Transient receptor potential cation channel subfamily V member 1 (TRPV1) targeted PET imaging.
PET/CT
TRPV1
cancer
pain
transient receptor potential cation channel subfamily V member 1
Journal
Japanese journal of clinical oncology
ISSN: 1465-3621
Titre abrégé: Jpn J Clin Oncol
Pays: England
ID NLM: 0313225
Informations de publication
Date de publication:
20 Jan 2024
20 Jan 2024
Historique:
received:
19
10
2023
accepted:
27
12
2023
medline:
22
1
2024
pubmed:
22
1
2024
entrez:
22
1
2024
Statut:
aheadofprint
Résumé
Transient receptor potential cation channel subfamily V member 1 (TRPV1) was identified using capsaicin, a pungent compound that is present in red pepper. The activation of TRPV1 induces an influx of calcium ions into cells and causes excitation of sensory neurons, associating with thermal sensing, sweating and pain. TRPV1 is also identified in various types of cancer cells. The expression of TRPV1 in cancer cells depends on the type of cancer and the stage of the disease. Therefore, TRPV1 has been considered a potential target of medicinal chemistry for drug development, and blocking its activation may lead to cancer therapy and pain relief. However, the details of the pathophysiological function of TRPV1 in vivo are still unclear. To explore practical use of TRPV1, we focused on positron emission tomography imaging and developed a 11C-radiolabeled tracer to visualize TRPV1.
Identifiants
pubmed: 38251773
pii: 7584463
doi: 10.1093/jjco/hyad194
pii:
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Individual Knowledge Research in FY 2012 Strategic Programs for R&D
Organisme : Translational Research Program
ID : A120
Organisme : Japan Agency for Medical Research and Development
Organisme : Ministry of Health, Labour and Welfare Grants and Japan Agency for Medical Research and Development
ID : 21K07668
Informations de copyright
© The Author(s) 2024. Published by Oxford University Press. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.