3.9 Article

INCIDENCE AND CLINICAL RELEVANCE OF T(11;19) TRANSLOCATION IN SALIVARY GLAND MUCOEPIDERMOID CARCINOMA

Journal

GENETIKA-BELGRADE
Volume 46, Issue 2, Pages 601-610

Publisher

SERBIAN GENETICS SOC
DOI: 10.2298/GENSR1402601D

Keywords

Salivary gland; Mucoepidermoid carcinoma; Chromosomal translocation (11,19); MECT1-MAML2; RT-PCR diagnostic

Funding

  1. Ministry of Education, Science and Technological Development of Serbia [175075]
  2. Institute of Haematopathology Hamburg, Hamburg, Germany

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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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