Su Ruijun Jeanna, Jonas Brian A, Welborn Jeanna, Gregg Jeffrey Paul, Chen Mingyi
Department of Pathology and Laboratory Medicine, University of California at Davis Medical Center, Sacramento, CA 95817.
Division of Hematology and Oncology, University of California at Davis Medical Center, Sacramento, CA 95817.
Hum Pathol (N Y). 2016 Sep;5:6-9. doi: 10.1016/j.ehpc.2015.10.001.
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 , we report a unique case of chronic eosinophlic 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 EBV6-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.
2008年世界卫生组织(WHO)造血与淋巴组织肿瘤分类引入了一类伴有嗜酸性粒细胞增多以及血小板衍生生长因子受体α(PDGFRA)、血小板衍生生长因子受体β(PDGFRB)或成纤维细胞生长因子受体1(FGFR1)异常的髓系和淋巴系肿瘤。这些患者中的许多人对酪氨酸激酶抑制剂(TKI)治疗有反应。在此,我们报告一例独特的慢性嗜酸性粒细胞白血病病例,其具有新的t(5;12) (q23-31;p13)/ETV6-ACSL6基因融合,该患者对TKI治疗耐药。这一重要发现是对WHO 2008分类中上述实体的新补充。ACSL6基因编码一种长链酰基辅酶A合成酶,该酶在细胞的脂质代谢和ATP生成途径中起重要作用。EBV6-ACSL6重排在多种类型的造血恶性肿瘤中存在。目前尚不清楚参与脂肪酸合成的基因ACSL6如何促进髓系祖细胞的克隆扩增。因此,阐明ACSL6在白血病发生中的作用可能有助于开发针对TKI治疗耐药患者的新疗法。