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

Authors
Song, J. H.Kweon, S. H.Kim, H-JLee, T-HMin, W-SKim, H-JKim, Y-KHwang, S. Y.Kim, T. S.
Issue Date
26-6월-2012
Publisher
NATURE PUBLISHING GROUP
Keywords
AML; standard chemotherapy; prognosis; topoisomerase 2
Citation
BRITISH JOURNAL OF CANCER, v.107, no.1, pp.108 - 115
Indexed
SCIE
SCOPUS
Journal Title
BRITISH JOURNAL OF CANCER
Volume
107
Number
1
Start Page
108
End Page
115
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/108137
DOI
10.1038/bjc.2012.206
ISSN
0007-0920
Abstract
BACKGROUND: 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. METHODS: 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. RESULTS: 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). CONCLUSION: 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. British Journal of Cancer (2012) 107, 108-115. doi: 10.1038/bjc.2012.206 www.bjcancer.com Published online 24 May 2012 (C) 2012 Cancer Research UK
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