Cutaneous T-cell lymphoma cells are sensitive to rapamycin

被引:21
作者
Kremer, Melanie [1 ]
Sliva, Katja [1 ]
Klemke, Claus-Detlev [2 ]
Schnierle, Barbara S. [1 ]
机构
[1] Paul Ehrlich Inst, D-63225 Langen, Germany
[2] Ruprecht Karl Univ Heidelberg, Univ Med Ctr Mannheim, Dept Dermatol Venereol & Allergol, Mannheim, Germany
关键词
CTCL; mTOR; rapamycin; ENDOTHELIAL GROWTH-FACTOR; MYCOSIS-FUNGOIDES; THERAPY; EXPRESSION; ESTABLISHMENT; LINES;
D O I
10.1111/j.1600-0625.2010.01102.x
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100227 [皮肤病学];
摘要
Cutaneous T-cell lymphomas (CTCL) are characterised by clonal expansion of helper T lymphocytes that infiltrate the skin. Only a small number of cell lines exist to study cellular pathways leading to T-cell transformation and to identify new targets for intervention. We wanted to investigate the inhibition of mTOR as a possible therapeutic target in CTCL. Primary cells of patients with Sezary syndrome (SS) and conventional CTCL cell lines were analysed. Constitutive activation of mTOR was found, and concomitantly, we could show that rapamycin, a specific inhibitor of mTOR, inhibits CTCL cell growth in vitro by induction of cell cycle arrest. Using a previously established animal model for CTCL, we additionally observed upon rapamycin treatment tumor growth inhibition in vivo. In summary, primary cells from patients with SS as well as CTCL cell lines allowed us to identify mTOR as an important target for intervention.
引用
收藏
页码:800 / 805
页数:6
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