Incidence and clinical relevance of T(11;19) translocation in salivary gland mucoepidermoid carcinoma
Author(s) -
Ivana Ilic-Dimitrijevic,
Thomas Löning,
Marcus Falk,
Vitomir S. Konstantinović,
Miroslav Vukadinović,
Zvezdana Tepavčević,
Saša Tabaković,
Nataša Pejčić,
Biljana Miličić,
Jelena Milašin
Publication year - 2014
Publication title -
genetika
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.24
H-Index - 15
eISSN - 1820-6069
pISSN - 0534-0012
DOI - 10.2298/gensr1402601d
Subject(s) - mucoepidermoid carcinoma , chromosomal translocation , incidence (geometry) , clinical significance , oncogene , salivary gland , stage (stratigraphy) , carcinoma , histology , medicine , oncology , biology , pathology , gastroenterology , cancer research , cancer , cell cycle , genetics , gene , paleontology , physics , optics
Mucoepidermoid carcinoma (MEC) harbors a recurring t(11;19) translocation with an associated novel fusion oncogene-MECT1-MAML2. The CRTC1-MAML2oncogene disrupts normal cell-cycle and differentiation, contributing to tumor development. The objectives of this study were to establish the incidence of CRTC1-MAML2 fusion in Serbian patients and estimate its relevance as a genetic marker of MEC behavior. In this retrospective study, 20 cases of MEC of salivary glands were tested for the presence of CRTC1-MAML2 fusion using reverse transcriptase-polymerase chain reaction. Clinicopathological parameters and survival data were examined in relation to fusion status. The CRTC1-MAML2 fusion was detected in 40% of MECs and its presence was associated exclusively with low-intermediate grade tumor histology (P = 0.02) and favorable clinical outcome, with 100 % overall survival rate (P=0.046). The study has shown that the presence of the CRTC1-MAML2 fusion can serve as an additional diagnostic and prognostic marker for mucoepidermoid carcinomas
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