Genetic alterations in Hungarian patients with papillary thyroid cancer

The incidence of thyroid cancers is increasing worldwide. Some somatic oncogene mutations (BRAF, NRAS, HRAS, KRAS) as well as gene translocations (RET/PTC, PAX8/PPAR-gamma) have been associated with the development of thyroid cancer. In our study, we analyzed these genetic alterations in 394 th...

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Bibliographic Details
Main Authors: Tóbiás Bálint
Halászlaki Csaba
Balla Bernadett
Kósa János
Árvai Kristóf
Horváth Péter
Takács István
Nagy Zsolt
Horváth Evelin
Horányi János
Járay Balázs
Székely Eszter
Székely Tamás
Győri Gabriella
Putz Zsuzsanna
Dank Magdolna
Valkusz Zsuzsanna
Vasas Béla
Iványi Béla
Lakatos Péter
Format: Article
Published: Springer Netherlands 2016
Series:PATHOLOGY AND ONCOLOGY RESEARCH 22 No. 1
doi:10.1007/s12253-015-9969-9

mtmt:2927668
Online Access:http://publicatio.bibl.u-szeged.hu/13029
Description
Summary:The incidence of thyroid cancers is increasing worldwide. Some somatic oncogene mutations (BRAF, NRAS, HRAS, KRAS) as well as gene translocations (RET/PTC, PAX8/PPAR-gamma) have been associated with the development of thyroid cancer. In our study, we analyzed these genetic alterations in 394 thyroid tissue samples (197 papillary carcinomas and 197 healthy). The somatic mutations and translocations were detected by Light Cycler melting method and Real-Time Polymerase Chain Reaction techniques, respectively. In tumorous samples, 86 BRAF (44.2 %), 5 NRAS (3.1 %), 2 HRAS (1.0 %) and 1 KRAS (0.5 %) mutations were found, as well as 9 RET/PTC1 (4.6 %) and 1 RET/PTC3 (0.5 %) translocations. No genetic alteration was seen in the non tumorous control thyroid tissues. No correlation was detected between the genetic variants and the pathological subtypes of papillary cancer as well as the severity of the disease. Our results are only partly concordant with the data found in the literature.
Physical Description:27-33
ISSN:1219-4956