Literature DB >> 34480483

Novel targets and therapies for keloid.

P P Naik1.   

Abstract

Keloids are the result of aberrant tissue scarring typically occurring in injured skin, and are caused by the overgrowth of granulation tissue or collagen type III during the healing process. There is a genetic component, thus a predisposition can be genetically transmitted. Keloids are difficult to treat because of their postexcisional recurrence, and they have an impact on patient quality of life due to psychological distress caused by cosmetic concerns and functional disability. Treatment ranges from classic corticosteroid therapy to multimodal approaches such as injections, cryotherapy, laser, radiation, radiofrequency ablation and extracorporeal shockwave therapy. Recent discoveries into the pathogenesis of keloid have enabled clinicians to expand the therapeutic options for treatment. The aim of this paper was to review the literature, clarify the general concept of keloid development, and assess emerging treatment options such as stem cell therapy, mitomycin C, bleomycin, interferon, botulinum toxin type A, calcium channel blockers, angiotensin-converting enzyme inhibitors and fat grafting, and the evolutionary advancement towards epigenetic modifications and gene therapy.
© 2021 British Association of Dermatologists.

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Mesh:

Year:  2021        PMID: 34480483     DOI: 10.1111/ced.14920

Source DB:  PubMed          Journal:  Clin Exp Dermatol        ISSN: 0307-6938            Impact factor:   3.470


  3 in total

1.  Detection and analysis of long noncoding RNA expression profiles related to epithelial-mesenchymal transition in keloids.

Authors:  Zhixiong Chen; Xi Chu; Jinghong Xu
Journal:  Biomed Eng Online       Date:  2022-01-11       Impact factor: 2.819

2.  Comprehensive Analysis of Chromatin Accessibility and Transcriptional Landscape Identified BRCA1 Repression as a Potential Pathological Factor for Keloid.

Authors:  Kuixia Xie; Jingrun Yang; Qianqian Yao; Yang Xu; Yonglin Peng; Xinhua Liu
Journal:  Polymers (Basel)       Date:  2022-08-19       Impact factor: 4.967

3.  Silencing circular RNAPTPN12 promoted the growth of keloid fibroblasts by activating Wnt signaling pathway via targeting microRNA-21-5p.

Authors:  Fei Liu; Tao Li; Xiaoan Zhan
Journal:  Bioengineered       Date:  2022-02       Impact factor: 3.269

  3 in total

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