Publication Date:
2008-11-16
Description:
Identification and characterization of therapy-related acute myeloid leukemia (tAML) susceptibility factors could help distinguish between high- and low-risk patients and suggest logical targets for prevention and control strategies. Our lab recently identified the anti-apoptotic gene Bcl2 as a candidate tAML susceptibility gene based its proximity to a quantitative trait locus (QTL) peak (Mleu1.1) associated with time-to-leukemia in B6C3F1 × SWR/J F2 intercross mice treated with the potent alkylator N-ethyl-N-nitrosourea (ENU). Recent studies have shown that, in addition to its anti-apoptotic properties, Bcl2 decreases both mismatch repair activity and abasic site repair. Thus, higher Bcl2 expression levels in early hematopoietic cells at baseline or in response to chemotherapy could prevent both apoptosis and DNA repair in the affected cells, leading to the accumulation of potentially leukemogenic mutations in surviving cells. At Mleu1.1, mice homozygous for SWR/J alleles have longer survival compared to mice homozygous for the C57BL/6J haplotype. We hypothesized that Bcl2 could be the underlying QTL gene driving this phenotype, with higher Bcl2 expression predicted in C57BL/6J compared to SWR/J mice. Because early hematopoietic cells are implicated as the transforming population in tAML, we measured Bcl2 RNA expression in Lin−/c-Kit+ (enriched for stem/progenitors) sorted cells using the Illumina BeadChip Platform. Concordant with our hypothesis, Bcl2 expression measured by 3 separate probes was 43.0% (p=0.002), 44.5% (p=0.002), and 33.5% (p=0.06) lower in SWR/J compared to C57BL/6J (n=3 mice per strain). We then measured Bcl2 protein expression by flow cytometry in LSK (Lin−/Sca+/c-Kit+), CMP (Lin−/c-Kit+/Sca−/Fcγ −/CD34+), GMP (Lin−/c-Kit+/Sca−/Fcγ+/CD34+), and MEP (Lin−/c-Kit+/Sca−/Fcγ −/CD34−) cells. In C57BL/6J mice (n=3), 4.49±1.28%, 14.97±2.44%, 5.87±2.53%, and 8.86±1.81% of LSKs, CMPs, GMPs, and MEPs respectively were Bcl2 positive. Concordant with RNA expression data, a lower percentage of LSKs (p=0.02) from SWR/J mice (n=3) were Bcl2+. Specifically, we detected 1.70±0.31%, 13.43±2.87%, 6.09±1.96%, and 6.26±1.64% Bcl2+ LSKs, CMPs, GMPs, and MEPs respectively. To determine the effect of ENU exposure on Bcl2 expression, we treated mice (n=3 per strain) with 100 mg/kg ENU 24 hours prior to flow cytometric analysis. Compared to baseline, treated mice had decreased total bone marrow cellularity (13.0±4.1 × 106 vs. 28.1±6.8 × 106 viable cells recovered per mouse; treated vs. untreated) and increased percent Bcl2+ cells in most compartments of early hematopoiesis in both strains. However, the percent Bcl2+ cells from ENU treated mice was higher in C57BL/6J vs. SWR/J mice (p
Print ISSN:
0006-4971
Electronic ISSN:
1528-0020
Topics:
Biology
,
Medicine
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