In vivo expression of survivin and its splice variant survivin-2B: Impact on clinical outcome in acute myeloid leukemia
Autor: | Ingo Tamm, Christian Wuchter, Bernd Dörken, Mandy Wagner, Karin Schmelz, Wolf-Dieter Ludwig |
---|---|
Rok vydání: | 2006 |
Předmět: |
Adult
Male Cancer Research Survivin Apoptosis Biology Inhibitor of apoptosis Disease-Free Survival Immunophenotyping Inhibitor of Apoptosis Proteins In vivo Gene expression Humans splice RNA Messenger neoplasms Aged Neoplasm Staging Myeloid leukemia DNA Neoplasm Middle Aged Prognosis Neoplasm Proteins Alternative Splicing Oncology Leukemia Myeloid Case-Control Studies Acute Disease Immunology Cancer research Female Microtubule-Associated Proteins |
Zdroj: | International Journal of Cancer. 119:1291-1297 |
ISSN: | 1097-0215 0020-7136 |
Popis: | Survivin, a member of the inhibitor of apoptosis protein family, is expressed in most human cancers, but undetectable in normal differentiated adult tissue in vivo. Because of this cancer-related expression, survivin is a promising target for cancer therapy. To determine the expression and prognostic role of survivin in acute myeloid leukemia (AML), we investigated the mRNA expression pattern of survivin and of the splice variants survivin-2B and survivin-DeltaEx3 in adult (n = 74) and children (n = 31) with de novo AML using RT-PCR. Survivin was the predominant transcript variant in AML cells, whereas significantly lower levels of survivin-2B and survivin-DeltaEx3 were observed (p < or = 0.0001). Neither expression of survivin nor of any splice variant correlated with maturation stage (FAB subtypes, immunophenotype) or cytogenetic risk groups. For AML cases treated according to AMLCG92 (adult) and AML-BFM93 (children) protocols, respectively, expression patterns were correlated with clinical data: in adult AML (n = 51), low expression of survivin-2B correlated with a better overall survival (p = 0.05; mean survival time 19 months vs. 9 months) and a better eventfree survival (p < or = 0.01; 27 months vs. 10 months). In childhood AML (n = 31), high survivin-DeltaEx3 expression was associated with a shorter overall survival (p < or = 0.05; 24 months vs. 43 months). We conclude that certain survivin splice variants have potential prognostic impact for long-term therapy outcome in adult as well as childhood de novo AML. |
Databáze: | OpenAIRE |
Externí odkaz: |