Navigating the landscape of psoriasis therapy: novel targeted pathways and emerging trends

被引:3
作者
Innani, Srinath [1 ]
Tomar, Yashika [1 ]
Rana, Vikas [2 ]
Singhvi, Gautam [1 ,3 ]
机构
[1] Birla Inst Technol & Sci BITS, Dept Pharm, Ind Res Lab, Pilani, Rajasthan, India
[2] Punjabi Univ, Dept Pharmaceut Sci & Drug Res, Patiala, Punjab, India
[3] Birla Inst Technol & Sci BITS Pilani, Dept Pharm, Pilani Campus, Pilani, Rajasthan, India
关键词
Adenosine A3 receptor; molecular targets; aryl hydrogen receptor pathway (AhR); psoriasis; sphingosine 1 phosphate (S1P); ARYL-HYDROCARBON RECEPTOR; GENE-RELATED PEPTIDE; A(3) ADENOSINE RECEPTOR; SPHINGOSINE-1-PHOSPHATE; DELIVERY; INFLAMMATION; ACTIVATION; TAPINAROF; PROTEINS; RELEASE;
D O I
10.1080/14728222.2023.2288273
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
IntroductionPsoriasis is a chronic, inflammatory, non-communicable skin disorder that affects a patient's social and emotional well-being. It is characterized by hyperproliferation of keratinocytes, irregular shedding of skin cells, and abnormal invasion of inflammatory mediators. The treatment strategy is designed based on the severity of the disease condition starting from topical, phototherapy, systemic, and biologics. In recent years, extensive research into the underlying mechanisms of psoriasis has led to significant advancement in treatment options from small molecules to biologics.Area coveredThis review focuses on intracellular and molecular mechanisms such as AhR, A3AR, RIP1, CGRP, and S1P that serve as novel pharmacological targets for psoriasis. Moreover, new molecules are approved or are under clinical investigation to interfere with these target mechanisms.Expert opinionA detailed understanding of signaling pathways provides potential targets and molecular mechanisms for the inflammatory cascade in psoriasis. This has led to the development of small molecules targeting specific pathways. Further, the combination of nanotechnology can assist in dose reduction leading to reduced adverse effects in the management of psoriasis.
引用
收藏
页码:1247 / 1256
页数:10
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