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High TOP2B/TOP2A expression ratio at diagnosis correlates with favourable outcome for standard chemotherapy in acute myeloid leukaemia.

Authors :
Song JH
Kweon SH
Kim HJ
Lee TH
Min WS
Kim YK
Hwang SY
Kim TS
Song, J H
Kweon, S H
Kim, H-J
Lee, T-H
Min, W-S
Kim, Y-K
Hwang, S Y
Kim, T S
Source :
British Journal of Cancer. 6/26/2012, Vol. 107 Issue 1, p108-115. 8p.
Publication Year :
2012

Abstract

<bold>Background: </bold>Cytosine arabinoside-based chemotherapy coupled with anthracycline is currently the first-line treatment for acute myeloid leukaemia (AML), but diverse responses to the regimen constitute obstacles to successful treatment. Therefore, outcome prediction to chemotherapy at diagnosis is believed to be a critical consideration.<bold>Methods: </bold>The mRNA expression of 12 genes closely involved in the actions of cytosine arabinoside and anthracycline was evaluated by real-time reverse transcriptase PCR (RT-PCR), in 54 diagnostic bone marrow specimens of M2-subtype AML.<bold>Results: </bold>Low expression levels of ribonucleotide reductase M2 (RRM2) and high expression levels of topoisomerase 2 beta (TOP2B) were correlated with longer survival in a univariate analysis. Another interesting finding is that high ratios of TOP2B/RRM2 and TOP2B/TOP2 alpha (TOP2A) in a combined analysis were also shown to have a prognostic impact for longer survival with improved accuracy. Among the four markers, when adjusted for the influence of other clinical factors in multivariate analysis, the TOP2B/TOP2A ratio was significantly correlated with treatment outcomes; patients with high ratios trended toward longer disease-free survival (HR, 0.24; P=0.002) and overall survival (HR, 0.29; P=0.005).<bold>Conclusion: </bold>Genes with distinct expression profiles such as TOP2B/TOP2A expression ratio at diagnosis can be employed for outcome prediction after the treatment with standard regimens in AML patients with M2 subtype. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00070920
Volume :
107
Issue :
1
Database :
Academic Search Index
Journal :
British Journal of Cancer
Publication Type :
Academic Journal
Accession number :
104444250
Full Text :
https://doi.org/10.1038/bjc.2012.206