Hypoxia-Mediated Metastasis

被引:55
作者
Chang, Joan [1 ]
Erler, Janine [1 ]
机构
[1] Univ Copenhagen, BRIC, DK-2200 Copenhagen N, Denmark
来源
TUMOR MICROENVIRONMENT AND CELLULAR STRESS: SIGNALING, METABOLISM, IMAGING, AND THERAPEUTIC TARGETS | 2014年 / 772卷
关键词
Hypoxia; Metastasis; Extracellular matrix (ECM); Epithelial-mesenchymal transition (EMT); Microenvironment; Angiogenesis; EPITHELIAL-MESENCHYMAL TRANSITION; CIRCULATING TUMOR-CELLS; ENDOTHELIAL PROGENITOR CELLS; GREEN FLUORESCENT PROTEIN; CHEMOKINE RECEPTOR CXCR4; INDUCIBLE FACTOR 1-ALPHA; BREAST-CANCER CELLS; LYSYL OXIDASE; IN-VIVO; ANGIOGENIC SWITCH;
D O I
10.1007/978-1-4614-5915-6_3
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Metastasis is responsible for more than 90 % of deaths among cancer patient. It is a highly complex process that involves the interplay between cancer cells, the tumor microenvironment, and even noncancerous host cells. Metastasis can be seen as a step-wise process: acquisition of malignant phenotype, invasion into surrounding tissue, intravasation into blood vessels, survival in circulation, extravasation to distant sites, and colonization of new organs. Before the actual metastatic process, the secondary site is also prepared for the arrival of the cancer cells through formation of "premetastatic niches." Hypoxia (low oxygen tension) is commonly found in solid tumors more than a few millimeters cubed and often is associated with a poor prognosis. Hypoxia increases angiogenesis, cancer cell survival, and metastasis. This chapter described how hypoxia regulates each step of the metastatic process and how blocking hypoxia-driven metastasis through targeting hypoxia-inducible factor 1, or downstream effector molecules such as the lysyl oxidase family may represent highly effective preventive strategies against metastasis in cancer patients.
引用
收藏
页码:55 / 81
页数:27
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