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Journal ArticleDOI

Bone morphogenetic proteins in clinical applications.

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TLDR
The purpose of this paper is to give a brief overview of BMPs and to critically review the clinical data currently available on the use of B MP‐2 and BMP‐7 in fracture healing.
Abstract
The role of bone morphogenetic proteins (BMPs) in bone healing has been shown in numerous animal models. To date, at least 20 BMPs have been identified, some of which have been shown in vitro to stimulate the process of stem cell differentiation into osteoblasts in human and animal models. Having realized the osteoinductive properties of BMPs and having identified their genetic sequences, recombinant gene technology has been used to produce BMPs for clinical application - most commonly, as alternatives or adjuncts in the treatment of cases in which fracture healing is compromised. BMP-2 and BMP-7 are approved for clinical use in open fractures of long bones, non-unions and spinal fusion. However, despite significant evidence of their potential benefit to bone repair and regeneration in animal and preclinical studies, there is, to date, a dearth of convincing clinical trials. The purpose of this paper is to give a brief overview of BMPs and to critically review the clinical data currently available on the use of BMP-2 and BMP-7 in fracture healing.

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Cancer to bone: a fatal attraction

TL;DR: Understanding the crucial components of the bone microenvironment that influence tumour localization, along with the tumour-derived factors that modulate cellular and protein matrix components of bone to favour tumour expansion and invasion, is central to the pathophysiology of bone metastases.
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BMP signalling in skeletal development, disease and repair

TL;DR: The genetic evidence implicating BMP superfamily signalling in vertebrate bone and joint development is examined, a selection of human skeletal disorders associated with altered BMP signalling is discussed, and the status of modulating the BMP pathway as a therapeutic target for skeletal trauma and disease is summarized.
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Bone morphogenetic proteins in tissue engineering: the road from laboratory to clinic, part II (BMP delivery)

TL;DR: There are prospects of a brilliant future in the field of regenerative medicine of bone and cartilage with the use of BMPs, according to the expanding number of publications.
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Engineering the Growth Factor Microenvironment with Fibronectin Domains to Promote Wound and Bone Tissue Healing

TL;DR: Preclinical demonstrations in rodent models show promise for the use of the FN III9-10/12-14–modified matrices in humans to heal chronic wounds and repair bones, and shows potent synergistic signaling and morphogenesis between α5β1 integrin and the growth factor receptors.
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Engineering the regenerative microenvironment with biomaterials.

TL;DR: Important aspects of the healing microenvironment, and how these features can be incorporated within innovative hydrogel scaffolds, are presented.
References
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Journal ArticleDOI

Bone: Formation by Autoinduction

TL;DR: Differentiation of the osteoprogenitor cell is elicited by local alterations in cell metabolic cycles that are as yet uncharacterized and may transfer collagenolytic activity to the substrate to cause dissolution of the matrix.
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TL;DR: Differentiation of the osteoprogenitor cell is elicited by local alterations in cell metabolic cycles that are as yet uncharacterized and may transfer collagenolytic activity to the substrate to cause dissolution of the matrix.
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Modulation of osteoclast differentiation and function by the new members of the tumor necrosis factor receptor and ligand families.

TL;DR: Osteoblasts/stromal cells can now be replaced with RANKL and M-CSF in dealing with the whole life of osteoclasts, and new ways to treat several metabolic bone diseases caused by abnormal osteoclast recruitment and functions will be established.
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Recombinant human bone morphogenetic protein-2 for treatment of open tibial fractures a prospective, controlled, randomized study of four hundred and fifty patients

TL;DR: The rhBMP-2 implant was safe and, when 1.50 mg/mL was used, significantly superior to the standard of care in reducing the frequency of secondary interventions and the overall invasiveness of the procedures, accelerating fracture and wound-healing, and reducing the infection rate in patients with an open fracture of the tibia.
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