Evidence map›Paper›PMID 28864934›Full record

ReviewCellular and molecular life sciences : CMLS2018

Gene therapy for chondral and osteochondral regeneration: is the future now?

Daniele Bellavia, F Veronesi, V Carina, V Costa, L Raimondi, A De Luca, R Alessandro, M Fini, G Giavaresi

Open access · greenAbstract readReview
In one paragraph

Review in Cellular and molecular life sciences : CMLS, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
4.9field-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

32 citing papers in PubMed, 46 citations in OpenAlex.

  1. Review
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  8. Article
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  13. Advanced injectable hydrogels for cartilage tissue engineering.Frontiers in bioengineering and biotechnology · 2022
    Review
  14. A Review of the Use of Microparticles for Cartilage Tissue Engineering.International journal of molecular sciences · 2021
    Review
  15. Review
  16. Review
  17. Article
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  20. Emerging Gene-Editing Modalities for Osteoarthritis.International journal of molecular sciences · 2020
    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

9 authors at 2 institutions in 2 countries.

Daniele BellaviaRizzoli Orthopedic Institute, Bologna, Italy. daniele.bellavia@ior.it.ORCID 0000-0003-3308-9112
F VeronesiLaboratory of Preclinical and Surgical Studies, Rizzoli Orthopaedic Institute, Bologna, Italy.
V CarinaRizzoli Orthopedic Institute, Bologna, Italy.
V CostaRizzoli Orthopedic Institute, Bologna, Italy.
L RaimondiRizzoli Orthopedic Institute, Bologna, Italy.
A De LucaRizzoli Orthopedic Institute, Bologna, Italy.
R AlessandroBiology and Genetics Unit, Department of Biopathology and Medical Biotechnology, University of Palermo, Palermo, Italy.
M FiniLaboratory of Preclinical and Surgical Studies, Rizzoli Orthopaedic Institute, Bologna, Italy.
G GiavaresiInnovative Technology Platforms for Tissue Engineering, Theranostic and Oncology, Rizzoli Orthopaedic Institute, Via Divisi 83, 90133, Palermo, Italy.
Istituto Ortopedico Rizzoli · ITUniversity of Palermo · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gene therapy might represent a promising strategy for chondral and osteochondral defects repair by balancing the management of temporary joint mechanical incompetence with altered metabolic and inflammatory homeostasis. This review analysed preclinical and clinical studies on gene therapy for the repair of articular cartilage defects performed over the last 10 years, focussing on expression vectors (non-viral and viral), type of genes delivered and gene therapy procedures (direct or indirect). Plasmids (non-viral expression vectors) and adenovirus (viral vectors) were the most employed vectors in preclinical studies. Genes delivered encoded mainly for growth factors, followed by transcription factors, anti-inflammatory cytokines and, less frequently, by cell signalling proteins, matrix proteins and receptors. Direct injection of the expression vector was used less than indirect injection of cells, with or without scaffolds, transduced with genes of interest and then implanted into the lesion site. Clinical trials (phases I, II or III) on safety, biological activity, efficacy, toxicity or bio-distribution employed adenovirus viral vectors to deliver growth factors or anti-inflammatory cytokines, for the treatment of osteoarthritis or degenerative arthritis, and tumour necrosis factor receptor or interferon for the treatment of inflammatory arthritis.

Indexed as

Genetic TherapyAnimalsBone RegenerationCartilage, ArticularChondrocytesHumansOsteoarthritisRegenerationCartilage repairExpression vectorsGene therapy proceduresOsteoarthritisRegenerative medicine

Identifiers

PMID28864934
PMCPMC11105387
OpenAlexW2752784971

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.