Melatonin Receptor Expression in Primary Uveal Melanoma.
Humans
Uveal Neoplasms
/ metabolism
Melanoma
/ metabolism
Male
Female
Middle Aged
Receptor, Melatonin, MT1
/ metabolism
Aged
Nuclear Receptor Subfamily 1, Group F, Member 1
/ metabolism
Ubiquitin Thiolesterase
/ metabolism
Receptor, Melatonin, MT2
/ metabolism
Gene Expression Regulation, Neoplastic
Tumor Suppressor Proteins
/ genetics
Prognosis
Adult
Aged, 80 and over
Mutation
Melatonin
/ metabolism
Kaplan-Meier Estimate
adjuvant treatment
immunohistochemistry
melatonin
metastasis
prognostic factors
receptor expression
uveal melanoma
Journal
International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791
Informations de publication
Date de publication:
09 Aug 2024
09 Aug 2024
Historique:
received:
04
07
2024
revised:
05
08
2024
accepted:
06
08
2024
medline:
31
8
2024
pubmed:
31
8
2024
entrez:
29
8
2024
Statut:
epublish
Résumé
Melatonin, noted for its anti-cancer properties in various malignancies, including cutaneous melanoma, shows promise in Uveal melanoma (UM) treatment. This study aimed to evaluate melatonin receptor expression in primary UM and its association with UM-related mortality and prognostic factors. Immunohistochemical analysis of 47 primary UM tissues showed low expression of melatonin receptor 1A (MTNR1A) and melatonin receptor 1B (MTNR1B), with MTNR1A significantly higher in patients who succumbed to UM. Analysis of TCGA data from 80 UM patients revealed RNA expression for MTNR1A, retinoic acid-related orphan receptor alpha (RORα), and N-ribosyldihydronicotinamide:quinone oxidoreductase (NQO2), but not MTNR1B or G protein-coupled receptor 50 (GPR50). Higher MTNR1A RNA levels were observed in patients with a BRCA1 Associated Protein 1 (BAP1) mutation, and higher NQO2 RNA levels were noted in patients with the epithelioid tumor cell type. However, Kaplan-Meier analysis did not show distinct survival probabilities based on receptor expression. This study concludes that UM clinical samples express melatonin receptors, suggesting a potential mechanism for melatonin's anti-cancer effects. Despite finding higher MTNR1A expression in patients who died of UM, no survival differences were observed.
Identifiants
pubmed: 39201396
pii: ijms25168711
doi: 10.3390/ijms25168711
pii:
doi:
Substances chimiques
Receptor, Melatonin, MT1
0
Nuclear Receptor Subfamily 1, Group F, Member 1
0
Ubiquitin Thiolesterase
EC 3.4.19.12
RORA protein, human
0
BAP1 protein, human
0
Receptor, Melatonin, MT2
0
MTNR1B protein, human
0
MTNR1A protein, human
0
Tumor Suppressor Proteins
0
Melatonin
JL5DK93RCL
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Karolinska Institutet
ID : 2022-01671
Organisme : Region Stockholm
ID : RS-2019-1138
Organisme : The Swedish Cancer Society
ID : 20 0798 Fk
Organisme : The Crown Princess Margareta Foundation for the Visually Impaired
ID : 2022-017
Organisme : The Swedish Eye Foundation
ID : 2022-05-09