Lipoprotein lipase expression is a novel prognostic factor in B-cell chronic lymphocytic leukemia

被引:51
作者
Nueckel, Holger
Huettmann, Andreas
Klein-Hitpass, Ludger
Schroers, Roland
Fuehrer, Anja
Sellmann, Ludger
Duehrsen, Ulrich
Duerig, Jan
机构
[1] Univ Hosp Essen, Dept Hematol, D-45122 Essen, Germany
[2] Univ Duisburg Essen, Univ Hosp Essen, Inst Cell Biol, Essen, Germany
[3] Univ Gottingen, Dept Hematol & Oncol, D-3400 Gottingen, Germany
关键词
B-cell chronic lymphocytic leukemia (B-CLL); prognostic marker; LPL; ADAM29; protein tyrosine kinase; ZAP-70; CD38; antigen;
D O I
10.1080/10428190500464161
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
B-cell chronic lymphocytic leukemia (B-CLL) is a heterogenous disease with a highly variable clinical course. Recent studies have shown that expression of lipoprotein lipase (LPL) and ADAM29 may serve as novel prognostic markers in B-CLL. To investigate the prognostic value of these genes, we quantified their expression in peripheral blood mononuclear cells using quantitative reverse transcriptase-polymerase chain reaction (RQ-PCR) in a cohort of 133 B-CLL patients and correlated the results with clinical outcome, and other known prognostic factors. LPL, ADAM29, LPL and ADAM29 ratios, as well as CD38 and ZAP-70 protein expression determined by multiparameter flow cytometry, were predictive of treatment-free survival. Multivariate Cox regression analysis identified LPL, ADAM29 and CD38 as independent prognostic markers. Evaluation of several disease characteristics in association with the LPL expression status of the patients' B-CLL cells showed highly significant differences for CD38 and ZAP-70 expression, suggesting a correlation of LPL expression with these established adverse prognostic factors. Sequential RQ-PCR analyses in a subset of 22 patients revealed that LPL mRNA expression was relatively stable in the majority of patients, whereas ADAM29 expression levels varied substantially over time. Furthermore, in a subgroup analysis, LPL provided prognostic information in both early stage (Binet A) and patients with more advanced disease (Binet B and C). Conversely, high ADAM29 expression was predictive of a long treatment-free interval in Binet stage A but did not retain its prognostic significance in Binet B and C patients. The LPL/ADAM29 expression ratio was not found to be an independent prognostic factor and did not offer any advantages over the use of LPL alone. Collectively, our data confirm a role for LPL as a novel prognostic indicator in B-CLL.
引用
收藏
页码:1053 / 1061
页数:9
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