Small molecules under development for psoriasis: on the road to the individualized therapies.
Calcium Release Activated Calcium Channels
/ antagonists & inhibitors
Cathepsins
/ antagonists & inhibitors
Dermatologic Agents
/ pharmacology
Drug Development
Gene Expression Regulation
/ drug effects
Humans
Nuclear Receptor Subfamily 1, Group F, Member 3
/ antagonists & inhibitors
Patient Satisfaction
Precision Medicine
/ methods
Psoriasis
/ drug therapy
Purine-Nucleoside Phosphorylase
/ antagonists & inhibitors
STAT3 Transcription Factor
/ antagonists & inhibitors
Individualized medicine
Pathogenesis
Psoriasis
Small molecules
Targets
Therapy
Journal
Archives of dermatological research
ISSN: 1432-069X
Titre abrégé: Arch Dermatol Res
Pays: Germany
ID NLM: 8000462
Informations de publication
Date de publication:
Nov 2020
Nov 2020
Historique:
received:
25
11
2019
accepted:
26
02
2020
pubmed:
17
3
2020
medline:
27
5
2021
entrez:
16
3
2020
Statut:
ppublish
Résumé
Psoriasis is an incurable cutaneous illness characterized by the presence of well-delimited reddish plaques and silvery-white dry scales. So far, there is a limited understanding of its pathogenesis, though recent discoveries on the immunological, genetic and molecular aspects of this disease have significantly contributed to the identification of new targets and the development of novel drugs. Despite these advances, many patients are still dissatisfied, so to improve patient satisfaction, reliability, and clinical outcomes, the individualization of the treatments for this disease becomes a necessity. This review summarizes recent findings related to psoriasis pathogenesis and describes new small molecules and targets recently identified as promising for treatments. Additionally, the current status, challenges and the future directions for achieving individualized therapy for this disease and the need for more collaborative studies are discussed. The individualization of treatments for psoriasis, rather than a goal, is analyzed as a process where a dynamic integration between the needs and characteristics of the patients, the pharmacological progress, and the clinical decisions takes place.
Identifiants
pubmed: 32172339
doi: 10.1007/s00403-020-02056-3
pii: 10.1007/s00403-020-02056-3
doi:
Substances chimiques
Calcium Release Activated Calcium Channels
0
Dermatologic Agents
0
Nuclear Receptor Subfamily 1, Group F, Member 3
0
RORC protein, human
0
STAT3 Transcription Factor
0
STAT3 protein, human
0
Purine-Nucleoside Phosphorylase
EC 2.4.2.1
Cathepsins
EC 3.4.-
cathepsin S
EC 3.4.22.27
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM