## Abstract In this report, we describe an inflammatory myofibroblastic tumor (IMT) of the urinary bladder in a 46‐year‐old man. Tumor cells presented striking cytoplasmatic ALK immunopositivity. Cytogenetic and FISH analysis, by use of a multicolor chromosome 2 banding probe, revealed a 46,XY,der(
Fusion of the SEC31L1 and ALK genes in an inflammatory myofibroblastic tumor
✍ Scribed by Ioannis Panagopoulos; Therese Nilsson; Henryk A. Domanski; Margareth Isaksson; Pia Lindblom; Fredrik Mertens; Nils Mandahl
- Publisher
- John Wiley and Sons
- Year
- 2005
- Tongue
- French
- Weight
- 425 KB
- Volume
- 118
- Category
- Article
- ISSN
- 0020-7136
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✦ Synopsis
Abstract
Inflammatory myofibroblastic tumor (IMT) is a neoplasm composed of myofibroblastic spindle cells and infiltrating inflammatory cells. Cytogenetic analyses have revealed that a subgroup of IMT, in particular among children and young adults, harbors clonal chromosomal rearrangements involving chromosome band 2p23. Further, molecular genetic studies have shown that these rearrangements target the ALK gene, serving as the 3′‐partner in fusion genes with various translocation partners. In the present study, we describe the finding of a novel SEC31L1/ALK fusion gene in an intraabdominal IMT of a young man. G‐band analysis revealed a translocation t(2;4)(p23;q21) and subsequent fluorescence in situ hybridization with locus‐specific probes strongly indicated disruption of the ALK locus on chromosome 2. Immunostaining with monoclonal mouse anti‐human CD246 ALK Protein showed diffuse cytoplasmic positivity. Using reverse primers for the __ALK‐__gene, we could, by 5′‐RACE methodology, amplify a single 1.2 kb fragment. Sequence analysis showed that the fragment was a hybrid cDNA product in which nt 3012 of SEC31L1 (NM_016211), located in band 4q21, was fused in‐frame to nt 4080 of ALK (NM_004304). RT‐PCR with two sets of primer pairs specific for SEC31L1 and ALK amplified two transcripts, which at sequencing corresponded to two types of chimeric SEC31L1/ALK transcripts. In the long, type I, transcript nt 3012 of SEC31L1 (NM_016211) was fused in‐frame to nt 4080 of ALK. In the short, type II, transcript nt 2670 of SEC31L1 was fused in‐frame to nt 4080 of ALK. Genomic PCR and subsequent sequencing showed that the breakpoints were located in intron 23 of SEC31L1 and intron 20 of ALK. © 2005 Wiley‐Liss, Inc.
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