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Spindle Assembly Checkpoint as a Potential Target in Colorectal Cancer: Current Status and Future Perspectives
被引:14
|作者:
Diogo, Vania
[1
,2
]
Teixeira, Joana
[1
,2
]
Silva, Patricia M. A.
[1
,2
,3
]
Bousbaa, Hassan
[1
,4
]
机构:
[1] CESPU, Inst Invest & Formacao Avancada Ciencias & Tecnol, Inst Univ Ciencias Saude, Gandra, Paredes, Portugal
[2] Univ Algarve, Dept Ciencias Biomed & Med, Faro, Portugal
[3] Univ Algarve, Ctr Biomed Res CBMR, Faro, Portugal
[4] Univ Porto, Ctr Interdisciplinar Invest Marinha & Ambiental C, Oporto, Portugal
关键词:
Aneuploidy;
Cancer;
Gene expression;
Spindle checkpoint genes;
Targeted therapy;
AURORA KINASE INHIBITOR;
SMALL-MOLECULE INHIBITOR;
POLO-LIKE KINASES;
MITOTIC CHECKPOINT;
CHROMOSOMAL INSTABILITY;
ANTITUMOR-ACTIVITY;
COLON-CANCER;
PHASE-I;
SELECTIVE INHIBITOR;
EXPRESSION PROFILES;
D O I:
10.1016/j.clcc.2016.06.006
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
Colorectal cancer (CRC), one of the most common malignancies worldwide, is often diagnosed at an advanced stage, and resistance to chemotherapeutic and existing targeted therapy is a major obstacle to its successful treatment. New targets that offer alternative clinical options are therefore urgently needed. Recently, perturbation of the spindle assembly checkpoint (SAC), the surveillance mechanism that maintains anaphase inhibition until all chromosomes reach the metaphase plate, has been regarded as a promising target to fight cancer cells, either alone or in combination regimens. Consistent with this strategy, many cancers, including CRC, exhibit altered expression of SAC genes. In this article, we review our current knowledge on SAC activity status in CRC, and on current anti-CRC strategies and future therapeutic perspectives on the basis of SAC targeting experiments in vitro and in animal models. (C) 2016 Elsevier Inc. All rights reserved.
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页码:1 / 8
页数:8
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