Department of General and Pediatric Surgery, South Ural State Medical University, Chelyabinsk 454092, Russia.
Department of the Structure and Function of Chromosomes, Institute of Molecular and Cellular Biology, SB RAS, Novosibirsk 630090, Russia.
Int J Mol Sci. 2024 Jun 28;25(13):7090. doi: 10.3390/ijms25137090.
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 ( < 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 < < 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.
分子遗传事件是影响甲状腺乳头状癌(PTC)临床病程的众多因素之一。最近的研究表明,miRNA 的异常表达以及不同的甲状腺相关基因与 PTC 的侵袭性临床病程和不良治疗结果相关,这为它们在 PTC 患者治疗策略的个体化中应用开辟了新的途径。在本工作中,我们的目标是评估分子标志物在侵袭性甲状腺乳头状癌术前诊断中的适用性。对通过细针抽吸活检收集的 108 例具有不同临床表现的 PTC 患者的细胞学标本进行了分子遗传学特征(34 种不同标志物和 BRAF 突变的表达水平)研究。对具有临床侵袭性变异的 PTC 进行了调整后的多重比较(<0.0015)的统计学显著差异,获得了四个标志物:miRNA-146b、miRNA-221、纤维连接蛋白 1(FN1)和细胞周期蛋白依赖性激酶抑制剂 2A(CDKN2A)基因。miRNA-31、-375、-551b、-148b、-125b、mtDNA、CITED1、TPO、HMGA2、CLU、NIS、SERPINA1、TFF3 和 TMPRSS4 观察到弱的统计学相关性(0.0015 < < 0.05)。可以使用 miRNA-221、FN1 和 CDKN2A 基因术前预测甲状腺乳头状癌的复发风险。