Atypical mRNA Fusions in PML-RARA Positive, RARA-PML Negative Acute Promyelocytic Leukemia

被引:20
作者
Walz, Christoph [1 ,2 ]
Grimwade, David [3 ]
Saussele, Susanne [1 ]
Lengfelder, Eva [1 ]
Haferlach, Claudia [4 ]
Schnittger, Susanne [4 ]
Lafage-Pochitaloff, Marina [5 ,6 ]
Hochhaus, Andreas [1 ,7 ]
Cross, Nicholas C. P. [8 ]
Reiter, Andreas [1 ]
机构
[1] Univ Med Mannheim, Med Klin 3, D-68167 Mannheim, Germany
[2] Univ Med Mannheim, Inst Pathol, D-68167 Mannheim, Germany
[3] Kings Coll London, Dept Med & Mol Genet, Sch Med, London WC2R 2LS, England
[4] Munchner Leukamie Labor, Munich, Germany
[5] CHU Timone, AP HM, Dept Genet, Marseille, France
[6] Univ Mediterranee, Marseille, France
[7] Univ Klinikum Jena, Dept Hematol Oncol, Jena, Germany
[8] Univ Southampton, Salisbury & Human Genet Div, Wessex Reg Genet Lab, Salisbury, Wilts, England
关键词
SUBMICROSCOPIC DELETIONS; ALPHA-PML; T(15/17); TRANSLOCATIONS; VARIANT; HYBRIDIZATION; PENETRANCE; EXPRESSION; RESISTANCE; ISOFORM;
D O I
10.1002/gcc.20757
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Reciprocal RARA-PML transcripts are not detected in similar to 25% of patients with PML-RARA positive acute promyelocytic leukemia (APL), but the reasons for this are poorly understood. We studied 21 PML-RARA positive/RARA-PML negative cases by bubble PCR and multiplex long template PCR to identify the genomic breakpoints. Additional RT-PCR analysis was performed based on the DNA findings. Three cases were found to have complex rearrangements involving a third locus: the first had a PML-CDC6-RARA forward DNA fusion and expressed a chimeric PML-CDC6-RARA mRNA in addition to a PML-RARA. The other two had HERCI-PML and NT_00974.17-PML genomic fusion sequences at their respective reciprocal breakpoints. Six patients were falsely classified as RARA-PML negative due to deletions on chromosome 15 and/or 17, or alternative splicing leading to atypical RARA-PML fusion transcripts, which were not identified by conventional RT-PCR assays. This study demonstrates that the frequency of RARA-PML expression has been underestimated and highlights remarkable complexity at chromosomal breakpoint regions in APL even in cases with an apparently simple balanced t(15;17)(q24;q12). (C) 2010 Wiley-Liss, Inc.
引用
收藏
页码:471 / 479
页数:9
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