Short telomeres and high telomerase activity in T-cell prolymphocytic leukemia

被引:23
作者
Roeth, A.
Duerig, J.
Himmelreich, H.
Bug, S.
Siebert, R.
Duehrsen, U.
Lansdorp, P. M.
Baerlocher, G. M.
机构
[1] Univ Duisburg Gesamthsch, Univ Hosp, Dept Hematol, Essen, Germany
[2] Univ Hosp, Dept Hematol, Bern, Switzerland
[3] Univ Hosp, Dept Clin Res, Bern, Switzerland
[4] Univ Kiel, Hosp Schleswig Holstein, Inst Human Genet, Kiel, Germany
[5] BC Canc Res Ctr, Terry Fox Lab, Vancouver, BC, Canada
[6] Univ British Columbia, Dept Med, Vancouver, BC, Canada
关键词
T-cell leukemia; telomere length; telomerase; telomerase inhibitor;
D O I
10.1038/sj.leu.2404968
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
To test the role of telomere biology in T-cell prolymphocytic leukemia (T-PLL), a rare aggressive disease characterized by the expansion of a T-cell clone derived from immuno-competent post-thymic T-lymphocytes, we analyzed telomere length and telomerase activity in subsets of peripheral blood leukocytes from 11 newly diagnosed or relapsed patients with sporadic T-PLL. Telomere length values of the leukemic T cells (mean +/- s.d.: 1.53 +/- 0.65 kb) were all below the 1st percentile of telomere length values observed in T cells from healthy age-matched controls whereas telomere length of normal T- and B cells fell between the 1st and 99th percentile of the normal distribution. Leukemic T cells exhibited high levels of telomerase and were sensitive to the telomerase inhibitor BIBR1532 at doses that showed no effect on normal, unstimulated T cells. Targeting the short telomeres and telomerase activity in T-PLL seems an attractive strategy for the future treatment of this devastating disease.
引用
收藏
页码:2456 / 2462
页数:7
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