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Cell cycle genes co-expression in multiple myeloma and plasma cell leukemia
Fedor Kryukov, Elena Dementyeva, Lenka Kubiczkova, Jiri Jarkovsky, Lucie Brozova, Jakub Petrik, Pavel Nemec, Sabina Sevcikova, Jiri Minarik, Zdena Stefanikova, Petr Kuglik, Roman Hajek
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT11154
MZ0
CEP - Centrální evidence projektů
NT12130
MZ0
CEP - Centrální evidence projektů
NT13190
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
Plný text - Článek
Plný text - Článek
Zdroj
Zdroj
Zdroj
NLK
Free Medical Journals
od 2006 do Před 18 měsíci
Elsevier Open Access Journals
od 2005-12-01
ROAD: Directory of Open Access Scholarly Resources
od 1987
Elsevier Open Archive Journals
od 2005-12-01 do Před 18 měsíci
- MeSH
- analýza přežití MeSH
- buněčný cyklus genetika MeSH
- časové faktory MeSH
- CDC geny * MeSH
- HeLa buňky MeSH
- inhibitor p16 cyklin-dependentní kinasy genetika metabolismus MeSH
- lidé středního věku MeSH
- lidé MeSH
- mnohočetný myelom diagnóza genetika MeSH
- nádorové buňky kultivované MeSH
- plazmocelulární leukemie diagnóza genetika MeSH
- prognóza MeSH
- progrese nemoci MeSH
- regulace genové exprese u nádorů MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- Check Tag
- lidé středního věku MeSH
- lidé MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
The objective of this study was to describe co-expression correlations of cell cycle regulatory genes in multiple myeloma (MM) and plasma cell leukemia (PCL). Our results highlight the presence of dynamic equilibrium between co-expression of activator and inhibitor gene sets. Moreover inhibitor set is more sensitive to the activator changes, not vice versa. We have shown that CDKN2A expression is associated with short-term survival in newly diagnosed MM patients (survival was 30.3 ± 3.9 months for 'low' expressed and 7.5 ± 5.6 months for 'high' expressed group, p<0.0001). Moreover low-expression CDKN2A group showed time-to-progression benefit in newly diagnosed patients (remission was 20.8 ± 3.6 months for 'low' and 8.4 ± 2.7 months for 'high' expressed group, p<0.0001) as well as in whole studied cohort of MM patients (remission was 20.8 ± 2.8 months for 'low' and 9.8 ± 1.1 months for 'high' expressed group, p<0.0001). The overexpression of inhibitors can be explained as a compensatory reaction to growing "oncogenic stress".
Department of Clinical Hematology University Hospital Brno Czech Republic
Department of Hematology and Blood Transfusion University Hospital Bratislava Slovak Republic
Institute of Biostatistics and Analyses Faculty of Medicine Masaryk University Brno Czech Republic
Instituteof Clinical Hematology University Hospital Ostrava Czech Republic
Citace poskytuje Crossref.org
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