Evidence map›Paper›PMID 25901191›Full record

ReviewAmerican journal of translational research2015

Cytokine networking of chondrocyte dedifferentiation in vitro and its implications for cell-based cartilage therapy.

Li Duan, Bin Ma, Yujie Liang, Jielin Chen, Weimin Zhu, Mingtao Li, Daping Wang

Open access · greenAbstract readReview
In one paragraph

Review in American journal of translational research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
6.2field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 73 citations in OpenAlex.

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  15. [Research progress of different cell seeding densities and cell ratios in cartilage tissue engineering].Zhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2022
    Review
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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 2 institutions in 1 country.

Li DuanSchool of Medicine, Sun Yat-sen University Guangzhou 510182, Guangdong Province, China ; Shenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China ; Department of Orthopedics, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China.
Bin MaDivision of Immunology, University Children's Hospital Zurich Zurich 8032, Switzerland.
Yujie LiangSchool of Chemical Biology & Biotechnology, Peking University Shenzhen Graduate School Shenzhen 518055, Guangdong Province, China.
Jielin ChenSchool of Medicine, Sun Yat-sen University Guangzhou 510182, Guangdong Province, China ; Shenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China ; Department of Orthopedics, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China.
Weimin ZhuShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China ; Department of Orthopedics, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China.
Mingtao LiSchool of Medicine, Sun Yat-sen University Guangzhou 510182, Guangdong Province, China.
Daping WangShenzhen Key Laboratory of Tissue Engineering, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China ; Department of Orthopedics, Shenzhen Second People's Hospital Shenzhen 518035, Guangdong Province, China.
Sun Yat-sen University · CNPeking University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Autologous chondrocyte implantation (ACI) is a golden treatment for large defects of the knee joint without osteoarthritis or other complications. Despite notable progresses, generation of a stable chondrocyte phenotype using progenitor cells remains a main obstacle for chondrocyte-based cartilage treatment. Monolayer chondrocyte expansion in vitro is accompanied by chondrocyte dedifferentiation, which produces a non-specific mechanically inferior extracellular matrix (ECM) unsuitable for ACI. In-depth understanding of the molecular events during chondrocyte dedifferentiation is required to maintain the capacity of in vitro expanded chondrocytes to produce hyaline cartilage-specific ECM. This review discusses key cytokines and signaling pathways involved in chondrocyte dedifferentiation from the standpoint of catabolism and anabolism. Some potential therapeutic strategies are also presented to counteract chondrocyte dedifferentiation for cell-based cartilage therapy.

Indexed as

autologous chondrocyte implantationcartilage repairChondrocyte dedifferentiationcytokinesin vitrosignaling pathways

Identifiers

PMID25901191
PMCPMC4399086
OpenAlexW2411087228

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.