Prediction of the Aggressive Clinical Course of Papillary Thyroid Carcinoma Based on Fine Needle Aspiration Biopsy Molecular Testing.
Humans
Biopsy, Fine-Needle
Thyroid Cancer, Papillary
/ genetics
Female
Thyroid Neoplasms
/ genetics
Male
Biomarkers, Tumor
/ genetics
MicroRNAs
/ genetics
Middle Aged
Adult
Proto-Oncogene Proteins B-raf
/ genetics
Mutation
Aged
Fibronectins
/ genetics
Cyclin-Dependent Kinase Inhibitor p16
/ genetics
Gene Expression Regulation, Neoplastic
Prognosis
CDKN2A
FN1
aggressive variants
miRNA-146b
miRNA-221
papillary thyroid carcinoma
recurrence risk
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:
28 Jun 2024
28 Jun 2024
Historique:
received:
31
05
2024
revised:
19
06
2024
accepted:
24
06
2024
medline:
13
7
2024
pubmed:
13
7
2024
entrez:
13
7
2024
Statut:
epublish
Résumé
Molecular genetic events are among the numerous factors affecting the clinical course of papillary thyroid carcinoma (PTC). Recent studies have demonstrated that aberrant expression of miRNA, as well as different thyroid-related genes, correlate with the aggressive clinical course of PTC and unfavorable treatment outcomes, which opens up new avenues for using them in the personalization of the treatment strategy for patients with PTC. In the present work, our goal was to assess the applicability of molecular markers in the preoperative diagnosis of aggressive variants of papillary thyroid cancer. The molecular genetic profile (expression levels of 34 different markers and BRAF mutations) was studied for 108 cytology specimens collected by fine-needle aspiration biopsy in patients with PTC having different clinical manifestations. Statistically significant differences with adjustment for multiple comparisons (
Identifiants
pubmed: 39000197
pii: ijms25137090
doi: 10.3390/ijms25137090
pii:
doi:
Substances chimiques
Biomarkers, Tumor
0
MicroRNAs
0
Proto-Oncogene Proteins B-raf
EC 2.7.11.1
Fibronectins
0
FN1 protein, human
0
BRAF protein, human
EC 2.7.11.1
Cyclin-Dependent Kinase Inhibitor p16
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Subventions
Organisme : Russian Science Foundation
ID : 20-14-00074-P