Comparison of in vitro and in vivo approaches to studying brain colonization by breast cancer cells

被引:19
作者
Lorger, M. [1 ]
Lee, H. [1 ]
Forsyth, J. S. [1 ]
Felding-Habermann, B. [1 ]
机构
[1] Scripps Res Inst, San Diego, CA 92037 USA
关键词
Brain metastasis; Breast cancer; In vitro; In vivo; Blood brain barrier; Transendothelial migration; Extravasation; Brain metastasis model; CAPILLARY ENDOTHELIAL-CELLS; METASTASIS; BARRIER; MODEL; PERMEABILITY; MANAGEMENT; INVASION;
D O I
10.1007/s11060-011-0550-4
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Brain metastases occur in 20 to 40% of patients with metastatic breast cancer. The process is complex and depends on successful cancer cell evasion from the primary tumor, distribution and survival within the blood stream and cerebral microvasculature, penetration of the blood brain barrier and proliferation within the brain microenvironment. The initial steps of brain colonization are difficult to study in vivo. Therefore, in vitro assays have been developed to mimic this process. Most commonly, in vitro studies of brain colonization focus on tumor cell adhesion to brain endothelial cells and transendothelial migration. We previously investigated breast cancer brain colonization from the blood stream in vivo and defined the time and process of brain entry for five different cancer cell lines in a mouse model. We now investigated if in vitro approaches can reliably emulate the initial steps that determine successful brain colonization in vivo. To this end, we optimized an in vitro model of the vascular blood brain barrier and compared the brain invasion properties of the in vivo characterized cell models with their ability to interact with and penetrate the blood brain barrier model in vitro. Our results show that the in vitro findings correlate only poorly with the vivo results. The limitations of the in vitro approaches are discussed in light of the in vivo processes. We conclude that investigation of mechanisms supporting the earliest steps of breast cancer brain metastasis from the blood stream will depend on in vivo analyses.
引用
收藏
页码:689 / 696
页数:8
相关论文
共 34 条
[1]   Management of brain metastases: the indispensable role of surgery [J].
Al-Shamy, George ;
Sawaya, Raymond .
JOURNAL OF NEURO-ONCOLOGY, 2009, 92 (03) :275-282
[2]   EXPERIMENTAL-MODEL FOR CEREBRAL METASTASIS - PRELIMINARY LIGHT AND ULTRASTRUCTURAL STUDIES [J].
BALLINGER, WE ;
SCHIMPFF, RD .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1979, 38 (01) :19-34
[3]   What is the blood-brain barrier (not)? [J].
Bechmann, Ingo ;
Galea, Ian ;
Perry, V. Hugh .
TRENDS IN IMMUNOLOGY, 2007, 28 (01) :5-11
[4]   Microregional extracellular matrix heterogeneity in brain modulates glioma cell invasion [J].
Bellail, AC ;
Hunter, SB ;
Brat, DJ ;
Tan, C ;
Van Meir, EG .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2004, 36 (06) :1046-1069
[5]   Matrix metalloproteinase-9 triggers the angiogenic switch during carcinogenesis [J].
Bergers, G ;
Brekken, R ;
McMahon, G ;
Vu, TH ;
Itoh, T ;
Tamaki, K ;
Tanzawa, K ;
Thorpe, P ;
Itohara, S ;
Werb, Z ;
Hanahan, D .
NATURE CELL BIOLOGY, 2000, 2 (10) :737-744
[6]   Genes that mediate breast cancer metastasis to the brain [J].
Bos, Paula D. ;
Zhang, Xiang H. -F. ;
Nadal, Cristina ;
Shu, Weiping ;
Gomis, Roger R. ;
Nguyen, Don X. ;
Minn, Andy J. ;
van de Vijver, Marc J. ;
Gerald, William L. ;
Foekens, John A. ;
Massague, Joan .
NATURE, 2009, 459 (7249) :1005-U137
[7]   The Vascular Basement Membrane as "Soil'' in Brain Metastasis [J].
Carbonell, W. Shawn ;
Ansorge, Olaf ;
Sibson, Nicola ;
Muschel, Ruth .
PLOS ONE, 2009, 4 (06)
[8]  
DeAngelis LM, 2008, J SUPPORT ONCOL, V6, P87
[9]   Permeability studies on in vitro blood-brain barrier models: Physiology, pathology, and pharmacology [J].
Deli, MA ;
Abraham, CS ;
Kataoka, Y ;
Niwa, M .
CELLULAR AND MOLECULAR NEUROBIOLOGY, 2005, 25 (01) :59-127
[10]   CHARACTERIZATION OF THE HUMAN FACTOR-VIII PROCOAGULANT PROTEIN WITH A HETEROLOGOUS PRECIPITATING ANTIBODY [J].
FULCHER, CA ;
ZIMMERMAN, TS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1982, 79 (05) :1648-1652