Molecular analysis of t(11;19) breakpoints in childhood acute leukemias

被引:50
作者
Rubnitz, JE
Behm, FG
CurcioBrint, AM
Pinheiro, VRP
Carroll, AJ
Raimondi, SC
Shurtleff, SA
Downing, JR
机构
[1] ST JUDE CHILDRENS RES HOSP, DEPT HEMATOL ONCOL, MEMPHIS, TN 38105 USA
[2] ST JUDE CHILDRENS RES HOSP, DEPT PATHOL & LAB MED, MEMPHIS, TN 38105 USA
[3] ST JUDE CHILDRENS RES HOSP, DEPT TUMOR CELL BIOL, MEMPHIS, TN 38105 USA
[4] UNIV TENNESSEE, COLL MED, DEPT PATHOL, MEMPHIS, TN USA
[5] UNIV TENNESSEE, COLL MED, DEPT PEDIAT, MEMPHIS, TN USA
[6] UNIV ALABAMA, MED GENET LAB, BIRMINGHAM, AL 35294 USA
关键词
D O I
10.1182/blood.V87.11.4804.bloodjournal87114804
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
MLL is fused to ENL or ELL in acute leukemias that contain t(11;19)(q23;p13). Although ENL and ELL localize to chromosome 19, bands p13.3 and p13.1, respectively, these breakpoints are not always readily distinguished by standard cytogenetics. We therefore used reverse transcriptase-polymerase chain reaction (RT-PCR) assays to analyze 26 cases of childhood acute leukemia containing t(11;19) to determine the frequencies of ENL and ELL involvement. All 17 cases of acute lymphoblastic leukemia (ALL) had MLL/ENL fusion transcripts. By contrast, of the 9 cases of acute myeloid leukemia (AML) analyzed, 6 had MLL/ENL fusions, 2 had MLL/ELL fusions, and 1 case had no RT-PCR-detectable MLL fusion mRNA. These data suggest that the majority of 11;19 translocations involve ENL, whereas involvement of ELL is relatively uncommon in childhood acute leukemia and may be restricted to AML. (C) 1996 by The American Society of Hematology.
引用
收藏
页码:4804 / 4808
页数:5
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