The role of the tissue microenvironment in the regulation of cancer cell motility and invasion

被引:144
作者
Brabek, Jan [1 ]
Mierke, Claudia T. [2 ]
Roesel, Daniel [1 ]
Vesely, Pavel [3 ]
Fabry, Ben [2 ]
机构
[1] Charles Univ Prague, Fac Sci, Dept Cell Biol, Prague, Czech Republic
[2] Univ Erlangen Nurnberg, Dept Phys, Biophys Grp, D-8520 Erlangen, Germany
[3] AS CR, Inst Mol Genet, Prague, Czech Republic
关键词
EXTRACELLULAR-MATRIX; TRANSENDOTHELIAL MIGRATION; ENDOTHELIAL-CELLS; AMEBOID MOVEMENT; CARCINOMA-CELLS; TUMOR-CELLS; E-SELECTIN; METASTASIS; ADHESION; TRANSMIGRATION;
D O I
10.1186/1478-811X-8-22
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
During malignant neoplastic progression the cells undergo genetic and epigenetic cancer-specific alterations that finally lead to a loss of tissue homeostasis and restructuring of the microenvironment. The invasion of cancer cells through connective tissue is a crucial prerequisite for metastasis formation. Although cell invasion is foremost a mechanical process, cancer research has focused largely on gene regulation and signaling that underlie uncontrolled cell growth. More recently, the genes and signals involved in the invasion and transendothelial migration of cancer cells, such as the role of adhesion molecules and matrix degrading enzymes, have become the focus of research. In this review we discuss how the structural and biomechanical properties of extracellular matrix and surrounding cells such as endothelial cells influence cancer cell motility and invasion. We conclude that the microenvironment is a critical determinant of the migration strategy and the efficiency of cancer cell invasion.
引用
收藏
页数:8
相关论文
共 75 条
[1]
ABERCROMBIE M, 1978, MED BIOL, V56, P299
[2]
Intravascular origin of metastasis from the proliferation of endothelium-attached tumor cells: a new model for metastasis [J].
Al-Mehdi, AB ;
Tozawa, K ;
Fisher, AB ;
Shientag, L ;
Lee, A ;
Muschel, RJ .
NATURE MEDICINE, 2000, 6 (01) :100-102
[3]
Localization of matrix metalloproteinase MMP-2 to the surface of invasive cells by interaction with integrin alpha v beta 3 [J].
Brooks, PC ;
Stromblad, S ;
Sanders, LC ;
vonSchalscha, TL ;
Aimes, RT ;
StetlerStevenson, WG ;
Quigley, JP ;
Cheresh, DA .
CELL, 1996, 85 (05) :683-693
[4]
Calpain 2 and Src dependence distinguishes mesenchymal and amoeboid modes of tumour cell invasion: a link to integrin function [J].
Carragher, N. O. ;
Walker, S. M. ;
Carragher, L. A. Scott ;
Harris, F. ;
Sawyer, T. K. ;
Brunton, V. G. ;
Ozanne, B. W. ;
Frame, M. C. .
ONCOGENE, 2006, 25 (42) :5726-5740
[5]
INCREASED PLASMA-LEVELS OF LEUKOTRIENES IN RESPONSE TO NEUROTENSIN [J].
CARRAWAY, RE ;
COCHRANE, DE ;
SALMONSEN, R .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES-SERIES, 1992, 668 :317-319
[6]
Tumor necrosis factor α (TNF-α) receptor-II is required for TNF-α-induced leukocyte-endothelial interaction in vivo [J].
Chandrasekharan, Unni M. ;
Siemionow, Maria ;
Unsal, Murat ;
Yang, Lin ;
Poptic, Earl ;
Bohn, Justin ;
Ozer, Kagan ;
Zhou, Zhongmin ;
Howe, Philip H. ;
Penn, Marc ;
DiCorleto, Paul E. .
BLOOD, 2007, 109 (05) :1938-1944
[7]
Nuclear shape, mechanics, and mechanotransduction [J].
Dahl, Kris Noel ;
Ribeiro, Alexandre J. S. ;
Lammerding, Jan .
CIRCULATION RESEARCH, 2008, 102 (11) :1307-1318
[8]
One-dimensional topography underlies three-dimensional fibrillar cell migration [J].
Doyle, Andrew D. ;
Wang, Francis W. ;
Matsumoto, Kazue ;
Yamada, Kenneth M. .
JOURNAL OF CELL BIOLOGY, 2009, 184 (04) :481-490
[9]
BIOLOGICAL DIVERSITY IN METASTATIC NEOPLASMS - ORIGINS AND IMPLICATIONS [J].
FIDLER, IJ ;
HART, IR .
SCIENCE, 1982, 217 (4564) :998-1003
[10]
FRIEDL P, 1994, IMMUNOLOGY, V82, P617