Diabetic Foot Ulcers and Epidermal Growth Factor: Revisiting the Local Delivery Route for a Successful Outcome
Soon after epidermal growth factor (EGF) discovery, some in vivo models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the first growth factor (GF) introduced in the clinical arena as a healing enhancer, exerting its mitogenic effects on epithelial, fibroblastoid, an...
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Published in: | BioMed research international Vol. 2017; no. 2017; pp. 1 - 10 |
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Main Authors: | , , , , , , , , , , , , , |
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Language: | English |
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Cairo, Egypt
Hindawi Publishing Corporation
01-01-2017
Hindawi John Wiley & Sons, Inc Hindawi Limited |
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Abstract | Soon after epidermal growth factor (EGF) discovery, some in vivo models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the first growth factor (GF) introduced in the clinical arena as a healing enhancer, exerting its mitogenic effects on epithelial, fibroblastoid, and endothelial cells via a tyrosine kinase membrane receptor. Compelling evidences from the 90s documented that, for EGF, locally prolonged bioavailability and hourly interaction with the receptor were necessary for a successful tissue response. Eventually, the enthusiasm on the clinical use of EGF to steer the healing process was wiped out as the topical route to deliver proteins started to be questioned. The simultaneous in vivo experiments, emphasizing the impact of the parenterally administered EGF on epithelial and nonepithelial organs in terms of mitogenesis and cytoprotection, rendered the theoretical fundamentals for the injectable use of EGF and shaped the hypothesis that locally infiltrating the diabetic ulcers would lead to an effective healing. Although the diabetic chronic wounds microenvironment is hostile for local GFs bioavailability, EGF local infiltration circumvented the limitations of its topical application, thus expanding its therapeutic prospect. Our clinical pharmacovigilance and basic studies attest the significance of the GF local infiltration for chronic wounds healing. |
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AbstractList | Soon after epidermal growth factor (EGF) discovery, some in vivo models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the first growth factor (GF) introduced in the clinical arena as a healing enhancer, exerting its mitogenic effects on epithelial, fibroblastoid, and endothelial cells via a tyrosine kinase membrane receptor. Compelling evidences from the 90s documented that, for EGF, locally prolonged bioavailability and hourly interaction with the receptor were necessary for a successful tissue response. Eventually, the enthusiasm on the clinical use of EGF to steer the healing process was wiped out as the topical route to deliver proteins started to be questioned. The simultaneous in vivo experiments, emphasizing the impact of the parenterally administered EGF on epithelial and nonepithelial organs in terms of mitogenesis and cytoprotection, rendered the theoretical fundamentals for the injectable use of EGF and shaped the hypothesis that locally infiltrating the diabetic ulcers would lead to an effective healing. Although the diabetic chronic wounds microenvironment is hostile for local GFs bioavailability, EGF local infiltration circumvented the limitations of its topical application, thus expanding its therapeutic prospect. Our clinical pharmacovigilance and basic studies attest the significance of the GF local infiltration for chronic wounds healing. Soon after epidermal growth factor (EGF) discovery, some in vivo models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the first growth factor (GF) introduced in the clinical arena as a healing enhancer, exerting its mitogenic effects on epithelial, fibroblastoid, and endothelial cells via a tyrosine kinase membrane receptor. Compelling evidences from the 90s documented that, for EGF, locally prolonged bioavailability and hourly interaction with the receptor were necessary for a successful tissue response. Eventually, the enthusiasm on the clinical use of EGF to steer the healing process was wiped out as the topical route to deliver proteins started to be questioned. The simultaneous in vivo experiments, emphasizing the impact of the parenterally administered EGF on epithelial and nonepithelial organs in terms of mitogenesis and cytoprotection, rendered the theoretical fundamentals for the injectable use of EGF and shaped the hypothesis that locally infiltrating the diabetic ulcers would lead to an effective healing. Although the diabetic chronic wounds microenvironment is hostile for local GFs bioavailability, EGF local infiltration circumvented the limitations of its topical application, thus expanding its therapeutic prospect. Our clinical pharmacovigilance and basic studies attest the significance of the GF local infiltration for chronic wounds healing. Soon after epidermal growth factor (EGF) discovery, some models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the