Molecular networks that regulate cancer metastasis

被引:312
作者
Spano, Daniela [1 ,2 ]
Heck, Chantal [3 ]
De Antonellis, Pasqualino [1 ,2 ]
Christofori, Gerhard [3 ]
Zollo, Massimo [1 ,2 ]
机构
[1] CEINGE, Naples, Italy
[2] Univ Naples Federico II, Dept Biochem & Med Biotechnol DBBM, Naples, Italy
[3] Univ Basel, Inst Biochem & Genet, Dept Biomed, Basel, Switzerland
关键词
Invasion; Amoeboid; Mesenchymal; Lymphogenic; Intravasation; Extravasation; Microenvironment; Metastatic outgrowth; LYMPH-NODE METASTASIS; EPITHELIAL-MESENCHYMAL TRANSITION; CHEMOKINE RECEPTOR CCR7; SQUAMOUS-CELL CARCINOMA; GROWTH-FACTOR-C; LUNG METASTASIS; UP-REGULATION; TUMOR-CELLS; SUPPRESSOR-CELLS; IN-VIVO;
D O I
10.1016/j.semcancer.2012.03.006
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Tumor metastases are responsible for approximately 90% of all cancer-related deaths. Although many patients can be cured, in the US and UK, cancer still causes 730,000 deaths every year, and it is second only to cardiovascular disease as a cause of death. The functional roles of many critical players involved in metastasis have been delineated in great detail in recent years, due to the draft of the human genome and to many associated discoveries. Here, we address several genetic events and critical factors that define the metastatic phenotype acquired during tumorigenesis. This involves molecular networks that promote local cancer-cell invasion, single-cell invasion, formation of the metastatic microenvironment of primary tumors, intravasation, lymphogenic metastasis, extravasation, and metastatic outgrowth. Altogether, these functional networks of molecules contribute to the development of a selective environment that promotes the seeding and malignant progression of tumorigenic cells in distant organs. We include here candidate target proteins and signaling pathways that are now under clinical investigation. Although many of these trials are still ongoing, they provide the basis for the development of new aspects in the treatment of metastatic cancers, which involves inhibition of these proteins and their molecular networks. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:234 / 249
页数:16
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