PRAME is a membrane and cytoplasmic protein aberrantly expressed in chronic lymphocytic leukemia and mantle cell lymphoma

被引:33
作者
Proto-Siqueira, Rodrigo
Figueiredo-Pontes, Lorena L.
Panepucci, Rodrigo A.
Garcia, Aglair B.
Rizzatti, Edgar G.
Nascimento, Fabio M.
Ishikawa, Hellen C. F.
Larson, Roy E.
Falcao, Roberto P.
Simpson, Andrew J.
Gout, Ivan
Filonenko, Valery
Rego, Eduardo M.
Zago, Marco A.
机构
[1] Univ Sao Paulo, Med Sch Ribeirao Preto, Div Hematol, BR-05508 Sao Paulo, Brazil
[2] Univ Sao Paulo, Med Sch Ribeirao Preto, Ctr Cell Based Therapy, BR-05508 Sao Paulo, Brazil
[3] Univ Sao Paulo, Med Sch Ribeirao Preto, Dept Mol & Cellular Biol Pathogens, BR-05508 Sao Paulo, Brazil
[4] Ludwig Inst Canc Res, New York, NY USA
[5] NAS Ukraine, Inst Mol Biol & Genet, Kiev, Ukraine
[6] Ludwig Inst Canc Res, London W1P 8BT, England
基金
巴西圣保罗研究基金会;
关键词
PRAME; CLL; mantle cell lymphoma; quantitative flow cytometry;
D O I
10.1016/j.leukres.2006.02.031
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The preferentially expressed antigen in melanoma (PRAME) gene is aberrantly expressed in chronic lymphoproliferative disorders (CLD). We produced and characterized an anti-PRAME monoclonal antibody (MoAb), which was then applied in a quantitative flow cytometric (QFC) method to evaluate PRAME expression in leukemic cells from the peripheral blood (PB) of 47 patients with chronic lymphocytic leukemia and seven with mantle cell lymphoma as well as in the PB mononuclear cells (PBMCs) and B lymphocytes from 15 healthy subjects. Approximately 90% of CLD, but none of the normal samples, presented more than 20% of PRAME+ lymphocytes. Moreover, the intensity of PRAME expression was significantly higher in CLD cells compared to normal B lymphocytes and PBMCs. By immunofluorescence microscopy and by permeabilized flow cytometry we demonstrated that PRAME is a membrane antigen and a cytoplasmic protein aberrantly expressed in malignant CLD. Our results suggest that the analysis of PRAME protein may contribute for the distinction between normal and leukemic cells in CLD, and that PRAME may be a potential target for therapy. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1333 / 1339
页数:7
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