N-cadherin in cancer metastasis, its emerging role in haematological malignancies and potential as a therapeutic target in cancer

被引:276
作者
Mrozik, Krzysztof Marek [1 ,2 ]
Blaschuk, Orest William [3 ]
Cheong, Chee Man [1 ,2 ]
Zannettino, Andrew Christopher William [1 ,2 ,4 ]
Vandyke, Kate [1 ,2 ]
机构
[1] Univ Adelaide, Fac Hlth & Med Sci, Adelaide Med Sch, Myeloma Res Lab, Adelaide, SA, Australia
[2] South Australian Hlth & Med Res Inst, Canc Theme, Adelaide, SA, Australia
[3] McGill Univ, Dept Surg, Div Urol, Montreal, PQ, Canada
[4] Univ South Australia, Ctr Canc Biol, Adelaide, SA, Australia
关键词
N-cadherin; Cancer; Metastasis; Haematological malignancies; Therapeutic target; EPITHELIAL-MESENCHYMAL TRANSITION; ACUTE MYELOID-LEUKEMIA; GROWTH-FACTOR RECEPTOR; CELL-CELL-ADHESION; TYROSINE KINASE INHIBITORS; HEMATOPOIETIC STEM-CELLS; INVASIVE BREAST-CANCER; BONE-MARROW NICHE; BETA-CATENIN; MULTIPLE-MYELOMA;
D O I
10.1186/s12885-018-4845-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
In many types of solid tumours, the aberrant expression of the cell adhesion molecule N-cadherin is a hallmark of epithelial-to-mesenchymal transition, resulting in the acquisition of an aggressive tumour phenotype. This transition endows tumour cells with the capacity to escape from the confines of the primary tumour and metastasise to secondary sites. In this review, we will discuss how N-cadherin actively promotes the metastatic behaviour of tumour cells, including its involvement in critical signalling pathways which mediate these events. In addition, we will explore the emerging role of N-cadherin in haematological malignancies, including bone marrow homing and microenvironmental protection to anti-cancer agents. Finally, we will discuss the evidence that N-cadherin may be a viable therapeutic target to inhibit cancer metastasis and increase tumour cell sensitivity to existing anti-cancer therapies.
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页数:16
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