
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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Abstract
Head and neck cancers are a heterogeneous group of diseases. The development of these tumors is a consequence of genetic mutations which influene the activity of oncogenes such as CCND1, c-myc, erbB and ras, as well as the function of tumor suppressor genes: p53, Rb, p16, p21, and p27. The investigation of these genetic changes has been done through the application of a variety of genetic methods. The knowledge of the genetic changes which occur in the mucosa of the head and neck region through the different steps of tumorogenesis is very important for both patient and diagnosis and treatment.
Key words: Head and neck tumors; Head and neck squamous cell carcinoma (HNSCC); Oncogenes; Tumor suppressor genes.
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