光生物调节疗法对皮肤伤口愈合中基因表达的调节:体内研究系统综述。

IF 2.5 4区 医学 Q2 DERMATOLOGY Photodermatology, photoimmunology & photomedicine Pub Date : 2024-07-01 DOI:10.1111/phpp.12990
Emily Ferreira Salles Pilar, Fernanda Thomé Brochado, Tuany Rafaeli Schmidt, Amanda Costa Leite, Alexia Antunes Deluca, Belkiss Câmara Mármora, Marina Siebert, Vivian Petersen Wagner, Manoela Domingues Martins
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引用次数: 0

摘要

背景:伤口愈合是一个多步骤的过程,涉及多种细胞类型、细胞因子、生长因子和细胞外基质(ECM)成分的协调反应,从而导致组织完整性的生理性恢复。光生物调控疗法(PBMT)作为一种改善愈合过程的方法已受到重视,但在分子水平上,人们对光生物调控疗法的影响还不完全了解:在 Medline Ovid (Wolters Kluwer)、PubMed (National Library of Medicine)、Web of Science (Thomson Reuters)、Scopus (Elsevier)、Embase 和 LILACS 数据库中进行电子检索。搜索策略以低水平光疗法、基因表达和伤口愈合及其同义词为关键词。数据库的查询时间为 2023 年 12 月,没有使用出版年份限制:本综述共纳入 11 项研究,评估了 186 个基因的表达。PBMT 改变了所研究的几个靶基因的表达,如下调与细胞外基质蛋白酶(MMP2 和 MMP9)和促炎细胞因子(IL10 和 IL6)相关的基因,上调 DNMT3A 和 BFGF:本综述表明,PBMT 能够调节伤口愈合过程中的基因表达。大多数证据显示,PBMT 在调节与炎性细胞因子相关的基因方面具有积极影响,可改善皮肤伤口愈合。然而,PBMT 对参与其他机制的基因的影响仍有待进一步了解。
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Modulation of gene expression in skin wound healing by photobiomodulation therapy: A systematic review in vivo studies.

Background: Wound healing is a multistep process involving coordinated responses of a variety of cell types, cytokines, growth factors, and extracellular matrix (ECM) components leading to the physiological restoration of tissue integrity. Photobiomodulation therapy (PBMT) has been highlighted as an approach to improve the healing process, nonetheless at the molecular level, the effects of PBMT are not entirely understood.

Aim: To systematically review publications that investigated gene expression after PBMT during in vivo skin repair.

Methods: An electronic search was undertaken in Medline Ovid (Wolters Kluwer), PubMed (National Library of Medicine), Web of Science (Thomson Reuters), Scopus (Elsevier), Embase, and LILACS databases. The search strategy was conducted from the terms: low-level light therapy, gene expression, and wound healing and their synonyms. The databases were consulted in December 2023 and no publication year limit was used.

Results: Eleven studies were included in this review and the expression of 186 genes was evaluated. PBMT modified the expression of several targets genes studied, such as down-regulation of genes related to extracellular matrix proteases (MMP2 and MMP9) and pro-inflammatory cytokines (IL10 and IL6) and up-regulation of DNMT3A and BFGF.

Conclusion: This review demonstrates that PBMT is capable of regulating gene expression during wound healing. Most evidence showed a positive impact of PBMT in regulating genes linked to inflammatory cytokines improving skin wound healing. Yet, the effects of PBMT in genes involved in other mechanisms still need to be better understood.

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来源期刊
CiteScore
4.40
自引率
7.70%
发文量
85
审稿时长
6-12 weeks
期刊介绍: The journal is a forum for new information about the direct and distant effects of electromagnetic radiation (ultraviolet, visible and infrared) mediated through skin. The divisions of the editorial board reflect areas of specific interest: aging, carcinogenesis, immunology, instrumentation and optics, lasers, photodynamic therapy, photosensitivity, pigmentation and therapy. Photodermatology, Photoimmunology & Photomedicine includes original articles, reviews, communications and editorials. Original articles may include the investigation of experimental or pathological processes in humans or animals in vivo or the investigation of radiation effects in cells or tissues in vitro. Methodology need have no limitation; rather, it should be appropriate to the question addressed.
期刊最新文献
Subjective and objective assessment of color match of universal tinted sunscreens in Fitzpatrick skin phototypes I-VI. Immunofluorescence findings in a reactivating lichenoid photoallergic chronic dermatitis (actinic reticuloid). Sunscreens prescribed to patients with skin of color and/or with melasma: A survey of 221 dermatologists and dermatology residents in Spain. Phototherapy for the treatment of cutaneous graft-versus-host disease: A systematic review. KGF-2 ameliorates UVB-triggered skin photodamage in mice by attenuating DNA damage and inflammatory response and mitochondrial dysfunction.
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