Role of the Endothelium during Tumor Cell Metastasis: Is the Endothelium a Barrier or a Promoter for Cell Invasion and Metastasis?

Mierke, Claudia Tanja

doi:https://doi.org/10.1155/2008/183516

Journal of Biophysics

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Review Article | Open Access

Volume 2008 | Article ID 183516 | https://doi.org/10.1155/2008/183516

Role of the Endothelium during Tumor Cell Metastasis: Is the Endothelium a Barrier or a Promoter for Cell Invasion and Metastasis?

Claudia Tanja Mierke¹

Academic Editor: Miklós S. Z. Kellermayer

Received09 May 2008

Revised12 Oct 2008

Accepted11 Dec 2008

Published05 Mar 2009

Abstract

The malignancy of cancer disease depends on the ability of the primary tumor to metastasize to distant organs. The process of the metastasis formation has largely been analyzed, but still main pathways regarding the extravasation step at the end of the metastasis formation process are controversially discussed. An agreement has been reached about the importance of the endothelium to promote metastasis formation either by enhancing the growth of the primary tumor or by homing (targeting) the tumor cells to blood or lymph vessels. The mechanical properties of the invading tumor cells become the focus of several studies, but the endothelial cell mechanical properties are still elusive. This paper describes the different roles of the endothelium in the process of metastasis formation and focuses on a novel role of the endothelium in promoting tumor cell invasion. It discusses how novel biophysical tools and in vivo animal models help to determine the role of the endothelium in the process of tumor cell invasion. Evidence is provided that cell mechanical properties, for example, contractile force generation of tumor cells, are involved in the process of tumor cell invasion.

1. Introduction

The coordinated regulation of cell adhesion and cell motility especially the migration of cells in a three-dimensional (3D) environment (cell invasion) is essential for the development and function of almost all multicellular organisms. The transformation of cell-cell and cell-matrix adhesions as well as the loss of contact responsiveness is an indicator for the malignancy of tumors [1, 2]. Cell invasion is a driving force in malignant tumor diseases, for example, in the progression of primary tumor outgrowth and in the process of metastasis formation. The malignancy of neoplasms is determined by the capability of single tumor cells to invade into the surrounding tissue, intravasate into blood or lymph vessels, be transported, possibly extravasate and invade into the connective tissue, proliferate, and finally metastasize [3, 4] (Figure 1).

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Cell invasion is a central step in the process of metastasis formation. The prerequisites for cell invasion involved in the metastasis formation process are (1) cell adhesion (adhesion strength), (2) force generation, (3) detachment (deadhesion and cytoskeletal remodeling), and (4) matrix composition and remodeling via enzymes (Figure 2). The balance of all these parameters determines the cell invasiveness, for example, the migration speed in a 3D extracellular matrix. All these considerations might play a more or less important role in cell invasion depending on the cell type and tissue origin, gene, or protein expression pattern of a cell, the environment (growth factors, matrix constituents, and mechanical stiffness), and adjacent cells. In line with cell invasion, the interaction of a cell with the neighboring cells underlies also mechanical properties of the cytoskeleton of the two adjacent cells.

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Figure 2

Prerequisites for tumor cell migration on a 2D substrate and tumor cell invasion in a 3D extracellular matrix. (a) Scanning electron microscopic image of an MDA-MB-231 breast carcinoma cell on a planar glass and (b) transmission electron microscopic image of an MDA-MB-231 cell invaded in 3D collagen gel matrix. (a) For proper 2D motility, a cell needs to adhere/deadhere fast, remodel its cytoskeleton fast, and possess a high CSK-fluidity. (d) For proper 3D motility, a cell needs, in addition to the 2D motility properties, to generate high contractile forces, and the cells needs to overcome the viscous drag of the surrounding extracellular matrix to move forward.

