763
6 · The paper itself

Abstract

Due to a blood supply shortage, articular cartilage has a limited capacity for self-healing once damaged. Articular chondrocytes, cartilage progenitor cells, embryonic stem cells, and mesenchymal stem cells are candidate cells for cartilage regeneration. Significant current attention is paid to improving chondrogenic differentiation capacity; unfortunately, the potential chondrogenic hypertrophy of differentiated cells is largely overlooked. Consequently, the engineered tissue is actually a transient cartilage rather than a permanent one. The development of hypertrophic cartilage ends with the onset of endochondral bone formation which has inferior mechanical properties. In this review, current strategies for inhibition of chondrogenic hypertrophy are comprehensively summarized; the impact of cell source options is discussed; and potential mechanisms underlying these strategies are also categorized. This paper aims to provide guidelines for the prevention of hypertrophy in the regeneration of cartilage tissue. This knowledge may also facilitate the retardation of osteophytes in the treatment of osteoarthritis.

Indexed as

Adult stem cellCartilage regenerationCartilage repairCartilage tissue engineeringChondrogenesisHypertrophy

Identifiers

PMID26000333
PMCPMC4437543
OpenAlexW2022558287

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.