Acute Myeloid Leukemia Research - AML, Symptoms, Treatment, Information

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Downregulation of neuropilin-1 in patients with acute myeloid leukemia treated with thalidomide.

Kreuter M, Steins M, Woelke K, Buechner T, Berdel WE, Mesters RM

Department of Medicine/Hematology and Oncology, University of Muenster, Muenster, Germany.

OBJECTIVE: Neuropilin-1 (NRP-1), a non-tyrosine kinase receptor functioning as a mediator of angiogenesis and neuronal guidance, was recently found to be significantly overexpressed in newly diagnosed acute myeloid leukemia (AML) patients with significant correlation to survival. The role of NRP-1 in refractory or relapsed AML patients and its regulation during anti-angiogenic treatment remain to be elucidated. METHODS: Bone marrow biopsies of 10 patients with refractory or relapsed AML were evaluated for NRP-1 expression by immunohistochemical analysis, and NRP-1 expression level was determined before and after start of thalidomide therapy and correlated to response and growth factor expression. RESULTS: NRP-1 expression was significantly increased in AML patients [median 7 arbitrary units (AU)] when compared with controls (n = 38, median 2.75 AU). Under thalidomide treatment, a marked difference in the course of NRP-1 expression between responders and non-responders was observed, however, without a statistical significance (P = 0.071) being reached. Additionally, a significant correlation of the NRP-1 expression level to microvessel density could be detected under treatment with thalidomide (P = 0.018). CONCLUSION: Our data provide evidence of increased NRP-1 expression in relapsed or refractory AML. Additionally, our results suggest that thalidomide-induced antileukemic properties might at least in part be mediated by NRP-1 downregulation.

Published 10 October 2007 in Eur J Haematol, 79(5): 392-7.
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Acute Myeloid Leukemia Research Today Archive:

Volume 1 (2004)
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