Antitumor activities of the targeted multi-tyrosine kinase inhibitor lenvatinib (E7080) against RET gene fusion-driven tumor models

被引:243
|
作者
Okamoto, Kiyoshi [1 ]
Kodama, Kotaro [1 ]
Takase, Kazuma [1 ]
Sugi, Naoko Hata [1 ]
Yamamoto, Yuji [1 ]
Iwata, Masao [1 ]
Tsuruoka, Akihiko [1 ]
机构
[1] Eisai & Co Ltd, Tsukuba, Ibaraki 3002635, Japan
关键词
Lenvatinib; RET inhibitor; Anti-cancer drug; Xenograft model; Lung cancer; Thyroid cancer; PAPILLARY THYROID-CARCINOMA; LUNG ADENOCARCINOMA; CELL-LINE; CANCER; ALK; IDENTIFICATION; SENSITIVITY; LEUKEMIA;
D O I
10.1016/j.canlet.2013.07.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
RET gene fusions are recurrent oncogenes identified in thyroid and lung carcinomas. Lenvatinib is a multi-tyrosine kinase inhibitor currently under evaluation in several clinical trials. Here we evaluated lenvatinib in RET gene fusion-driven preclinical models. In cellular assays, lenvatinib inhibited autophosphorylation of KIF5B-RET. CCDC6-RET, and NcoA4-RET. Lenvatinib suppressed the growth of CCDC6-RET human thyroid and lung cancer cell lines, and as well, suppressed anchorage-independent growth and tumorigenicity of RET gene fusion-transformed NIH3T3 cells. These results demonstrate that lenvatinib can exert antitumor activity against RET gene fusion-driven tumor models by inhibiting oncogenic RET gene fusion signaling. (C) 2013 The Authors. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:97 / 103
页数:7
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