Alterations of cell-cell and cell-matrix interactions are mirrored in the cytoskeleton and account for the ability of tumor cells to cross tissue boundaries and to disseminate to distant organ sites. Many adhesion molecules implicated in tumor metastasis have been identified, but there exist only a few studies with a broad designed approach. Several adhesion or cell surface receptors have been identified to act either as negative, for example, E-Cadherin [5] or positive factors, for example, αvβ3, CD24, and CXCR2 of tumor invasion and metastasis formation [6–8]. The focus of this paper is on the processes of cell invasion and transendothelial migration of tumor cells as well as on their prerequisites including the presentation of novel biophysical tools and in vivo metastasis models. The emphasis is on the function of the endothelium in the process of metastasis formation, such that it promotes tumor cell invasion.

2. Tumor Cell Invasion

2.1. How Do Cell-Matrix Adhesion Receptors Influence Tumor Cell Invasion?

To generate tractions especially in a 3D extracellular matrix, the cells need to have a tight connection between the extracellular matrix and the intracellular cytoskeleton via focal adhesions and cell-matrix receptors. This connection is commonly facilitated by transmembrane proteins like integrin cell adhesion receptors. Integrins are heterodimeric proteins that are involved in cell adhesion, migration, and invasion processes and regulate the cell cycle. The protein family of human integrins comprises 18 α- and 8 β-subunits [9]. At least 24 different α-β-heterodimer combinations have been identified, that are capable of binding to a large variety of ligands, among them were components of the extracellular matrix (e.g., collagen, fibronectin, and laminin) as well as binding partners on adjacent cells (e.g., VCAM-1 and PECAM-1) [10–13]. The physical link between these adhesion receptors and the actin cytoskeleton via intracellular focal adhesion proteins mediates the bidirectional force transmission and the biochemical signal transduction across the plasma membrane [14, 15]. The major signaling pathways activated by integrins through their α-subunits are different. The activation of α4 and α9 integrin subunits leads to decreased cell spreading and increased cell migration on a planar substrate [16–18]. This is in contrast to the activation of other integrin α-subunits (e.g., α1, α5, αv, α3, α6, and αIIb) that lead to enhanced cell spreading and decreased cell migration [19–23] and show different bindings to fibronectin via the canonical integrin recognition site arginine-glycine-aspartic acid (RGD) [24–28]. Furthermore, the α5β1 integrin regulates the αvβ3-mediated adhesions and migration on the extracellular matrix [29]. The formation, activation, and regulation of focal adhesion proteins in the focal adhesions and their physiological function are pivotal and have been the focus of intense research efforts and may have opposite effects depending on the integrin subunit type [9], but the mechano-regulating function, for example, in the process of cell invasion is still elusive. The αvβ3, αvβ6, and α6β4 integrins have been described to act as enhancers of tumor cell invasion and metastasis formation [30–32]. Their role in the process of metastasis formation and their impact on transendothelial migration of tumor cells are still unclear.

The β1 integrins have also been reported to promote tumor cell migration in a matrigel [33]. To make it more confusing, the role of the α5β1 in the process of 3D cell invasion, tumor growth and metastasis formation is controversially discussed because several reports described an invasion enhancing, tumor growth promoting, and metastasis increasing role that is inversely correlated with E-cadherin expression [34, 35], but others reported it vice versa [36–38]. The differences of the results might be explained by the use of different tumor cell lines. The correlation of the expression of one gene alone might not be helpful in determining the malignant potential of a tumor. The combination of gene expression and biophysical measurements of the cell's mechanical properties could be more sufficient because the expression a certain integrin by itself changes the cytoskeletal structure of a cell [39]. Combined with gene expression data, the overall cellular stiffness or the cytoskeletal dynamics of a cell could explain cellular behavior, for example, cell invasion and help to understand the general mechanisms important for the regulation of this process [6].

