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Genes Contributing to Minimal Residual Disease in Childhood Acute Lymphoblastic Leukemia: Prognostic Significance of CASP8AP2

Overview
Journal Blood
Publisher Elsevier
Specialty Hematology
Date 2006 Apr 22
PMID 16627760
Citations 42
Authors
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Abstract

In childhood acute lymphoblastic leukemia (ALL), early response to treatment is a powerful prognostic indicator. To identify genes associated with this response, we analyzed gene expression of diagnostic lymphoblasts from 189 children with ALL and compared the findings with minimal residual disease (MRD) levels on days 19 and 46 of remission induction treatment. After excluding genes associated with genetic subgroups, we identified 17 genes that were significantly associated with MRD. The caspase 8-associated protein 2 (CASP8AP2) gene was studied further because of its reported role in apoptosis and glucocorticoid signaling. In a separate cohort of 99 patients not included in the comparison of gene expression profiles and MRD, low levels of CASP8AP2 expression predicted a lower event-free survival (P = .02) and a higher rate of leukemia relapse (P = .01) and were an independent predictor of outcome. High levels of CASP8AP2 expression were associated with a greater propensity of leukemic lymphoblasts to undergo apoptosis. We conclude that measurement of CASP8AP2 expression at diagnosis offers a means to identify patients whose leukemic cells are highly susceptible to chemotherapy. Therefore, this gene is a strong candidate for inclusion in gene expression arrays specifically designed for leukemia diagnosis.

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References
1.
Pui C, Chessells J, Camitta B, Baruchel A, Biondi A, Boyett J . Clinical heterogeneity in childhood acute lymphoblastic leukemia with 11q23 rearrangements. Leukemia. 2003; 17(4):700-6. DOI: 10.1038/sj.leu.2402883. View

2.
Silverman L, Sallan S . Newly diagnosed childhood acute lymphoblastic leukemia: update on prognostic factors and treatment. Curr Opin Hematol. 2003; 10(4):290-6. DOI: 10.1097/00062752-200307000-00007. View

3.
Williams D, Tsiatis A, Brodeur G, Look A, Melvin S, Bowman W . Prognostic importance of chromosome number in 136 untreated children with acute lymphoblastic leukemia. Blood. 1982; 60(4):864-71. View

4.
Kumagai M, Manabe A, Pui C, Behm F, Raimondi S, Hancock M . Stroma-supported culture in childhood B-lineage acute lymphoblastic leukemia cells predicts treatment outcome. J Clin Invest. 1996; 97(3):755-60. PMC: 507113. DOI: 10.1172/JCI118474. View

5.
Imai Y, Kimura T, Murakami A, Yajima N, Sakamaki K, Yonehara S . The CED-4-homologous protein FLASH is involved in Fas-mediated activation of caspase-8 during apoptosis. Nature. 1999; 398(6730):777-85. DOI: 10.1038/19709. View