Role and targeting of anaplastic lymphoma kinase in cancer

被引:104
作者
Della Corte, Carminia Maria [1 ]
Viscardi, Giuseppe [1 ]
Di Liello, Raimondo [1 ]
Fasano, Morena [1 ]
Martinelli, Erika [1 ]
Troiani, Teresa [1 ]
Ciardiello, Fortunato [1 ]
Morgillo, Floriana [1 ]
机构
[1] Univ Campania Luigi Vanvitelli, Dept Expt & Internal Med F Magrassi, Med Oncol, Via S Pansini 5, I-80131 Naples, Italy
关键词
ALK; Crizotinib; Alectinib; Ceritinib; Tyrosine kinase inhibitor; Resistance; CELL LUNG-CANCER; RECEPTOR TYROSINE KINASE; ALK INHIBITOR ALECTINIB; NON-HODGKINS-LYMPHOMA; CRIZOTINIB RESISTANCE; OPEN-LABEL; ANTITUMOR-ACTIVITY; SINGLE-ARM; MUTATIONS; REARRANGEMENT;
D O I
10.1186/s12943-018-0776-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Anaplastic lymphoma kinase (ALK) gene activation is involved in the carcinogenesis process of several human cancers such as anaplastic large cell lymphoma, lung cancer, inflammatory myofibroblastic tumors and neuroblastoma, as a consequence of fusion with other oncogenes (NPM, EML4, TIM, etc) or gene amplification, mutation or protein overexpression. ALK is a transmembrane tyrosine kinase receptor that, upon ligand binding to its extracellular domain, undergoes dimerization and subsequent autophosphorylation of the intracellular kinase domain. When activated in cancer it represents a target for specific inhibitors, such as crizotinib, ceritinib, alectinib etc. which use has demonstrated significant effectiveness in ALK-positive patients, in particular ALK-positive non-small cell lung cancer. Several mechanisms of resistance to these inhibitors have been described and new strategies are underway to overcome the limitations of current ALK inhibitors.
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页数:9
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