TY - JOUR
T1 - Chronic eosinophilic leukemia, NOS with t(5;12)(q31;p13)/ETV6-ACSL6 gene fusion
T2 - A novel variant of myeloid proliferative neoplasm with eosinophilia
AU - Su, Ruijun Jeanna
AU - Jonas, Brian A.
AU - Welborn, Jeanna
AU - Gregg, Jeffrey Paul
AU - Chen, Mingyi
N1 - Funding Information:
The study was partially support by Collaborative Institutional Research Pilot Grant for Investigators in Oncology, the Cancer Research Coordinating Committee (CRCC) and academic senate grants from University of California (MC) and NIH K12 CA138464 (BAJ). We thank Dr. Ralph Green for critical reading this manuscript.
Publisher Copyright:
© 2016 The Authors
PY - 2016/9/1
Y1 - 2016/9/1
N2 - The 2008 World Health Organization (WHO) classification of tumors of hematopoietic and lymphoid tissues introduced a category for myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1. Many of these patients are responsive to tyrosine kinase inhibitor (TKI) therapy. In this case report, we report a unique case of chronic eosinophilic leukemia with novel t(5;12)(q23-31;p13)/ETV6-ACSL6 gene fusion, in which patient was resistant to TKI therapy. This important finding is a novel addition to the above entity in WHO 2008 classification. The ACSL6 gene encodes a long-chain acyl-CoA synthetase, an enzyme that plays an essential role in lipid metabolism and ATP generation pathways in cells. The ETV6-ACSL6 rearrangement is present in diverse types of hematopoietic malignancies. As yet, it is not clear how ACSL6, a gene involved in fatty acid synthesis, contributes to clonal expansion of myeloid progenitor cells. Therefore, elucidating the contribution of ACSL6 to leukemogenesis may allow the development of novel treatment for those resistant to TKI therapy.
AB - The 2008 World Health Organization (WHO) classification of tumors of hematopoietic and lymphoid tissues introduced a category for myeloid and lymphoid neoplasms with eosinophilia and abnormalities of PDGFRA, PDGFRB or FGFR1. Many of these patients are responsive to tyrosine kinase inhibitor (TKI) therapy. In this case report, we report a unique case of chronic eosinophilic leukemia with novel t(5;12)(q23-31;p13)/ETV6-ACSL6 gene fusion, in which patient was resistant to TKI therapy. This important finding is a novel addition to the above entity in WHO 2008 classification. The ACSL6 gene encodes a long-chain acyl-CoA synthetase, an enzyme that plays an essential role in lipid metabolism and ATP generation pathways in cells. The ETV6-ACSL6 rearrangement is present in diverse types of hematopoietic malignancies. As yet, it is not clear how ACSL6, a gene involved in fatty acid synthesis, contributes to clonal expansion of myeloid progenitor cells. Therefore, elucidating the contribution of ACSL6 to leukemogenesis may allow the development of novel treatment for those resistant to TKI therapy.
KW - Chronic eosinophilic leukemia
KW - Myeloid proliferative neoplasm with eosinophilia
KW - NOS
KW - Novel ETV6-ACSL6 gene fusion
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U2 - 10.1016/j.ehpc.2015.10.001
DO - 10.1016/j.ehpc.2015.10.001
M3 - Article
C2 - 27458550
AN - SCOPUS:84995545982
SN - 2214-3300
VL - 5
SP - 6
EP - 9
JO - Human Pathology: Case Reports
JF - Human Pathology: Case Reports
ER -