Variant of ETV6/ABL1 gene is associated with leukemia phenotype

  • Joonhong Park
  • , Myungshin Kim
  • , Jihyang Lim
  • , Yonggoo Kim
  • , Kyungja Han
  • , Jae Seok Kim
  • , Seok Lee
  • , Hee Je Kim
  • , Woo Sung Min

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

The ETV6/ABL1 fusion transcript is thought to be a very rare aberration in hematopoietic malignancies. We describe two new cases of acute leukemia with the ETV6/ABL1 fusion, acute myeloid leukemia with eosinophilia (case 1) and B acute lymphoblastic leukemia (ALL) (case 2), screened by multiplex RT-PCR. The ETV6/ABL1 fusion was also confirmed by fluorescence in situ hybridization using a mixture of BCR/ABL1 and ETV6/RUNX1 probes. A thorough review of all published cases showed that all 7 reported ALL patients possess the type A ETV6/ABL1 fusion transcript, composed of the first 4 exons of ETV6 fused to the second exon of ABL1. The presence of the type A fusion transcript strongly implies ALL manifestation in ETV6/ABL1-positive hematologic malignancies as minor BCR breakpoint in BCR/ABL1-positive ALL.

Original languageEnglish
Pages (from-to)78-82
Number of pages5
JournalActa Haematologica
Volume129
Issue number2
DOIs
StatePublished - 2013

Keywords

  • Cryptic insertion
  • Eosinophilia
  • ETV6/ABL1 fusion
  • Exon 5 of ETV6

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