Detailed Information on Publication Record
2010
Determination of Metallothionein in prostate tumor cell lines
GUMULEC, Jaromír, Michal MASAŘÍK, Šárka KUCHTÍČKOVÁ, Veronika KUDLÁČKOVÁ, Michal JURAJDA et. al.Basic information
Original name
Determination of Metallothionein in prostate tumor cell lines
Name in Czech
Stanovení metalothioneinu v liniích karcinomu prostaty
Authors
GUMULEC, Jaromír, Michal MASAŘÍK, Šárka KUCHTÍČKOVÁ, Veronika KUDLÁČKOVÁ, Michal JURAJDA, Dušan PAVLÍK, Arne ROVNÝ, Roman HRABEC, Soňa KŘÍŽKOVÁ and René KIZEK
Edition
XIV. Setkání biochemiků a molekulárních biologů, 2010
Other information
Language
English
Type of outcome
Konferenční abstrakt
Field of Study
30200 3.2 Clinical medicine
Country of publisher
Czech Republic
Confidentiality degree
není předmětem státního či obchodního tajemství
References:
Organization unit
Faculty of Medicine
ISBN
978-80-210-5164-5
Keywords (in Czech)
metalothionein;karcinom prostaty;nádorový marker;zinek
Keywords in English
metalothionein;prostate cancer;tumor marker;zinc;
Změněno: 29/11/2010 00:35, doc. MUDr. Jaromír Gumulec, Ph.D.
V originále
Prostate carcinoma (PCa) is the most common tumor and second leading cause of death due to cancer of men. Proteins such as metallothionein (MT) or alpha-methyl-CoA-racemase (AMACR) are highly overexpressed in prostate carcinoma. Althrough the role of these proteins in tumour tissue remains still unclear, it fulfills the requirements of higher specificity, which AMACR achieves at almost 100%. We have analyzed both proteins from prostate cancer cell lines LNCaP, PC-3 and 22RVL, compared to healthy prostate cell line PNT1A and then from PCa patients' serum compared to healthy serum controls. We've used immunohistochemical analysis, immunoprecipitation with magnetic nanoparticles, PAGE and dot blots. In all of these methods, we've found significant increase of expression in these samples.
In Czech
Metalothionein (MT) a alpha-methyl-CoA-racemáza (AMACR) jsou výrazně exprimovány u karcinomu prostaty s velkou mírou specifity pro toto onemocnění. Tyto proteiny byly analyzovány u buněčných linií LNCaP, PC-3 a 22RVL a PNT1A a ve vzorcích sér pacientů. Bylo použito imunohistochemických metod, imonoprecipitace s magnetickými nanočásticemi, SDS-PAGE a dot bloty.
Links
GP301/09/P436, research and development project |
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NS10200, research and development project |
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