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XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

XXII. BIOCHEMICKÝ ZJAZD - Jesseniova lekárska fakulta

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Posters<br />

26.<br />

THE ASSOCIATION BETWEEN EGF 61 G/A POLYMORPHISM AND<br />

COLORECTAL CANCER DEVELOPMENT<br />

Silvia Mahmood, Tatiana Matáková, Lucia Letková, Monika Kmeťová Sivoňová,<br />

Jozef Hatok and Dušan Dobrota<br />

Department of Medical Biochemistry, Jessenius Faculty of Medicine,<br />

Comenius University, Martin, Slovakia<br />

The epidermal growth factor (EGF) gene has been demonstrated to participate in the<br />

pathogenesis or maintenance of several human cancers of epithelial origin. The purpose<br />

of the present case-control study was to investigate the association of the single-nucleotide<br />

polymorphism of EGF + 61 G/A with the susceptibility to colorectal cancer (CRC)<br />

in a population in the north of Slovakia. We have analyzed the genotype distribution of<br />

this polymorphism in 120 patients (65 [54,2%] men and 55 [45,8%] women, mean age<br />

64,2 years) and 110 healthy subjects, using the PCR-RFLP technique. Differences in allele<br />

and genotype frequencies were evaluated by the Chi-square (c 2 ) and Fisher exact tests.<br />

Our data suggests that EGF +61 G/A polymorphism may be used as a genetic susceptibility<br />

marker for CRC. With the aim to inhibit cancer growth and to reduce the risk of<br />

metastasis we adapt an avascular tumour growth model to simulate the effects of drug<br />

application on multicell spheroid (MCS) [1, 2].<br />

Acknowledgement: This work was supported by project “Creating a new diagnostic algorithm<br />

for selected cancer diseases” co-financed from EC sources and European Regional<br />

Development Fund.<br />

References<br />

(1) Mahmood, M., Mahmood, S. Dobrota, D. (2010): A numerical algorithm for avascular<br />

tumor growth model. Math. Comp. Sim., Vol. 80 (6): 1269-1277.<br />

(2) Ward JP, King JR (2003): Mathematical modelling of drug transport in tumour MCS<br />

and monolayer cultures. Math. Biosci., 181(2):177-207.<br />

<strong>XXII</strong>. Biochemistry Congress, Martin<br />

143

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