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早期造血祖细胞参与急性早幼粒细胞白血病的证据。

Evidence for early hematopoietic progenitor cell involvement in acute promyelocytic leukemia.

作者信息

Edwards R H, Wasik M A, Finan J, Rodriguez R, Moore J, Kamoun M, Rennert H, Bird J, Nowell P C, Salhany K E

机构信息

Department of Pathology and Laboratory Medicine, Cancer Center Flow Cytometry and Cell Sorting Facility, Philadelphia, USA.

出版信息

Am J Clin Pathol. 1999 Dec;112(6):819-27. doi: 10.1093/ajcp/112.6.819.

Abstract

Acute promyelocytic leukemia (APL) represents a subtype of acute myeloid leukemia with characteristic morphologic, molecular, and immunophenotypic features. Previous immunophenotypic analyses have shown that leukemic cells in APL typically express the myeloid markers CD33 and CD13 but lack expression of the early hematopoietic progenitor cell antigens CD34 and HLA-DR. We analyzed selected immunophenotypic features of APL by flow cytometry and showed that 7 (41%) of 17 cases contained significant subsets of CD34+ leukemic cells: CD34+ myeloid cells predominated in 2 APL cases. By using a fluorescence-activated cell sorter-fluorescence in situ hybridization approach, we confirmed that the CD34+ cells harbored the t(15;17) translocation characteristic of APL. By using the same experimental approach, CD34+ populations were stratified into primitive CD34+ CD38- and committed CD34+ CD38+ progenitor cell subpopulations; cells in both subsets contained the t(15;17) translocation. The knowledge that APL may be partly or largely CD34+ is important for proper diagnosis. Furthermore, identification of the t(15;17) translocation in CD34+ CD38- blasts indicates that, in at least some cases, the leukemogenic mutation in APL occurs within primitive hematopoietic progenitor cells.

摘要

急性早幼粒细胞白血病(APL)是急性髓系白血病的一种亚型,具有独特的形态学、分子学和免疫表型特征。既往免疫表型分析显示,APL中的白血病细胞通常表达髓系标志物CD33和CD13,但缺乏早期造血祖细胞抗原CD34和HLA-DR的表达。我们通过流式细胞术分析了APL的选定免疫表型特征,结果显示,17例中有7例(41%)含有显著的CD34+白血病细胞亚群:2例APL病例中以CD34+髓系细胞为主。通过使用荧光激活细胞分选仪-荧光原位杂交方法,我们证实CD34+细胞具有APL特征性的t(15;17)易位。通过使用相同的实验方法,CD34+群体被分层为原始CD34+ CD38-和定向CD34+ CD38+祖细胞亚群;两个亚群中的细胞均含有t(15;17)易位。APL可能部分或大部分为CD34+这一认识对正确诊断很重要。此外,在CD34+ CD38-原始细胞中鉴定出t(15;17)易位表明,至少在某些情况下,APL中的致白血病突变发生在原始造血祖细胞内。

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