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

  • J. H. Song
  • , S. H. Kweon
  • , H. J. Kim
  • , T. H. Lee
  • , W. S. Min
  • , H. J. Kim
  • , Y. K. Kim
  • , S. Y. Hwang
  • , T. S. Kim*
  • *Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    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.

    Original languageEnglish
    Pages (from-to)108-115
    Number of pages8
    JournalBritish Journal of Cancer
    Volume107
    Issue number1
    DOIs
    Publication statusPublished - 2012 Jun 26

    Bibliographical note

    Funding Information:
    This study was supported by the grant A111218-GM06 of the National Project for Personalized Genomic Medicine, Ministry for Health & Welfare and the National Research Foundation of Korea (NRF) grant 2011-0001388 funded by the Korea government.

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • AML
    • prognosis
    • standard chemotherapy
    • topoisomerase 2

    ASJC Scopus subject areas

    • Oncology
    • Cancer Research

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