Metastasis mechanisms

被引:584
作者
Geiger, Thomas R. [1 ]
Peeper, Daniel S. [1 ]
机构
[1] Netherlands Canc Inst, Div Mol Genet, NL-1066 CX Amsterdam, Netherlands
来源
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER | 2009年 / 1796卷 / 02期
关键词
Cancer; Metastasis; EMT; Anoikis; Stem cells; Microenvironment; EPITHELIAL-MESENCHYMAL TRANSITION; BREAST-CANCER METASTASIS; NEUROTROPHIC RECEPTOR TRKB; CUTANEOUS MALIGNANT-MELANOMA; GENE-EXPRESSION SIGNATURE; CIRCULATING TUMOR-CELLS; FOCAL-ADHESION KINASE; E-CADHERIN EXPRESSION; GROWTH FACTOR-C; NF-KAPPA-B;
D O I
10.1016/j.bbcan.2009.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Metastasis, the spread of malignant cells from a primary tumor to distant sites, poses the biggest problem to cancer treatment and is the main cause of death of cancer patients. It occurs in a series of discrete steps, which have been modeled into a "metastatic cascade". In this review, we comprehensively describe the molecular and cellular mechanisms underlying the different steps, including Epithelial-Mesenchymal Transition (EMT), invasion, anoikis, angiogenesis, transport through vessels and outgrowth of secondary tumors. Furthermore, we implement recent findings that have broadened and challenged the classical view on the metastatic cascade, for example the establishment of a "premetastatic niche", the requirement of stem cell-like properties, the role of the tumor stroma and paracrine interactions of the tumor with cells in distant anatomical sites. A better understanding of the molecular processes underlying metastasis will conceivably present us with novel targets for therapeutic intervention. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:293 / 308
页数:16
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