Protein tyrosine kinase inhibitors in cancer therapy

被引:5
|
作者
Boutayeb, S. [1 ]
Zakkouri, F. Z. [1 ]
Aitelhaj, M. [1 ]
Mesmoudi, M. [1 ]
Boutayeb, A. [2 ]
Boutayeb, W. [2 ]
Mrabti, H. [1 ]
Errihani, H. [1 ]
机构
[1] CHU Ibn Slum, Inst Natl Oncol, Serv Oncol Med, Rabat, Morocco
[2] Univ Mohammed 1, Fac Sci, Unite Biostat, Oujda, Morocco
来源
PATHOLOGIE BIOLOGIE | 2012年 / 60卷 / 04期
关键词
Tyrosine kinase inhibitor; Cancer; Signal transduction; CELL LUNG-CANCER; PHASE-III; IMATINIB MESYLATE; DOUBLE-BLIND; VANDETANIB; SUNITINIB; ERLOTINIB; 1ST-LINE;
D O I
10.1016/j.patbio.2012.05.007
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
The tyrosine kinase inhibitors (TKI) are small molecules of low molecular weight that inhibit tyrosine kinases, enzymes responsible for the activation of signal transduction cascades. Currently, a number of TKI received approval in various cancers, while others are in clinical development process: TKI are specifically clinically active when they target a tyrosine kinase (TK) with constitutional activity subsequent to a mutation, being then a master-gene driving transformation and tumour progression. Already, this drug-family provides a major therapeutic weapon against cancer. (C) 2012 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:229 / 233
页数:5
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