Cited by 326Periodontal Regeneration and TreatmentsBone Tissue Engineering MaterialsTGF-β signaling in diseases

Bone Morphogenetic Proteins: Facts, Challenges, and Future Perspectives

Carreira, A.C., Lojudice, F.H., Halcsik, E., Navarro, R.D., Sogayar, M.C., Granjeiro, J.M.·2014·Journal of Dental Research

Abstract

Bone morphogenetic proteins (BMPs) are members of the TGF-β superfamily, acting as potent regulators during embryogenesis and bone and cartilage formation and repair. Cell and molecular biology approaches have unveiled the great complexity of BMP action, later confirmed by transgenic animal studies. Genetic engineering allows for the production of large amounts of BMPs for clinical use, but they have systematically been associated with a delivery system, such as type I collagen and calcium phosphate ceramics, to ensure controlled release and to maximize their biological activity at the surgical site, avoiding systemic diffusion. Clinical orthopedic studies have shown the benefits of FDA-approved recombinant human BMPs (rhBMPs) 2 and 7, but side effects, such as swelling, seroma, and increased cancer risk, have been reported, probably due to high BMP dosage. Several studies have supported the use of BMPs in periodontal regeneration, sinus lift bone-grafting, and non-unions in oral surgery. However, the clinical use of BMPs is growing mainly in off-label applications, with robust evidence to ascertain rhBMPs’ safety and efficacy through well-designed, randomized, and double-blind clinical trials. Here we review and discuss the critical data on BMP structure, mechanisms of action, and possible clinical applications.

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Crossref · 10.1177/0022034513518561

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1 of 1 references verified0 citation errors · 0 not checkable

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  • GDF10 is a divergent member of the bone morphogenetic protein (BMP)/transforming growth factor-β (TGFβ) superfamily.

    “GDF10 is a divergent member of the bone morphogenetic protein (BMP)/transforming growth factor-β (TGFβ) superfamily11–14”
  • The magnitude of post-stroke axonal sprouting induced by GDF10 exceeds that seen with the blockade of several axonal growth inhibitory systems, such as ephrin-A5 and Nogo/NgR.

    “The magnitude of post-stroke axonal sprouting induced by GDF10 exceeds that seen with the blockade of several axonal growth inhibitory systems, such as ephrin-A54 and Nogo/NgR13.”
  • Though TGF and GDF10 both signal through TGFβRI/II, their signaling levels are not equivalent.

    “Though TGF and GDF10 both signal through TGFβRI/II12–14, we show that their signaling levels are not equivalent.”

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Authors
Carreira, A. C., Lojudice, F. H., Halcsik, E., Navarro, R. D., Sogayar, M. C., & Granjeiro, J. M.
Affiliations
  • Universidade de São Paulo (BR)
  • Universidade Estadual de Maringá (BR)
  • Universidade Federal Fluminense (BR)
Corresponding author
Granjeiro, J.M.
Venue
Journal of Dental Research
Published
2014-01-03
Volume
93
Issue
4
Pages
335-345
ISSN
  • 0022-0345 (ISSN-L)
  • 1544-0591
OpenAlex
W2118089919
Cited by
326
References
1
Citations by year
2026: 8 · 2025: 22 · 2024: 22 · 2023: 22 · 2022: 21 · 2021: 30 · 2020: 30 · 2019: 24 · 2018: 31 · 2017: 35 · 2016: 45 · 2015: 26 · 2014: 10
FWCI
8.08
Type
journal article
Language
en
Open access
closed
Locations
  • Journal of Dental Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
Banco Nacional de Desenvolvimento Econômico e Social
Topics
  • Health Sciences › Medicine › Urology › Periodontal Regeneration and Treatments
  • Physical Sciences › Engineering › Biomedical Engineering › Bone Tissue Engineering Materials
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › TGF-β signaling in diseases
Keywords
bone morphogenetic proteins, TGF-beta superfamily, recombinant human BMP-2, bone regeneration, periodontal regeneration, maxillary sinus floor elevation, nonunion, bone grafting, controlled drug delivery, collagen scaffolds, calcium phosphate ceramics, off-label drug use
MeSH terms
Bone Regeneration, Humans, Osteogenesis, Recombinant Proteins, Structure-Activity Relationship, Signal Transduction, Transforming Growth Factor beta, Drug Delivery Systems, Bone Morphogenetic Proteins, Chondrogenesis, Bone Morphogenetic Protein 2, Bone Morphogenetic Protein 7

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