Correlation analysis of p53 protein isoforms with NPM1/FLT3 mutations and therapy response in acute myeloid leukemia

N. Ånensen, S. M. Hjelle, W. Van Belle, I. Haaland, E. Silden, J.-C. Bourdon, R. Hovland, K. Taskén, S. Knappskog, P.E. Lønning, O. Bruserud, B. T. Gjertsen

    Research output: Contribution to journalArticle

    42 Citations (Scopus)

    Abstract

    The wild-type tumor-suppressor gene TP53 encodes several isoforms of the p53 protein. However, while the role of p53 in controlling normal cell cycle progression and tumor suppression is well established, the clinical significance of p53 isoform expression is unknown. A novel bioinformatic analysis of p53 isoform expression in 68 patients with acute myeloid leukemia revealed distinct p53 protein biosignatures correlating with clinical outcome. Furthermore, we show that mutated FLT3, a prognostic marker for short survival in AML, is associated with expression of full-length p53. In contrast, mutated NPM1, a prognostic marker for long-term survival, correlated with p53 isoforms ? and ? expression. In conclusion, p53 biosignatures contain useful information for cancer evaluation and prognostication. © 2012 Macmillan Publishers Limited All rights reserved.
    Original languageEnglish
    Pages (from-to)1533-1545
    Number of pages13
    JournalOncogene
    Volume31
    Issue number12
    DOIs
    Publication statusPublished - 2012

    Cite this

    Ånensen, N., Hjelle, S. M., Van Belle, W., Haaland, I., Silden, E., Bourdon, J-C., Hovland, R., Taskén, K., Knappskog, S., Lønning, P. E., Bruserud, O., & Gjertsen, B. T. (2012). Correlation analysis of p53 protein isoforms with NPM1/FLT3 mutations and therapy response in acute myeloid leukemia. Oncogene, 31(12), 1533-1545. https://doi.org/10.1038/onc.2011.348