Brought to you by Portland Press Ltd.
Published on behalf of the International Federation for Cell Biology
Cancer Cell death Cell cycle Cytoskeleton Exo/endocytosis Differentiation Division Organelles Signalling Stem cells Trafficking
Cell Biology International (2007) 31, 215–219 (Printed in Great Britain)
Evaluation of aneuploidy frequency for chromosomes 6 and 17 in eyelid tumours using the FISH technique
Ahmet Özkağnicia, Hasan Acarb*, Nazmi Zengina and Süleyman Okudana
aDepartment of Ophthalmology, Selçuk University, Meram Medical Faculty, Konya 42080, Turkey
bDepartment of Medical Genetics, Selçuk University, Meram Medical Faculty, Konya 42080, Turkey


Abstract

Although basal cell carcinoma (BCC) and squamous cell carcinoma (SCC) are very common skin tumours, the incidence of chromosome aneuploidy with regard to the eyelid has not been investigated. We aimed to find the frequency of chromosome 6 and 17 aneuploidies in eyelid tumours' interphase nuclei with fluorescence in situ hybridization (I-FISH) with chromosome specific DNA probes. I-FISH with chromosome 6 and 17 centromere specific DNA probes was used in the eyelids of 10 patients with BCC or SCC and the peripheral blood cells of 10 healthy donors as controls. The frequency of chromosome 6 and 17 aneuploidies was significantly higher in 7 out of 10 patients and 5 out of 10 patients, respectively, than in controls, indicating a higher frequency of aneuploidy in BCC than in SCC of the eyelid. Distribution of hybridization signals for chromosome 6 and 17 was wide ranging, indicating heterogeneity of cell populations with aneuploidy between patients. These findings indicate that acquisition of chromosome aneuploidies in eyelid tumours may have an important pathogenic role in both BCC and SCC of the eyelid area.


Key words: Basal cell carcinoma, Squamous cell carcinoma, Choromosome 6, Choromosome 17, FISH, Interphase nuclei, Eyelid.

*Corresponding author. Tel.: +90 332 223 6662; fax: +90 332 223 6181.


Received 10 February 2006/5 September 2006; accepted 11 October 2006

doi:10.1016/j.cellbi.2006.10.003


ISSN Print: 1065-6995
ISSN Electronic: 1095-8355
Published by Portland Press Limited on behalf of the International Federation for Cell Biology (IFCB)