BARCODE-ALL: accelerated and cost-effective genetic risk stratification in acute leukemia using spectrally addressable liquid bead microarrays

被引:13
作者
Wallace, J
Zhou, Y
Usmani, GN
Reardon, M
Newburger, P
Woda, B
Pihan, G
机构
[1] Univ Massachusetts, Sch Med, Lab Mol Diagnost, Worcester, MA USA
[2] Umass Mem Hlth Care, Worcester, MA USA
[3] Univ Massachusetts, Sch Med, Lab Hematopathol, Worcester, MA USA
[4] Univ Massachusetts, Sch Med, Dept Pathol, Worcester, MA USA
[5] Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA USA
关键词
microarray; lymphoblastic leukemia; risk stratification; RT-PCR;
D O I
10.1038/sj.leu.2402985
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
An increasing number of risk-stratifying genetic lesions in acute leukemia are being discovered and characterized. To translate this important and increasing volume of information from the research laboratory into effective clinical care, however, new, fast and comprehensive assays are needed. Toward this end, we have developed a two-stage multiplexing assay of broad applicability, which combines multiplex polymerase chain reaction with multiplex detection on spectrally addressable liquid bead microarrays. Using pediatric lymphoblastic leukemia as a model system, we demonstrate that all seven of the fusion transcripts resulting from risk-stratifying chromosomal translocations can be assayed in a single well of a 96-well multiplate with 100% specificity and sensitivity, within 6 h of specimen collection. The assay is automatic and high throughput and represents a significant improvement over previously available assays targeting the same genetic changes. We conclude that user-defined assays that multiplex both target selection and detection may have broad applicability in the management of hematological malignancies.
引用
收藏
页码:1404 / 1410
页数:7
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