2.2. Role of The Extracellular Matrix Composition and Mechanical Properties of The Tissue

The mechanical properties of the extracellular matrix determine the gene expression patterns, the differentiation, proliferation, and cell mechanical properties [40–42]. The ability to generate forces might also be influenced by the mechanical properties of the 3D environment of the cell [43]. Furthermore, the environmental properties of the primary tumor might also determine the secondary tumor formation site maybe because of similar mechanical properties of the primary tumor tissue and the new metastasis formation site. Adhesion strength and cell stiffness determine the strength of the contractile forces [43] and might influence the ability of cells to invade into the extracellular matrix and to transmigrate through an endothelial cell monolayer and the basement membrane surrounding the vessels. The ability to remodel their cytoskeleton to squeeze through the pores of the extracellular matrix (amoeboid migration) with or without the generation of contractile forces is important for the invasion speed, invasion depth, and finally the ability to form metastasis. For the migration in a 3D matrix, the CSK-fluidity may play also an important role, the higher the CSK-fluidity the higher the invasiveness of the cells (Figure 2).

2.3. Enzymatic Modulation of The Mechanical Properties of A 3d Connective Tissue

Changes of the extracellular matrix composition and structure (e.g., matrix pore size) influence the mechanical parameters of the matrix that could impact cell invasiveness via changing the mechanical properties inside the cell. These changes of the extracellular matrix's mechanical properties could origin from the invading cell itself. For example, cell shape changes such as protrusion dynamics of mesenchymal tumor cells were monitored in combination with matrix deformation due to enzymatic matrix remodeling using a 3D collagen matrix embedded with polystyrene beads [44]. The cells themselves produce enzymes either membrane-bound (e.g., MT-MMPs) or secreted to modulate the adjacent extracellular matrix [33]. The expression of collagenases MMP-14, MMP-12, and MMP-9 increase the invasiveness of tumor cells migrating through a collagen fiber network or through a Boyden-chamber (transwell membrane) [33]. MMP-9 cooperates with the αvβ3 integrin in supporting breast carcinoma cell migration using transwell membrane assay [20]. The inhibition of these enzymes using a cocktail of inhibitors leads to reduced or impaired invasion of tumor cells and changes the prior mesenchymal invasion to an amoeboid invasion type [33]. The production of sheddases leads to the cleavage (e.g., ADAMs = a disintegrin and metalloprotease domain) of several adhesion receptors like α6 integrin and αvβ3 integrin, reduces cell adhesion, and increases motility [22, 45, 46]. ADAMs are a family of type I transmembrane glycoproteins that have the ability to bind to integrins and disrupt their adhesion to the extracellular matrix [47–49]. The ADAM-15 sheddase contains an RGD-peptide motif and can hence act as a natural binding partner for αvβ3 integrin and reduce cell adhesion, increasing migration and invasion of tumor cells [50]. Despite the binding to αvβ3 integrin, the ADAM-15 interacts also with the α5β1 integrin [51]. Hence, the expression of sheddases like ADAM-15 is associated with a poor diagnosis of the cancer disease [52] and supports the interaction of prostate cancer cells and endothelial cells in the process of metastasis formation [53]. Confirming that the overexpression of MMP-14 increased the invasiveness of the cells, more cells were able to invade and they invade deeper into the gel via enhanced motility (or a higher adhesion site turn over rate). The cutting of the extracellular part of membrane-bound receptors reduced their cell surface expression that leads to decreased adhesion strength and decreased traction generation. All these enzymes alter either the extracellular matrix adjacent to the invading cell or the adhesion receptor expression on the migrating cell itself. This might influence, in turn, the adhesion strength (e.g., the adhesion process) and the generation of contractile forces (Figure 2).

