MOLECULAR GENETIC ABNORMALITIES
OF HEAD AND NECK CANCER
Koynova D* *Corresponding Author: Denitsa Koynova, Department of Medical Genetics, Institute of Obstetrics and GynecolŽogy, Medical University of Sofia, 2 Zdrave Str., 1431 Sofia, Bulgaria; Tel.: +359-2-952-03-57; Fax: +359-2-952-03-57; E-mail: dkkoiniva@hotmail.com page: 45
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CONCLUSIONS
Analysis of genetic alterations of HNSCC is of special interest because these genetic aberrations could serve as prognostic markers for survival assessment and treatment type. After evaluation of numerous studies, it has been concluded that EGFR, TGF-a, cyclin D1, p53, 3q and c-myc are reliable markers for HNSCC [35]. Unfortunately, information concerning the changes is insufficient, which warrants future investigations aimed at proving their role in tumor progression and patient treatment.
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