| Literature DB >> 17898784 |
A Röth1, J Dürig, H Himmelreich, S Bug, R Siebert, U Dührsen, P M Lansdorp, G M Baerlocher.
Abstract
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.Entities:
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Year: 2007 PMID: 17898784 DOI: 10.1038/sj.leu.2404968
Source DB: PubMed Journal: Leukemia ISSN: 0887-6924 Impact factor: 11.528