3. Interactions of Tumor Cells and Endothelial Cells

3.1. Transendothelial Migration: Intravasation and Extravasation of Tumor Cells

The metastasis formation process begins with the dissociation of single or clustered tumor cells from the primary tumor and is followed by extracellular matrix invasion, entrance into blood or lymph vessels (intravasation), and transport to other tissue sites of the body (Figure 1). It has been reported that tumor cells sometimes escape from the microvasculature (extravasation), invade into the tumor-type dependent specified target tissue, and form a secondary tumor in distant organs [3, 54, 55]. The mechanisms of the tumor-type specific targeting of secondary tumor formation are almost unknown. Some people speculate about mechanical properties of the tissues determining different target-organ selections for secondary tumor formation [56, 57]. The extravasation process as well as the intravasation process involves adhesion of tumor cells to endothelial cells and the transmigration through the endothelium and underlying basement membrane [3, 58–60]. For several tumor cell types, it has been reported that they are able to pass the endothelial barrier (perivascular metastasis) [60–65]. Nevertheless, the extravasation step is not the only mechanism for metastasis formation, it is also possible that tumor cells intravasate into vessels, but they never extravasate. These tumor cells grow inside the vessels on the endothelial cell layer and form the metastasis at these sites (intravascular metastasis) [4]. Despite the extravasation step performed, the function of the endothelial monolayer in the metastasis formation process is thought to be crucial in that it can actively regulate metastasis formation by either allowing or blocking the adhesion, and possibly transmigration, of tumor cells and thereby determining the target organ of secondary tumor formation [62–64]. The endothelial cell function in the process of metastasis formation is still unclear, and the effect of the endothelium even to promote tumor cell invasion has recently been reported, but the mechanism is poorly understood [6]. More insights might bring novel in vivo models on metastasis formation.

3.2. in Vivo Models: Vascular and Lymphatic Routes of Metastasis Formation

Metastasis formation occurs via the vascular system as well via the lymphatic system [4, 66–68]. Tumor cells can form intravascular and perivascular metastases [3, 4, 69] (Figure 1). Any type of cancer process, including tumor cell motility and invasion, as well as metastasis formation can be measured using animal models in combination with fluorescent proteins that stain the injected tumor cells as well as the host tissue. Naturally fluorescent proteins, especially those with long excitation wavelengths, visualize in real time, aspects of tumor initiation, tumor growth, and metastasis formation in living animals [66, 68, 70–73]. The benefit of these novel in vivo rodent metastasis models allows us to study migration directly in live blood or lymph vessels and tumor-host interactions in the presence or in the absence of anticancer drugs or chemotherapy drugs [67, 71, 74, 75]. Besides, the injection of tumor cells whole tissue explants (named orthotropic model) can be transferred into nude mice and studied for response to drugs or vascularization [71, 76]. These studies show that tumor cells metastasize via vascular and lympathic vessels [4, 66–68]. The lymphatic route (lymphatic system) of the tumor metastasis formation is less well understood compared to the vascular route (circulatory system) [77]. Using the real-time imaging of fluorescently labeled tumor cells that were injected in the inguinal lymph node, tumor cell survival and migration to the axillary lymph node were measured. In addition, the effect of pressure on tumor cell shedding into lymph vessels and migration to the lymph node was analyzed. Due to the clinical studies indicating that high interstitial fluid pressure in the tumor is correlated with a poor diagnosis [78–80], this lymphatic animal model shows that increased pressure on the tumor increased the numbers of shedded tumor cells that may lead to higher lymphatic metastasis formation [68]. The mechanical properties of the extracellular matrix (in this case of the tumor) change the cellular properties toward higher motility and invasiveness. A combination of these in vivo models with biophysical measurements will help to get more insights and reveal the mechanisms why some tumors metastasize and others do not and what role the endothelium plays.

