Preclinical intravital microscopy of the tumour-stroma interface: invasion, metastasis, and therapy response

被引:123
作者
Alexander, Stephanie [1 ]
Weigelin, Bettina [2 ]
Winkler, Frank [3 ,4 ,5 ]
Friedl, Peter [1 ,2 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Dept Genitourinary Med Oncol, David H Koch Ctr Appl Res Genitourinary Canc, Houston, TX 77030 USA
[2] Radboud Univ Nijmegen, Med Ctr, Dept Cell Biol, NL-6525 ED Nijmegen, Netherlands
[3] Heidelberg Univ, Neurol Clin, Dept Neurooncol, Heidelberg, Germany
[4] Heidelberg Univ, Natl Ctr Tumor Dis, Heidelberg, Germany
[5] German Canc Res Ctr, Heidelberg, Germany
关键词
GREEN FLUORESCENT PROTEIN; IN-VIVO; REAL-TIME; T-CELLS; MULTIPHOTON MICROSCOPY; CANCER-CELL; MIGRATION; REVEALS; MOUSE; MICROENVIRONMENT;
D O I
10.1016/j.ceb.2013.07.001
中图分类号
Q2 [细胞生物学];
学科分类号
071013 [干细胞生物学];
摘要
Key steps of cancer progression and therapy response depend upon interactions between cancer cells with the reactive tumour microenvironment. Intravital microscopy enables multimodal and multi-scale monitoring of cancer progression as a dynamic step-wise process within anatomic and functional niches provided by the microenvironment. These niches deliver cell-derived and matrix-derived signals that enable cell subsets or single cancer cells to survive, migrate, grow, undergo dormancy, and escape immune surveillance. Beyond basic research, intravital microscopy has reached preclinical application to identify mechanisms of tumour-stroma interactions and outcome. We here summarise how n-dimensional 'dynamic histopathology' of tumours by intravital microscopy shapes mechanistic insight into cell-cell and cell-tissue interactions that underlie single-cell and collective cancer invasion, metastatic seeding at distant sites, immune evasion, and therapy responses.
引用
收藏
页码:659 / 671
页数:13
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