Suppr超能文献

瘢痕疙瘩疾病中的分子信号传导及基于天然化合物的当前治疗方法。

Molecular signalings in keloid disease and current therapeutic approaches from natural based compounds.

作者信息

Unahabhokha Thitita, Sucontphunt Apirada, Nimmannit Ubonthip, Chanvorachote Pithi, Yongsanguanchai Nuttida, Pongrakhananon Varisa

机构信息

Department of Pharmaceutical and Industrial, Pharmaceutical Technology , Chulalongkorn University, Bangkok , Thailand .

出版信息

Pharm Biol. 2015 Mar;53(3):457-63. doi: 10.3109/13880209.2014.918157. Epub 2014 Oct 21.

Abstract

CONTEXT

Keloid is an excessive dermal scar occurring in response to skin injuries. Several therapeutic strategies have been proposed to ease the aggressiveness of keloid scarring. Even though the principle mechanism underlying the disease propagation still remains unidentified, several signaling pathways were highly focused as plausible pathways involving keloid formation, including transforming growth factor-beta 1 (TGF-β1), mitogen-activated protein kinase (MAPK), insulin-like growth factor-I (IGF-I), and integrin pathways. Natural compounds containing multiple bioeffective properties such as quercetin, asiaticoside, Astragalus membranaceus Bunge. (Leguminosae), and Salvia miltiorrhiza Bunge. (Lamiaceae) extracts, curcuminoids, oxymatrine, madecassoside, and Aneilema keisak Hassk. (Commelinaceae) are claimed as candidates for therapeutic treatment against keloid disorder.

OBJECTIVE

This review investigates current mechanisms regarding keloid formation and provides scientific evidence supporting the therapeutic potential of natural compounds.

METHODS

This review obtained and analyzed a number of literature data items from various databases including Pubmed, ScienceDirect, and Elton B. Stephens Company (EBSCO).

RESULT

Several phytochemical compounds are able to suppress keloid scar development through manipulating various components in the complex signaling cascades.

CONCLUSION

The present review may be helpful to future studies that further examine the molecular mechanism of keloid etiology as well as investigate the anti-keloid property in natural compounds.

摘要

背景

瘢痕疙瘩是一种因皮肤损伤而产生的过度真皮瘢痕。人们已经提出了几种治疗策略来减轻瘢痕疙瘩瘢痕形成的侵袭性。尽管该疾病传播的主要机制仍未明确,但一些信号通路作为瘢痕疙瘩形成的可能通路受到了高度关注,包括转化生长因子-β1(TGF-β1)、丝裂原活化蛋白激酶(MAPK)、胰岛素样生长因子-I(IGF-I)和整合素通路。含有多种生物活性特性的天然化合物,如槲皮素、积雪草苷、黄芪(豆科)提取物、丹参(唇形科)提取物、姜黄素、氧化苦参碱、羟基积雪草苷和鸭跖草,被认为是治疗瘢痕疙瘩疾病的候选药物。

目的

本综述研究了目前关于瘢痕疙瘩形成的机制,并提供了支持天然化合物治疗潜力的科学证据。

方法

本综述从包括PubMed、ScienceDirect和EBSCO在内的多个数据库中获取并分析了大量文献数据。

结果

几种植物化学化合物能够通过操纵复杂信号级联中的各种成分来抑制瘢痕疙瘩瘢痕的发展。

结论

本综述可能有助于未来进一步研究瘢痕疙瘩病因分子机制以及天然化合物抗瘢痕疙瘩特性的研究。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验