3.3. Does The Endothelium Represent A Barrier for Tumor Cell Invasion?

It is still unclear whether tumor cells transmigrate through the cytoplasm of endothelial cells similar to leukocytes, or destroy endothelial cells [81], or transmigrate between two adjacent endothelial cells by Src-mediated disruption of their cell-cell connections (VE-cadherin-β-catenin) [61]. It has been reported that transmigrating tumor cells are able to overcome the endothelial barrier by inducing changes within the endothelial cell monolayer, including the upregulation of adhesion molecule receptor expression [82], the reorganization of the cytoskeleton [83], Src-mediated disruption of endothelial cell-cell-adhesions [61], the formation of “holes” within the endothelial layer [84], and the induction of apoptosis [81] (Figure 3). Furthermore, tumor cell invasion may use similar invasion strategies as leukocytes, for which the endothelium acts as a barrier and greatly reduces invasion rates [85].

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3.4. How Do Cell-Cell Adhesion Receptors Influence Tumor Cell Invasion?

Beside cell-matrix receptors, cell-cell adhesion receptors play a role in cell invasion and especially facilitate transendothelial migration of tumor cells as well as leukocytes. It has been reported that αvβ3 integrin as well as glycosylphatidylinositol-anchored CD24 protein facilitates tumor cell transmigration and enhances tumor cell invasion in a 3D collagen fiber network [6, 8, 86] (Figure 4). Endothelial cells expressed L1-CAM and PECAM-1 have been described as counter-receptors that interact with cancer cell αvβ3 integrin [87, 88]. Endothelial cells expressed L1-CAM, and P-selectin have been described as a ligands for CD24 [7, 89]. A loss of E-cadherin cell-cell contacts is important for single cell invasion and has recently been discovered as a tumor suppressor gene [5]. The α4β1 integrin interacts either with VCAM-1 or CD14 to enhance tumor cell migration or invasion [11, 90]. It has to be ruled out how the interaction of tumor cells and endothelial cells through these receptors might, in turn, alter the mechanical properties of both cell types and change their invasive potential.

3.5. Role of Cytokines, Chemokines, or Other Stimuli in Tumor Cell Invasion and Transmigration

The scatter factor/hepatocyte growth factor (HGF) has largely been analyzed to enhance tumor cell migration on 2D substrates in in vitro cell culture assays [91]. Consistent to in vitro experiments, in vivo experiments have shown that this factor increased tumor cell spreading, dissemination, and metastasis formation in mice [91]. Recently, it has been shown that HGF influences the expression of integrin receptors, which in turn mediates the secretion of MMPs [92]. Despite this interaction, HGF ligand binding to the Met receptor as well as the α6β4 integrin can independently enhance tumor cell invasion [32].

Cytokines affect the barrier function of an endothelial cell monolayer (Figure 5). For example, the function of the endothelial cell barrier against both leukocyte trafficking and tumor cell transmigration is reduced in the presence of inflammatory cytokines like such as necrosis factor-α and interleukin-1β [62, 82, 93, 94]. These cytokines induce an upregulation of the cell-cell adhesion molecule E-selectin [82]. The subsequent adhesion of tumor cells expressing the E-selectin counter-receptor sialyl Lewis x (CD15s) to endothelial E-selectin leads to an upregulation of stress-activated protein kinase-2 (SAPK2/p38) in endothelial cells [82] and triggers actin polymerization and actin reorganization into stress fibers [83] (Figure 4).

Chemokines and their receptors have an impact on leukocyte trafficking [95, 96] and tumor cell invasion [97]. The superfamily of chemokines consists of small cytokine-like proteins that induce cytoskeletal rearrangements in endothelial cells and leukocytes, the firm adhesion of leukocytes to endothelial cells, and the directional migration (chemotaxis) of leukocytes [95]. The involvement of chemokines in tumor-endothelial interactions and their effect on tumor cell mechanical properties during invasion are considerably less well understood.

We recently found that the expression of the chemokine receptor CXCR2 enhanced tumor cell motility in 3D extracellular collagen matrix. The expression of the CXCR2 influences other mechanical properties of the receptor bearing cells [6]. High CXCR2 expressing subcell lines derived from the human breast carcinoma cells MDA-MB-231 produced enhanced traction forces on fibronectin-coated 2D substrates [6]. CSK-dynamics, cell stiffness, and CSK-fluidity are enhanced [6].

