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Comparative genomic hybridization studies in tumours from a patient with multiple endocrine neoplasia type 1
S Kytölä1, M J Mäkinen, M Kähkönen
1Department of Clinical Genetics, Oulu University Hospital, Finland.
Objective:
To identify genetic changes, other than the MEN1 gene, that might be involved in the tumorigenesis and progression of multiple endocrine neoplasia type 1 (MEN1)-related tumours.
Methods:
We used comparative genomic hybridization (CGH) and loss of heterozygosity (LOH) to study tumours from various sites in a patient with MEN1.
Results:
Gain of genetic material was not found. Frequent losses of genetic material were found in chromosomes 1, 4, 5, 6, 9, 11 and 18. Besides the chromosome 11 where the MEN1 gene is located, the other regions are known to harbour important tumour suppressor genes.
Conclusions:
These results suggest the involvement of other cancer-related genes in the tumorigenesis and progression of MEN1 tumours that warrant further investigations.