TY - JOUR T1 - MicroRNA Deregulation in Papillary Thyroid Cancer and its Relationship With BRAF V600E Mutation JF - In Vivo JO - In Vivo SP - 319 LP - 323 DO - 10.21873/invivo.12262 VL - 35 IS - 1 AU - PETR CELAKOVSKY AU - HELENA KOVARIKOVA AU - VIKTOR CHROBOK AU - JAN MEJZLIK AU - JAN LACO AU - HANA VOSMIKOVA AU - MARCELA CHMELAROVA AU - ALES RYSKA Y1 - 2021/01/01 UR - http://iv.iiarjournals.org/content/35/1/319.abstract N2 - Background: MicroRNAs (miRNAs) are non-coding regulatory molecules 18-25 nucleotides in length that act as post-transcriptional regulators of gene expression. MiRNAs affect various biological processes including carcinogenesis. Deregulation of miRNAa expression has been described in a variety of tumors including papillary thyroid carcinoma (PTC). The aim of the present study was to investigate the role of selected miRNAs in PTC and find associations between miRNA expression and the BRAF (V600E) mutation. Materials and Methods: The study group comprised a total of 62 patients with surgically treated PTC. The control group consisted of 30 patients with nodular goitre that were surgically treated in the same time period. The expression status of miR-146b, miR-181a, miR-187, miR-221 and miR-222 was determined using quantitative real-time PCR. BRAF mutation analysis was performed by PCR with reverse hybridization. Results: MiR-146b, miR-181a, miR-187, miR-221 and miR-222 were up-regulated in PTC compared to normal thyroid gland tissue of the same patient. MiR-146b, miR-187, miR-221 and miR-222 were also up-regulated in PTC compared to nodular goitre. The recurrent tumors were statistically significantly associated with up-regulation of miR-221. The mutation V600E of BRAF gene was significantly associated with up-regulation of miR-146b and with down-regulation of miR-187. Conclusion: Over-expression of selected miRNAs in PTC compared to normal thyroid gland tissue and nodular goitre was found. Moreover, miR-221 may serve as a prognostic marker as its over-expression was significantly associated with recurrent tumors. ER -