Another impact of the CXCR2 receptor in the metastasis formation process could be the interaction with endothelial cells producing the CXCR2 ligands Gro-β and IL-8. Both chemokines enhance the transmigration and the followed invasiveness in vitro 3-D collagen fiber matrix assays [6]. Recently, it has been reported that Gro-β and IL-8 receptor (CXCR2) expressions on tumor cells are the key mediators responsible for the breakdown of the endothelial barrier function by enhancing tumor cell force generation and cytoskeletal remodeling dynamics (Figure 6). These results have to be expanded on other tumor cell types and further improved by using animal metastases models. All these different stimulations of the cells might underlie a common change of the cell's mechanical properties.

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4. Role of Other Cell Types during Metastasis Formation

Several recent reports discussed the importance of platelets in adhering to single tumor cells and promote or induce their transendothelial migration [98–100], but in contrast to them, many other reports show clearly that single tumor cells are by themselves able to transmigrate through the endothelium [6–8, 62]. The platelets might be able to decorate single tumor cells and enhance their transmigration and invasion capabilities. But the question of do other cell types promote or induce tumor cell invasion and metastasis formation is still not answered fully. Do platelets guide tumor cells through the endothelium? For example, the role of mast cells either in solid tumors or in close neighborhood to tumors is poorly investigated. Did mast cells also promote or induce tumor cell transmigration or invasion? Do mast cells stimulate tumor cells to contract after histamine release? It has been reported that mast cells survive in close contact to endothelial cells and even proliferate there [101]. This might explain the increased numbers of mast cells in vascularized solid tumors [102–104]. Of course other cell types like eosinophilic granulocytes, lymphocytes, or monocytes/macrophages might also influence the mechanical properties of tumor cells either by secretion of contractile force stimulating (enhancing) or by relaxing the substances. The role of mast cells in tumor metastasis formation has to be ruled out by using biophysical tools as well as dual-color imaging animal metastasis models.

The presence of macrophages in a tumor has been correlated with a poor prognosis, but how macrophages are involved in hematogenous metastasis was unclear. Do macrophages change the mechanical properties of the tumor cells either by direct binding or by secretion of cytokines or by growth factors? Direct visualization of macrophages that assisted tumor cell intravasation in hematogenous metastasis of mammary tumors has been reported by using multiphoton microscopy [105]. Macrophages supported tumor cell motility toward blood vessels and tumor cell intravasation [105]. How this affects the mechanical properties of the tumor cells and their ability to generate contractile forces to move forward remain unclear and should be further investigated using biophysical tools, for example, traction microscopy. The dual-color fluorescence imaging technology distinguishes injected and fluorescently labeled tumor cells from the host stroma cells of transgenic mice and enables further insights in tumor-host interactions [106, 107].

5. Contractile Forces and the Role of Vinculin

5.1. Measurement of Contractile Forces

To move forward in a 3D matrix, the invading tumor cells need to generate contractile forces to overcome the viscous drag. Despite the composition and the enzymatic digestion of the matrix, the coordinated regulation of cell adhesion (adhesion strength) and deadhesion (including cytoskeletal remodeling) together with the generation of contractile forces determine the invasion speed in a 3D matrix. Our knowledge of cell migration, mechanical tensions, and forces is derived from studies of cells cultured on planar substrates (e.g., glass or polyacrylamide hydrogels). Previous reports showed how to measure traction forces during cell migration in 2D culture systems [108, 109] and were further improved to quantitative tools [110–113]. All the methods depend on the measurement of the deformations of an elastic substrate with known elastic modulus on which the cells adhered and spread. During this cell-matrix contact, the cell generates tractions and deforms the substrate. The tractions were computed from the substrate displacements visualized by embedded markers (fluorescent 0.5 m beads) using continuum mechanics theory. Measurement of the displacement field is accomplished by tracking these beads that are near the surface of the substrate. The spatial resolution of the traction map obtained with traction microscopy approaches is 1 m, which is sufficient to resolve the forces from individual focal adhesions [112]. Traction microscopy has brought new insights into tumor cell migration in particular [6, 86, 113]. The cells feel and respond to the stiffness of the extracellular matrix through dynamic regulation of integrin clustering, altered focal adhesion formation, and remodeling of the cell's cytoskeleton [40]. To conclude, contractile force generation and cell invasion are strongly influenced by the mechanical properties of the extracellular matrix [109].

