Literature DB >> 26543679

Chemokines as Therapeutic Targets to Improve Healing Efficiency of Chronic Wounds.

Latha Satish1.   

Abstract

Significance: Impaired wound healing leading to chronic wounds is an important clinical problem that needs immediate attention to develop new effective therapies. Members of the chemokine family seem to be attractive and amenable to stimulate the healing process in chronic wounds. Targeting specific chemokines and/or their receptors has the potential to modify chronic inflammation to acute inflammation, which will hasten the healing process. Recent Advances: Over the years, expression levels of various chemokines and their receptors have been identified as key players in the inflammatory phase of wound healing. In addition, they contribute to regulating other phases of wound healing making them key targets for novel therapies. Understanding the signaling pathways of these chemokines will provide valuable clues for modulating their function to enhance the wound healing process. Critical Issues: Inflammation, an important first-stage process in wound healing, is dysregulated in chronic wounds; emerging studies show that chemokines play a crucial role in regulating inflammation. The knowledge gained so far is still limited in understanding the enormous complexity of the chemokine network during inflammation not just in chronic wounds but also in acute (normal) wounds. A much better understanding of the individual chemokines will pave the way for better targets and therapies to improve the healing efficiency of chronic wounds. Future Directions: Effective understanding of the interaction of chemokines and their receptors during chronic wound healing would facilitate the design of novel therapeutic drugs. Development of chemokine-based drugs targeting specific inflammatory cells will be invaluable in the treatment of chronic wounds, in which inflammation plays a major role.

Entities:  

Year:  2015        PMID: 26543679      PMCID: PMC4620534          DOI: 10.1089/wound.2014.0602

Source DB:  PubMed          Journal:  Adv Wound Care (New Rochelle)        ISSN: 2162-1918            Impact factor:   4.730


  70 in total

1.  Transcriptional and post-transcriptional regulation of 72-kDa gelatinase/type IV collagenase by transforming growth factor-beta 1 in human fibroblasts. Comparisons with collagenase and tissue inhibitor of matrix metalloproteinase gene expression.

Authors:  C M Overall; J L Wrana; J Sodek
Journal:  J Biol Chem       Date:  1991-07-25       Impact factor: 5.157

Review 2.  Interactions between extracellular matrix and growth factors in wound healing.

Authors:  Gregory S Schultz; Annette Wysocki
Journal:  Wound Repair Regen       Date:  2009 Mar-Apr       Impact factor: 3.617

3.  Cultured pressure ulcer fibroblasts show replicative senescence with elevated production of plasmin, plasminogen activator inhibitor-1, and transforming growth factor-beta1.

Authors:  Jerry S Vande Berg; Michael A Rose; Patricia L Haywood-Reid; Ross Rudolph; Wyatt G Payne; Martin C Robson
Journal:  Wound Repair Regen       Date:  2005 Jan-Feb       Impact factor: 3.617

Review 4.  Update on tissue-engineered biological dressings.

Authors:  M Ehrenreich; Z Ruszczak
Journal:  Tissue Eng       Date:  2006-09

5.  Interleukin-1alpha and collagenase activity are elevated in chronic wounds.

Authors:  E J Barone; D R Yager; A L Pozez; O O Olutoye; M C Crossland; R F Diegelmann; I K Cohen
Journal:  Plast Reconstr Surg       Date:  1998-09       Impact factor: 4.730

6.  Efficacy and safety of becaplermin (recombinant human platelet-derived growth factor-BB) in patients with nonhealing, lower extremity diabetic ulcers: a combined analysis of four randomized studies.

Authors:  J M Smiell; T J Wieman; D L Steed; B H Perry; A R Sampson; B H Schwab
Journal:  Wound Repair Regen       Date:  1999 Sep-Oct       Impact factor: 3.617

7.  Improved diabetic wound healing through topical silencing of p53 is associated with augmented vasculogenic mediators.

Authors:  Phuong D Nguyen; John Paul Tutela; Vishal D Thanik; Denis Knobel; Robert J Allen; Christopher C Chang; Jamie P Levine; Stephen M Warren; Pierre B Saadeh
Journal:  Wound Repair Regen       Date:  2010-10-18       Impact factor: 3.617

8.  Stromal cell-derived factor-1 enhances wound healing through recruiting bone marrow-derived mesenchymal stem cells to the wound area and promoting neovascularization.

Authors:  Xiang Xu; Fangqiang Zhu; Meng Zhang; Dengfen Zeng; Donglin Luo; Guodong Liu; Wenhui Cui; Shali Wang; Wei Guo; Wei Xing; Huaping Liang; Lei Li; Xiaobing Fu; Jianxin Jiang; Hong Huang
Journal:  Cells Tissues Organs       Date:  2012-12-01       Impact factor: 2.481

Review 9.  Clinical application of growth factors and cytokines in wound healing.

Authors:  Stephan Barrientos; Harold Brem; Olivera Stojadinovic; Marjana Tomic-Canic
Journal:  Wound Repair Regen       Date:  2014 Sep-Oct       Impact factor: 3.617

10.  Deletion of a tumor necrosis superfamily gene in mice leads to impaired healing that mimics chronic wounds in humans.

Authors:  Melissa L Petreaca; Danh Do; Sandeep Dhall; Darcie McLelland; Avo Serafino; Julia Lyubovitsky; Neal Schiller; Manuela M Martins-Green
Journal:  Wound Repair Regen       Date:  2012 May-Jun       Impact factor: 3.617

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  2 in total

1.  Evaluation of wound healing effect of Mallotus philippensis (Lam.) Mull. Arg. by in silico multitargets directed for multiligand approach.

Authors:  Kaumudee S Bodas; Chandrakant D Bagul; Vaibhav M Shinde
Journal:  In Silico Pharmacol       Date:  2022-10-02

Review 2.  Topical gel-based biomaterials for the treatment of diabetic foot ulcers.

Authors:  James R Bardill; Melissa R Laughter; Michael Stager; Kenneth W Liechty; Melissa D Krebs; Carlos Zgheib
Journal:  Acta Biomater       Date:  2021-10-30       Impact factor: 8.947

  2 in total

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