Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma
Cell Leukemia

a 2013

Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma Cell Leukemia

KRYUKOV, Fedor; Elena Vladimirovna DEMENTYEVA; Lenka KUBICZKOVÁ; Sabina ŠEVČÍKOVÁ; Jiří JARKOVSKÝ et. al.

Základní údaje

Originální název

Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma Cell Leukemia

Autoři

KRYUKOV, Fedor; Elena Vladimirovna DEMENTYEVA; Lenka KUBICZKOVÁ; Sabina ŠEVČÍKOVÁ; Jiří JARKOVSKÝ; Lucie BROŽOVÁ; Pavel NĚMEC; Lenka ZAHRADOVÁ; Luděk POUR a Roman HÁJEK

Vydání

14th International Myeloma Workshop, 2013

Další údaje

Jazyk

angličtina

Typ výsledku

Konferenční abstrakt

Obor

30200 3.2 Clinical medicine

Stát vydavatele

Spojené státy

Utajení

není předmětem státního či obchodního tajemství

Impakt faktor

Impact factor: 1.929

Organizační jednotka

Lékařská fakulta

ISSN

Změněno: 20. 5. 2013 12:32, Mgr. Anna Potáčová, Ph.D.

Anotace

V originále

The regulation of cell cycle is dynamic and is determined not by the absolute level of any regulator, but by the aggregate balance between positive/negative cell-cycle regulators and the interplay among them. The objective of study was to describe coexpression correlations of cell cycle regulatory genes in MM and PCL. Chosen genes, responsible for G1-to-S cell-cycle progression, were divided into 2 groups based on their regulatory role: activators and blockers. Comparison of gene expression (qRT-PCR) in MM and PCL revealed up-regulation of CDKN2A (2.7-fold change, p=0.045) and CCND1 (7.9-fold change, p=0.005) in PCL samples. In PCL cohort, CCND1 and CDK6 expression lost correlation with blocker genes and CDKN1B expression lost correlation with activator genes. For CDKN2A and CDKN1A blocker genes loss of correlation with some activators were associated with significant increasing of correlation with other ones. Such reaction can be explained by compensation mechanisms. Univariate Cox proportional hazards survival model with one explanatory variable showed prognostic impact for CDKN2A (HR 1.022 [HR95%CI: 1.004; 1.040]; p=0.016) and CCND3 (HR 1.489 [HR95%CI: 1.112; 1.993]; p=0.008) in MM cohort. Thus, our data highlight changes in correlations between cell cycle blockers and activators during MM to PCL progression. Despite compensation mechanisms activation (CDKN2A, CDKN1A) whole regulatory complex seems to be imbalanced (CCND1, CDK6, CDKN1B), which can be explained by severe cell cycle dysregulation during progression to PCL.

Návaznosti

NT11154, projekt VaV

Název: Úloha mitotické disrupce v B lymfocytech u mnohočetném myelomu

Investor: Ministerstvo zdravotnictví ČR, Úloha mitotické disrupce v B lymfocytech u mnohočetného myelomu

NT13190, projekt VaV

Název: Molekulární charakteristika centrozomálních abnormalit a jejich prognostický význam pro pacienty s mnohočetným myelomem

Investor: Ministerstvo zdravotnictví ČR, Molekulární charakteristika centrozomálních abnormalit a jejich prognostický význam pro pacienty s mnohočetným myelomem

Citovat

KRYUKOV, Fedor; Elena Vladimirovna DEMENTYEVA; Lenka KUBICZKOVÁ; Sabina ŠEVČÍKOVÁ; Jiří JARKOVSKÝ; Lucie BROŽOVÁ; Pavel NĚMEC; Lenka ZAHRADOVÁ; Luděk POUR a Roman HÁJEK. Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma Cell Leukemia. In 14th International Myeloma Workshop. 2013. ISSN 2152-2650.

@proceedings{1107535,
   author = {Kryukov, Fedor and Dementyeva, Elena Vladimirovna and Kubiczková, Lenka and Ševčíková, Sabina and Jarkovský, Jiří and Brožová, Lucie and Němec, Pavel and Zahradová, Lenka and Pour, Luděk and Hájek, Roman},
   booktitle = {14th International Myeloma Workshop},
   language = {eng},
   title = {Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma Cell Leukemia},
   year = {2013}
}

TY  - CONF
ID  - 1107535
AU  - Kryukov, Fedor - Dementyeva, Elena Vladimirovna - Kubiczková, Lenka - Ševčíková, Sabina - Jarkovský, Jiří - Brožová, Lucie - Němec, Pavel - Zahradová, Lenka - Pour, Luděk - Hájek, Roman
PY  - 2013
TI  - Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma Cell Leukemia
N2  - The regulation of cell cycle is dynamic and is determined not by the absolute level of any regulator, but by the aggregate balance between positive/negative cell-cycle regulators and the interplay among them. The objective of study was to describe coexpression correlations of cell cycle regulatory genes in MM and PCL. Chosen genes, responsible for G1-to-S cell-cycle progression, were divided into 2 groups based on their regulatory role: activators and blockers. Comparison of gene expression (qRT-PCR) in MM and PCL revealed up-regulation of CDKN2A (2.7-fold change, p=0.045) and CCND1 (7.9-fold change, p=0.005) in PCL samples. In PCL cohort, CCND1 and CDK6 expression lost correlation with blocker genes and CDKN1B expression lost correlation with activator genes. For CDKN2A and CDKN1A blocker genes loss of correlation with some activators were associated with significant increasing of correlation with other ones. Such reaction can be explained by compensation mechanisms. Univariate Cox proportional hazards survival model with one explanatory variable showed prognostic impact for CDKN2A (HR 1.022 [HR95%CI: 1.004; 1.040]; p=0.016) and CCND3 (HR 1.489 [HR95%CI: 1.112; 1.993]; p=0.008) in MM cohort. Thus, our data highlight changes in correlations between cell cycle blockers and activators during MM to PCL progression. Despite compensation mechanisms activation (CDKN2A, CDKN1A) whole regulatory complex seems to be imbalanced (CCND1, CDK6, CDKN1B), which can be explained by severe cell cycle dysregulation during progression to PCL.
ER  -

KRYUKOV, Fedor; Elena Vladimirovna DEMENTYEVA; Lenka KUBICZKOVÁ; Sabina ŠEVČÍKOVÁ; Jiří JARKOVSKÝ; Lucie BROŽOVÁ; Pavel NĚMEC; Lenka ZAHRADOVÁ; Luděk POUR a Roman HÁJEK. Cell Cycle Genes Coexpression in Multiple Myeloma and Plasma Cell Leukemia. In \textit{14th International Myeloma Workshop}. 2013. ISSN~2152-2650.

Přehled o publikaci