5.2. Cell-Matrix Adhesions Protein Vinculin

For the generation of contractile forces, a cell needs to adhere to the 3D matrix via cell-matrix adhesions. The focal adhesion protein vinculin has been described to be structurally important connecting the extracellular matrix via cell-matrix adhesions and adjacent cells via cell-cell adhesions with the actin cytoskeleton by providing an intracellular linkage between the integrin receptor and the actin cytoskeleton via the focal adhesion formation [114–117]. The vinculin protein is encoded by 1066 amino acids, has a molecular weight of ~117 kDa, and binds to many other focal adhesion and cytoskeletal proteins including talin, paxillin, tensin, zyxin, VASP, α-actinin and actin [118].

The function of vinculin has been largely analyzed in cells cultured in 2D systems. Vinculin knock out (k.o.) mouse embryonic fibroblasts (MEFs) as well as vinculin k.o. mouse embryonic carcinoma cells (F9 cells) exhibit a more round cell shape, show fewer and less stable lamellipodia, but similar filopodia compared to vinculin-expressing MEFs (wild type) [116, 119, 120]. Focal adhesion complexes of vin-/- cells are smaller and consist of increased tyrosine-phosphorylated proteins like talin, α-actinin, FAK, and paxillin without increasing total protein content [116, 121]. Vinculin-deficient fibroblasts (MEFvin-/-) and carcinoma cells (vin-/-) show reduced adhesion to extracellular matrix proteins like fibronectin, vitronectin, laminin, and collagen as well as a two-fold increase in motility and three-fold increase in focal adhesion kinase activity compared to wild-type cells [121, 122]. All the described studies were performed in 2D migration or 2D adhesion assays and did not properly mirror the in vivo situation of cells invading and contracting the 3D tissue environment during the malignant progression of tumor disease involving tumor outgrowth and metastasis formation.

Vinculin's function in tumor disease has so far hardly been investigated. We recently reported that vinculin functions as a mechano-coupling protein, and that its tail-domain acts as a regulator for contractile force generation [86].

In a recent study, we examined whether vinculin is involved in cell invasion into a 3D extracellular matrix [123]. We found that vinculin enhanced the generation of tractions, and that this mechanical parameter despite all other mechanical parameters (e.g., cell adhesion, detachment, and matrix degradation) plays a prominent role in cell invasion in a 3D matrix to overcome the steric hindrances, but not on a 2D substrate, where the viscous drag is negligible. Future analyzes of the transmission of forces in cells via focal adhesions might help to determine the prerequisites of the invasive potential of a tumor cell.

6. How Can Mechanical Parameters of the Cells Help to Improve Tumor Diagnosis?

Several reports describe a relationship between tumor cell mechanical properties and their malignant potential in promoting metastasis formation [6, 43, 124]. The measurement of only a single cell mechanical parameter might not be sufficient to predict the invasiveness of tumor cells nor their metastasis formation potential. Many factors may be involved in promoting tumor cell invasion (Figure 2) and tumor cell transendothelial formation (Figure 5). The mechanical properties of the tumor cells as well as their adhesion receptor, sheddases, or enzyme expressions together determine the ability to invade a tissue and to transmigrate the endothelium (Figures 2 and 5). Only small fraction of tumor cell lines is able to invade a 3D extracellular matrix [6]. To provide a proper analysis tool to determine the invasive or metastasis potential of a tumor, it is first important to isolate subcell fractions of isolated primary tumor cells using well-defined mechanical parameters (contractile force generation). These obtained primary tumor cells can be analyzed for their metastatic potential by using metastatic animal models.

