共 121 条
Tropomyosin-related kinase B/brain derived-neurotrophic factor signaling pathway as a potential therapeutic target for colorectal cancer
被引:39
作者:
Akil, Hussein
[1
]
Perraud, Aurelie
[1
,2
]
Jauberteau, Marie-Odile
[1
,3
]
Mathonnet, Muriel
[1
,2
]
机构:
[1] Univ Limoges, Fac Med & Pharm, Federat Rech GEIST, LHCP,EA3842, F-87025 Limoges, France
[2] CHU Limoges, Serv Chirurg Digest Gen & Endocrinienne, F-87042 Limoges, France
[3] CHU Limoges, Serv Immunol, F-87042 Limoges, France
关键词:
Colorectal cancer;
Tyrosine kinase receptor B;
Brain-derived neurotrophic factor;
Therapeutic targets;
Cell survival;
EPITHELIAL-MESENCHYMAL TRANSITION;
HUMAN NEUROBLASTOMA-CELLS;
HUMAN TRKB GENE;
PHASE-I TRIAL;
TRUNCATED TRKB;
COLON-CANCER;
ANOIKIS RESISTANCE;
MULTIPLE-MYELOMA;
CEP-751;
KT-6587;
RECEPTOR TRKB;
D O I:
10.3748/wjg.v22.i2.490
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
100201 [内科学];
摘要:
Colorectal cancer (CRC) is the second most common cause of cancer-related death in western countries. Approximately one-quarter of newly diagnosed patients for CRC have metastases, and a further 40%-50% experience disease recurrence or develop metastases after all standard therapies. Therefore, understanding the molecular mechanisms involved in the progression of CRC and subsequently developing novel therapeutic targets is crucial to improve management of CRC and patients' long-term survival. Several tyrosine kinase receptors have been implicated in CRC development, progression and metastasis, including epidermal growth factor receptor (EGFR) and vascular EGFR. Recently, tropomyosin-related kinase B (TrkB), a tyrosine kinase receptor, has been reported in CRC and found to clearly exert several biological and clinical features, such as tumor cell growth and survival in vitro and in vivo, metastasis formation and poor prognosis. Here we review the significance of TrkB and its ligand brain derived-neurotrophic factor in CRC. We focus on their expression in CRC tumor samples, and their functional roles in CRC cell lines and in in vivo models. Finally we discuss therapeutic approaches that can lead to the development of novel therapeutic agents for treating TrkB-expressing CRC tumors.
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页码:490 / 500
页数:11
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