Preliminary data suggestive of a novel translational approach to mesothelioma treatment: Imatinib mesylate with gemcitabine or pemetrexed

被引:43
作者
Bertino, Pietro
Porta, Camillo
Barbone, Dario
Germano, Serena
Busacca, Sara
Pinato, Sabrina
Tassi, Giancarlo
Favoni, Roberto
Gaudino, Giovanni [1 ]
Mutti, Luciano
机构
[1] Univ Piemonte Orientale, DISCAFF Dept, I-28100 Novara, Italy
[2] Univ Piemonte Orientale, DFBC Ctr, I-28100 Novara, Italy
[3] San Matteo Univ Hosp, IRCCS, Pavia, Italy
[4] Brescia Hosp, Chest Med Unit, Brescia, Italy
[5] Natl Canc Inst, Genoa, Italy
[6] Local Hlth Unit, I-11 Piemonte, Italy
关键词
D O I
10.1136/thx.2006.069872
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Background: Malignant mesothelioma is a cancer which is refractory to current treatments. Imatinib mesylate is a selective inhibitor of tyrosine kinases such as bcr-abl, c-Kit, c-Fms and platelet derived growth factor receptor beta (PDGFRb). PDGFRb is often overexpressed in mesothelioma cells and is a therapeutic target for imatinib in some solid tumours. A study was undertaken to assess whether imatinib alone or combined with chemotherapeutic agents may be effective for treating mesothelioma. Methods: Cultures from mesothelioma MMP, REN and ISTMES2 cell lines were treated with imatinib alone or in combination with a chemotherapeutic agent. Results: Imatinib induced cytotoxicity and apoptosis selectively on PDGFRb positive mesothelioma cells via blockade of receptor phosphorylation and interference with the Akt pathway. Of the chemotherapeutic agents tested in combination with imatinib, a synergistic effect was obtained with gemcitabine and pemetrexed. Conclusions: This study provides a rationale for a novel translational approach to the treatment of mesothelioma which relies on enhancement of tumour chemosensitivity by inhibition of Akt.
引用
收藏
页码:690 / 695
页数:6
相关论文
共 44 条
[1]   An overview of targeted treatments in cancer [J].
Abou-Jawde, R ;
Choueiri, T ;
Alemany, C ;
Mekhail, T .
CLINICAL THERAPEUTICS, 2003, 25 (08) :2121-2137
[2]   Effect of imatinib mesylate on neuroblastoma tumorigenesis and vascular endothelial growth factor expression [J].
Beppu, K ;
Jaboine, J ;
Merchant, MS ;
Mackall, CL ;
Thiele, CJ .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (01) :46-55
[3]  
BUMOR KJ, 2004, ARCH PATHOL LAB MED, V128, P538
[4]   SV40-dependent AKT activity drives mesothelial cell transformation after asbestos exposure [J].
Cacciotti, P ;
Barbone, D ;
Porta, C ;
Altomare, DA ;
Testa, JR ;
Mutti, L ;
Gaudino, G .
CANCER RESEARCH, 2005, 65 (12) :5256-5262
[5]   The presence of simian-virus 40 sequences in mesothelioma and mesothelial cells is associated with high levels of vascular endothelial growth factor [J].
Cacciotti, P ;
Strizzi, L ;
Vianale, G ;
Iaccheri, L ;
Libener, R ;
Porta, C ;
Tognon, M ;
Gaudino, G ;
Mutti, L .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2002, 26 (02) :189-193
[6]   SV40 replication in human mesothelial cells induces HGF/Met receptor activation: A model for viral-related carcinogenesis of human malignant mesothelioma [J].
Cacciotti, P ;
Libener, R ;
Betta, P ;
Martini, F ;
Porta, C ;
Procopio, A ;
Strizzi, L ;
Penengo, L ;
Tognon, M ;
Mutti, L ;
Gaudino, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (21) :12032-12037
[7]   Induction of stem cell factor/c-Kit/Slug signal transduction in multidrug-resistant malignant mesothelioma cells [J].
Catalano, A ;
Rodilossi, S ;
Rippo, MR ;
Caprari, P ;
Procopio, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (45) :46706-46714
[8]   Activity of a specific inhibitor of the BCR-ABL tyrosine kinase in the blast crisis of chronic myeloid leukemia and acute lymphoblastic leukemia with the philadelphia chromosome. [J].
Druker, BJ ;
Sawyers, CL ;
Kantarjian, H ;
Resta, DJ ;
Reese, SF ;
Ford, JM ;
Capdeville, R ;
Talpaz, M .
NEW ENGLAND JOURNAL OF MEDICINE, 2001, 344 (14) :1038-1042
[9]   Role of epidermal growth factor receptor degradation in gemcitabine-mediated cytotoxicity [J].
Feng, F. Y. ;
Varambally, S. ;
Tomlins, S. A. ;
Chun, P. Y. ;
Lopez, C. A. ;
Li, X. ;
Davis, M. A. ;
Chinnaiyan, A. M. ;
Lawrence, T. S. ;
Nyati, M. K. .
ONCOGENE, 2007, 26 (23) :3431-3439
[10]  
GARLEPP MJ, 1995, EUR RESPIR J, V8, P643