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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 />

117.<br />

ELLIPTICINE CYTOTOXICITY TO HUMan THYrOID caNCEr CELL LINES<br />

Jitka Poljaková 1 , Tomáš Eckschlager 2 , Eva Frei 1 and Marie Stiborová 1<br />

1<br />

Department of Biochemistry, Faculty of Science, Charles University in Prague,<br />

2<br />

Department of Pediatric Hematology and Oncology,<br />

2 nd Medical School, Charles University in Prague<br />

Ellipticines are plant alkaloids with an antineoplastic activity. The mode of action is based<br />

mainly on DNA intercalation, inhibition of topoisomerase II and formation of covalent<br />

DNA adducts mediated by cytochromes P450 (CYP) and peroxidases. Such ellipticine-<br />

DNA-adducts are formed in vitro, in human breast adenocarcinoma MCF-7, leukemia<br />

HL-60, CCRF-CEM, neuroblastoma IMR-32, UKF-NB-3, UKF-NB-4 cell lines and in vivo in<br />

rats exposed to ellipticine. Here, the cytotoxicity of ellipticine to human thyroid cancer<br />

cell lines BHT-101, B-CPAP and 8505-C was investigated. Furthermore, the effect of hypoxic<br />

conditions on the ellipticine toxicity to these cells was also examined. The toxicity<br />

of ellipticine to thyroid cancer cells cultivated under the standard conditions was higher<br />

than that to the cell lines grown under hypoxia (1% oxygen). Another target of this work<br />

was to evaluate the effect of ellipticine on expression of enzymes activating ellipticine,<br />

namely on CYP1A1, 1B1, 3A4, cytochrome b 5<br />

and peroxidases COX-1 and TPO.<br />

Acknowledgement: Supported by GACR (P301/10/0356) and Czech Ministry of Education<br />

(MSM0021620813).<br />

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

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