Research output: Contribution to journal › Article › peer-review
Prediction of the Aggressive Clinical Course of Papillary Thyroid Carcinoma Based on Fine Needle Aspiration Biopsy Molecular Testing. / Lukyanov, Sergei A.; Titov, Sergei E.; Kozorezova, Evgeniya S. et al.
In: International Journal of Molecular Sciences, Vol. 25, No. 13, 7090, 07.2024.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Prediction of the Aggressive Clinical Course of Papillary Thyroid Carcinoma Based on Fine Needle Aspiration Biopsy Molecular Testing
AU - Lukyanov, Sergei A.
AU - Titov, Sergei E.
AU - Kozorezova, Evgeniya S.
AU - Demenkov, Pavel S.
AU - Veryaskina, Yulia A.
AU - Korotovskii, Denis V.
AU - Ilyina, Tatyana E.
AU - Vorobyev, Sergey L.
AU - Zhivotov, Vladimir A.
AU - Bondarev, Nikita S.
AU - Sleptsov, Ilya V.
AU - Sergiyko, Sergei V.
N1 - This research was funded by the Russian Science Foundation, grant number 20-14-00074-P.
PY - 2024/7
Y1 - 2024/7
N2 - 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 (p < 0.0015) for clinically aggressive variants of PTC were obtained for four markers: miRNA-146b, miRNA-221, fibronectin 1 (FN1), and cyclin-dependent kinase inhibitor 2A (CDKN2A) genes. A weak statistical correlation (0.0015 < p < 0.05) was observed for miRNA-31, -375, -551b, -148b, -125b, mtDNA, CITED1, TPO, HMGA2, CLU, NIS, SERPINA1, TFF3, and TMPRSS4. The recurrence risk of papillary thyroid carcinoma can be preoperatively predicted using miRNA-221, FN1, and CDKN2A genes.
AB - 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 (p < 0.0015) for clinically aggressive variants of PTC were obtained for four markers: miRNA-146b, miRNA-221, fibronectin 1 (FN1), and cyclin-dependent kinase inhibitor 2A (CDKN2A) genes. A weak statistical correlation (0.0015 < p < 0.05) was observed for miRNA-31, -375, -551b, -148b, -125b, mtDNA, CITED1, TPO, HMGA2, CLU, NIS, SERPINA1, TFF3, and TMPRSS4. The recurrence risk of papillary thyroid carcinoma can be preoperatively predicted using miRNA-221, FN1, and CDKN2A genes.
KW - CDKN2A
KW - FN1
KW - aggressive variants
KW - miRNA-146b
KW - miRNA-221
KW - papillary thyroid carcinoma
KW - recurrence risk
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85198452625&origin=inward&txGid=85759b37960caf5bb539fbc04d40600a
UR - https://www.mendeley.com/catalogue/f7ed0a71-32fb-3b07-958e-549430f764aa/
U2 - 10.3390/ijms25137090
DO - 10.3390/ijms25137090
M3 - Article
C2 - 39000197
VL - 25
JO - International Journal of Molecular Sciences
JF - International Journal of Molecular Sciences
SN - 1661-6596
IS - 13
M1 - 7090
ER -
ID: 60850658