Psoriasis: Striving for Potential Biomarkers.

IF 1.6 4区 医学 Q4 BIOCHEMICAL RESEARCH METHODS
Assay and drug development technologies Pub Date : 2023-08-01 Epub Date: 2023-09-05 DOI:10.1089/adt.2023.014
Deblina Dan, Nimisha Srivastava
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引用次数: 0

Abstract

Psoriasis is a chronic disease that is caused by multiple factors and is identified by itchiness, unpleasant, red, or white scaly patches on the skin, particularly on regularly chafed body regions such as the lateral areas of the limbs. Reports suggest that globally around 2%-3% of the population suffers from psoriasis. In this review, we have discussed the clinical classification of psoriasis and also the ideal characteristics of the biomarkers. An overview regarding the discovery of the biomarker and method for validating the study has been discussed. A growing body of research suggests a link to certain other systemic symptoms such as cardiovascular disorder, metabolic syndrome, and few other comorbidities such as hypertension and nonalcoholic fatty liver disease. Natural killer (NK) cells are lymphocyte cells that concentrate on the destruction of virally infected and malignant cells; these tend to produce a wide range of inflammatory cytokines, some of which are associated with the etiology of psoriasis. Detailed information on the molecular pathogenesis of psoriasis in which interleukin (IL)-17, IL-23, tumor necrosis factor-α (TNF-α), and CCL20 play a very significant role in the development of psoriasis. In this review, we have discussed an overview of the recent state of the biomarkers available for the diagnosis and treatment of psoriasis by emphasizing on the available biomarkers such as epigenomic, transcriptomic, glycomic, and metabolomic. The most recent advancements in molecular-targeted therapy utilizing biologics and oral systemic therapy (methotrexate, apremilast) enable to adequately treat the most serious psoriatic symptoms and also the studies have validated the efficacy of biologic therapy such as TNF-α antagonist (infliximab, adalimumab), IL-23 antagonist (guselkumab, risankizumab), and IL-17 antagonist (secukinumab, ixekizumab). Finally, an overview about the technological opportunities as well as various challenges has been discussed.

银屑病:寻找潜在的生物标志物。
银屑病是一种由多种因素引起的慢性疾病,表现为皮肤上的瘙痒、不适、红色或白色鳞状斑块,尤其是经常擦伤的身体部位,如四肢外侧区域。报告显示,全球约有2%-3%的人口患有银屑病。在这篇综述中,我们讨论了银屑病的临床分类以及生物标志物的理想特征。对生物标志物的发现和验证该研究的方法进行了综述。越来越多的研究表明,这与某些其他全身症状有关,如心血管疾病、代谢综合征,以及高血压和非酒精性脂肪肝等少数其他合并症。自然杀伤(NK)细胞是集中于破坏病毒感染和恶性细胞的淋巴细胞;这些往往会产生广泛的炎症细胞因子,其中一些与银屑病的病因有关。银屑病分子发病机制的详细信息,其中白细胞介素(IL)-17、IL-23、肿瘤坏死因子-α(TNF-α)和CCL20在银屑病的发展中起着非常重要的作用。在这篇综述中,我们通过强调可用的生物标志物,如表观基因组、转录组、糖组和代谢组,讨论了可用于银屑病诊断和治疗的生物标记物的最新状态。利用生物制剂和口服系统性治疗(甲氨蝶呤、阿培司特)的分子靶向治疗的最新进展能够充分治疗最严重的银屑病症状,研究也验证了生物治疗的疗效,如TNF-α拮抗剂(英夫利昔单抗、阿达木单抗)、IL-23拮抗剂,和IL-17拮抗剂(secukinumab、ixekizumab)。最后,对技术机遇和各种挑战进行了概述。
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来源期刊
Assay and drug development technologies
Assay and drug development technologies 医学-生化研究方法
CiteScore
3.60
自引率
0.00%
发文量
33
审稿时长
>12 weeks
期刊介绍: ASSAY and Drug Development Technologies provides access to novel techniques and robust tools that enable critical advances in early-stage screening. This research published in the Journal leads to important therapeutics and platforms for drug discovery and development. This reputable peer-reviewed journal features original papers application-oriented technology reviews, topical issues on novel and burgeoning areas of research, and reports in methodology and technology application. ASSAY and Drug Development Technologies coverage includes: -Assay design, target development, and high-throughput technologies- Hit to Lead optimization and medicinal chemistry through preclinical candidate selection- Lab automation, sample management, bioinformatics, data mining, virtual screening, and data analysis- Approaches to assays configured for gene families, inherited, and infectious diseases- Assays and strategies for adapting model organisms to drug discovery- The use of stem cells as models of disease- Translation of phenotypic outputs to target identification- Exploration and mechanistic studies of the technical basis for assay and screening artifacts
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