OLTOVÁ, Alexandra, Petra ŠMUHAŘOVÁ, Petr KUGLÍK, Dita ŽEŽULKOVÁ, Vladimíra VRANOVÁ, Peter MÚDRY, Věra BAIČIOVÁ and Jaroslav ŠTĚRBA. Detection of chromosomal aberrations by FISH, CGH and SKY in cultured and noncultured tumours in children during 2003 and 2005. In Europen Journal of Human Genetics. Amsterdam: ESHG, 2006, p. 226. ISBN 80-7232-264-8.
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Basic information
Original name Detection of chromosomal aberrations by FISH, CGH and SKY in cultured and noncultured tumours in children during 2003 and 2005
Name in Czech Detekce chromozomových aberací u kultivovaných a nekultivovaných dětských solidních nádorů pomocí techniky FISH, CGH a SKY v průběhu let 2003 až 2005
Authors OLTOVÁ, Alexandra (203 Czech Republic), Petra ŠMUHAŘOVÁ (203 Czech Republic), Petr KUGLÍK (203 Czech Republic, guarantor), Dita ŽEŽULKOVÁ (203 Czech Republic), Vladimíra VRANOVÁ (703 Slovakia), Peter MÚDRY (203 Czech Republic), Věra BAIČIOVÁ (203 Czech Republic) and Jaroslav ŠTĚRBA (203 Czech Republic).
Edition Amsterdam, Europen Journal of Human Genetics, p. 226-226, 2006.
Publisher ESHG
Other information
Original language English
Type of outcome Proceedings paper
Field of Study Genetics and molecular biology
Country of publisher United Kingdom of Great Britain and Northern Ireland
Confidentiality degree is not subject to a state or trade secret
RIV identification code RIV/00216224:14310/06:00017836
Organization unit Faculty of Science
ISBN 80-7232-264-8
Keywords in English Chromosomal aberrations; solid tumours in children; FISH; CGH; SKY
Tags CGH, chromosomal aberrations, FISH, SKY, solid tumours in children
Changed by Changed by: prof. MUDr. Jaroslav Štěrba, Ph.D., učo 348. Changed: 23/3/2010 12:28.
Abstract
Pediatric tumors are the second main cause of childrens death in developed countries. Contrary to leukemias chromosomal alterations associated with malignant transformations are less well characterized for pediatric solid tumors. We present results of cytogenetic examinations of 262 pediatric solid tumors. Some of them were examined using by interphase fluorescent in situ hybridization (I-FISH), especially tumors where deletions or amplifications of specific genes and/or presence of fusion genes are known and could be used as diagnostic tool. Proven prognostic significance of the n-myc amplification, del 1p36, gain 17q, abnormalities on chromosome 11 are well known for children with neuroblastoma. For medulloblastomas i(17p), c-myc and i(12p) in germinal tumors are the other candidates. Vast majority of tumor samples were cultured and other possible chromosomal abnormalities were detected using FISH, spectral karyotyping (SKY) and comparative genomic hybridization (CGH). During last few months we have applied also high-resolution comparative genomic hybridization (HR-CGH). Cultivation of solid tumor tissue is not always successful, possible explanation could be generally low proliferation activity of tumor cells in vitro. Here we present our cytogenetic results together with clinical characteristics.
Abstract (in Czech)
Práce se zabývá detekcí chromozomových aberací ve vzorcích kultivované a nekultivované tkáně solidních dětských nádorů pomocí techniky FISH, CGH a spektrálního karyotypování (SKY) Jsou zhodnoceny cytogenetické nálezy u pacientů léčených na KDO FN Brno v letech 2003-2005.
Links
MSM0021622415, plan (intention)Name: Molekulární podstata buněčných a tkáňových regulací
Investor: Ministry of Education, Youth and Sports of the CR, Molecular basis of cell and tissue regulations
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