first growth factor (GF) introduced in the clinical arena as a healing enhancer, exerting its mitogenic effects on epithelial, fibroblastoid, and endothelial cells via a tyrosine kinase membrane receptor. Compelling evidences from the 90s documented that, for EGF, locally prolonged bioavailability and hourly interaction with the receptor were necessary for a successful tissue response. Eventually, the enthusiasm on the clinical use of EGF to steer the healing process was wiped out as the topical route to deliver proteins started to be questioned. The simultaneous experiments, emphasizing the impact of the parenterally administered EGF on epithelial and nonepithelial organs in terms of mitogenesis and cytoprotection, rendered the theoretical fundamentals for the injectable use of EGF and shaped the hypothesis that locally infiltrating the diabetic ulcers would lead to an effective healing. Although the diabetic chronic wounds microenvironment is hostile for local GFs bioavailability, EGF local infiltration circumvented the limitations of its topical application, thus expanding its therapeutic prospect. Our clinical pharmacovigilance and basic studies attest the significance of the GF local infiltration for chronic wounds healing. |
Audience | Academic |
Author | Falcón‐Cama, Viviana Pérez-Saad, Héctor Mendoza-Marí, Yssel Valdés-Pérez, Calixto Kulikovsky, Moshe García del Barco Herrera, Diana Guillen Nieto, Gerardo E. Fernández-Mayola, Maday Pimentel-Vázquez, Eulogio Fernández-Montequín, José Berlanga-Acosta, Jorge Urquiza-Rodríguez, Aleida Savigne-Gutiérrez, William García-Ojalvo, Ariana |
AuthorAffiliation | 2 National Institute of Angiology and Vascular Surgery, Calzada del Cerro No. 1551, El Cerro, Havana, Cuba 1 Wound Healing and Cytoprotection Research Group, Center for Genetic Engineering and Biotechnology, Ave 31 e/158 and 190, Cubanacan, Playa, P.O. Box 10600, Havana, Cuba 3 Dermatology Department, Center for Surgical and Medical Research, Calle 216 y 11-B, Reparto Siboney, Playa, Havana, Cuba 4 Lin Medical Center, Rehov Vardia 12, 3465712 Haifa, Israel |
AuthorAffiliation_xml | – name: 3 Dermatology Department, Center for Surgical and Medical Research, Calle 216 y 11-B, Reparto Siboney, Playa, Havana, Cuba – name: 4 Lin Medical Center, Rehov Vardia 12, 3465712 Haifa, Israel – name: 1 Wound Healing and Cytoprotection Research Group, Center for Genetic Engineering and Biotechnology, Ave 31 e/158 and 190, Cubanacan, Playa, P.O. Box 10600, Havana, Cuba – name: 2 National Institute of Angiology and Vascular Surgery, Calzada del Cerro No. 1551, El Cerro, Havana, Cuba |
Author_xml | – sequence: 1 fullname: Fernández-Mayola, Maday – sequence: 2 fullname: Pimentel-Vázquez, Eulogio – sequence: 3 fullname: Urquiza-Rodríguez, Aleida – sequence: 4 fullname: Kulikovsky, Moshe – sequence: 5 fullname: Guillen Nieto, Gerardo E. – sequence: 6 fullname: García del Barco Herrera, Diana – sequence: 7 fullname: Falcón‐Cama, Viviana – sequence: 8 fullname: García-Ojalvo, Ariana – sequence: 9 fullname: Mendoza-Marí, Yssel – sequence: 10 fullname: Savigne-Gutiérrez, William – sequence: 11 fullname: Valdés-Pérez, Calixto – sequence: 12 fullname: Fernández-Montequín, José – sequence: 13 fullname: Berlanga-Acosta, Jorge – sequence: 14 fullname: Pérez-Saad, Héctor |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/28904951$$D View this record in MEDLINE/PubMed |
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ContentType | Journal Article |
Copyright | Copyright © 2017 Jorge Berlanga-Acosta et al. COPYRIGHT 2017 John Wiley & Sons, Inc. Copyright © 2017 Jorge Berlanga-Acosta et al.; This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright © 2017 Jorge Berlanga-Acosta et al. 2017 |
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Snippet | Soon after epidermal growth factor (EGF) discovery, some in vivo models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the... Soon after epidermal growth factor (EGF) discovery, some models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the first... Soon after epidermal growth factor (EGF) discovery, some in vivo models appeared demonstrating its property to enhance cutaneous wound healing. EGF was the... |
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SubjectTerms | Administration, Topical Amputation Analysis Angiogenesis Bioavailability Biochemistry Cellular Microenvironment - drug effects Diabetes Diabetes mellitus Diabetic foot Diabetic Foot - drug therapy Diabetic Foot - genetics Diabetic Foot - pathology Endothelial cells Epidermal growth factor Epidermal Growth Factor - genetics Epidermal Growth Factor - therapeutic use Epigenetics Feet Fibroblasts Foot diseases Health aspects Humans Hypoxia Infiltration Leg ulcers Methods Mortality Organs Peripheral neuropathy Pharmacology Pharmacovigilance Physiological aspects Physiology Protein-tyrosine kinase Proteins Receptor Protein-Tyrosine Kinases - genetics Review Rodents Topical application Tyrosine Ulcers Wound healing Wound Healing - genetics |
Title | Diabetic Foot Ulcers and Epidermal Growth Factor: Revisiting the Local Delivery Route for a Successful Outcome |
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