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Cell death induced in a human glioblastoma cell line by p(65)+Be neutrons combined with cisplatin.

作者信息

Benzina Sami, Fischer Barbara, Miternique-Grosse Anne, Dufour Patrick, Denis Jean-Marc, Bergerat Jean-Pierre, Gueulette John, Bischoff Pierre

机构信息

Laboratoire de Cancérologie Expérimentale et de Radiobiologie, EA-3430, IRCAD, Hôpitaux Universitaires, 1 place de l'Hôpital, F-67091 Strasbourg, France.

出版信息

Life Sci. 2006 Jul 4;79(6):513-8. doi: 10.1016/j.lfs.2006.01.037. Epub 2006 Mar 3.

DOI:10.1016/j.lfs.2006.01.037
PMID:16516239
Abstract

High linear energy transfer (LET) radiation have the ability to kill cancer cells resistant to conventional radiotherapy. On the other hand, protocols combining radiotherapy and chemotherapy are effective in eradicating certain inoperable cancers. In this study, we investigated the cytotoxicity of a co-treatment with fast neutrons and cisplatin in a human glioblastoma cell line, U-87. Cells cultured in vitro were irradiated with p(65)+Be neutrons in the presence of cisplatin. Cell survival and the induction of apoptosis and premature senescence were assessed at different time intervals thereafter, using a variety of methods. A marked reinforcement of the cytotoxicity was obtained when irradiation and cisplatin were associated. This reflected both an amplification of the apoptotic process and the induction of premature cell senescence. The efficiency of a combination between fast neutrons and cisplatin in inducing cell death in U-87 is more than additive. The present data concur with those we previously reported in a mouse lymphoma and suggest the potential utility of platinum compounds as adjuncts to future cancer therapy protocols using high-LET radiation.

摘要

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