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Cancer Invasion and the Microenvironment: Plasticity and Reciprocity
被引:1521
|作者:
Friedl, Peter
[1
,2
,3
,4
]
Alexander, Stephanie
[2
,3
,4
]
机构:
[1] Radboud Univ Nijmegen, Med Ctr, Dept Cell Biol, NL-6500 HC Nijmegen, Netherlands
[2] Univ Texas MD Anderson Canc Ctr, David H Koch Ctr Appl Res Genitourinary Canc, Dept Genitourinary Med Oncol, Houston, TX 77030 USA
[3] Univ Wurzburg, Dept Dermatol, D-97080 Wurzburg, Germany
[4] Univ Wurzburg, Rudolf Virchow Ctr, DFG Res Ctr Expt Biomed, D-97080 Wurzburg, Germany
来源:
关键词:
EPITHELIAL-MESENCHYMAL TRANSITION;
COLLECTIVE CELL-MIGRATION;
CIRCULATING TUMOR-CELLS;
E-CADHERIN;
EXTRACELLULAR-MATRIX;
TGF-BETA;
LEUKOCYTE MIGRATION;
ADHERENS JUNCTIONS;
CARCINOMA-CELLS;
DRIVES INVASION;
D O I:
10.1016/j.cell.2011.11.016
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Cancer invasion is a cell- and tissue-driven process for which the physical, cellular, and molecular determinants adapt and react throughout the progression of the disease. Cancer invasion is initiated and maintained by signaling pathways that control cytoskeletal dynamics in tumor cells and the turnover of cell-matrix and cell-cell junctions, followed by cell migration into the adjacent tissue. Here, we describe the cell-matrix and cell-cell adhesion, protease, and cytokine systems that underlie tissue invasion by cancer cells. We explain how the reciprocal reprogramming of both the tumor cells and the surrounding tissue structures not only guides invasion, but also generates diverse modes of dissemination. The resulting "plasticity" contributes to the generation of diverse cancer invasion routes and programs, enhanced tumor heterogeneity, and ultimately sustained metastatic dissemination.
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页码:992 / 1009
页数:18
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