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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 />

35.<br />

GENEraTION aND CHaraCTErIZaTION MONOCLONal aNTIBODIES<br />

agaINST ENDOSIaLIN, THE POTENTIal marKEr of TUMOr<br />

aNGIOGENESIS<br />

Soňa Kontseková, Anna Repič, Monika Baráthová,<br />

Katarína Polčicová and Jaromír Pastorek<br />

Institute of Virology, SAS, Dúbravská cesta 9, 84505 Bratislava<br />

Endosialin, also known as TEM1, or CD248, was first discovered with the monoclonal<br />

antibody (mAb) Fb5 as an experimental approach to identify new targets for anti-cancer<br />

strategies. It was described as a transmembrane glycoprotein selectively expressed on<br />

tumor endothelium, but its expression is barely detectable in normal human tissue.<br />

Recent experiments have challenged the endothelial expression of endosialin and suggested<br />

an expression by activated fibroblasts and pericytes. Subsequent studies have<br />

also confirmed that endosialin is upregulated in blood vessels in wide range of tumors<br />

and its expression is restricted to capillaries, which means that endosialin is probably<br />

involved in vascular reorganisation. It has been functionally implicated in angiogenesis,<br />

a process characterized by vascular branching and sprouting, which is necessary for tumor<br />

expansion and progression. In this work, we generated monoclonal antibodies against<br />

endosialin, characterized their isotypes and binding epitopes. We also analysed the<br />

activity of antibodies in a set of imunological assays and characterized the most stabile<br />

antibody VIII-16 with potential usage in next studies of endosialin function.<br />

Acknowledgements: This work was supported by VEGA 2/0210/09 and TRANSMED.<br />

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

153

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