7. Role of Clinically Relevant Metastatic Animal Models

Orthotropic metastatic animal models can be used to discover anticancer drugs and to determine drugs' efficiency [71]. These models are established for a wide variety of tumors including spontaneous metastatic bone models of prostate cancer, breast cancer, and lung cancer as well as spontaneous liver and lymph node metastastic models of colon, pancreatic, stomach, ovarian, bladder, and kidney cancer [71]. These models present a new generation of rodent tumor models and differ from transgenic tumor models or subcuntanenously-growing human tumors in immunodeficient mice, because the latter models did not represent sufficient models in regard to metastasis formation or drug sensitivity [71]. The advantage of novel orthotropic metastatic models is that histologically intact fragments of human cancer—directly taken from the patient—were implanted to the corresponding organ of immunodeficient mice. This allows researchers to determine tumor growth and metastatic potential of transplanted tumors [125, 126]. These orthotropic metastatic animal models can be combined with measurements of the cells mechanical properties and the mechanical properties of the transplanted tissue. To understand the diverse roles of the endothelium in the tumor metastasis, a transgenic nude mouse model visualizing tumor angiogenesis could be helpful. It is based on the nestin-promotor-linked green fluorescent protein because many of the newly formed blood vessels originate from hair-follicle stem cells that express nestin. The transcription of GFP indicates newly formed blood vessels in the animal [127].

8. Conclusions and Future Directions

In summary, this paper presented a new function of the endothelium in inducing or enhancing tumor cell invasion. It discussed the two described pathways for tumor cell metastasis formation and pointed out the importance of cell-matrix and cell-cell adhesion receptors as well as chemokine receptors for tumor-endothelial cell interactions. It focused the view on the mechanical properties of tumor cells as well as that of endothelial cells during the process of metastasis formation. It discussed in vivo animal models to visualize vascular and lymphoid metastases formation of single injected tumor cells or implanted orthotropic tissue resections.

The main new direction of tumor cell invasion and metastasis research is to measure the ability of tumor cells to generate contractile forces in a 3D environment and to determine the malignancy of a tumor using in vivo animal models. The mechanical measurements of tumor cell subpopulations in patient's liquids or tissue samples might help to determine whether a tumor is able to form metastases. A future direction of tumor metastasis research is to focus on the diverse roles of the endothelium. The combination of biophysical tools for mechanical properties analysis of tumor and endothelial cells, the generation of mechanical diverse tumor cells, and with their injection into nude mice using the dual-color in vivo imaging method will be extremely helpful in developing new diagnosis tools and drugs reducing tumor metastases.

Acknowledgments

This work was supported by the Deutsche Krebshilfe (107384) and DFG (FA336/2-1).

References

C. Lengauer, K. W. Kinzler, and B. Vogelstein, “Genetic instabilities in human cancers,” Nature, vol. 396, no. 6712, pp. 643–649, 1998.
View at: Publisher Site | Google Scholar
F. C. Bender, M. A. Reymond, C. Bron, and A. F. Quest, “Caveolin-1 levels are down-regulated in human colon tumors, and ectopic expression of caveolin-1 in colon carcinoma cell lines reduces cell tumorigenicity,” Cancer Research, vol. 60, no. 20, pp. 5870–5878, 2000.
View at: Google Scholar
P. S. Steeg, “Tumor metastasis: mechanistic insights and clinical challenges,” Nature Medicine, vol. 12, no. 8, pp. 895–904, 2006.
View at: Publisher Site | Google Scholar
A. B. Al-Mehdi, K. Tozawa, A. B. Fisher, L. Shientag, A. Lee, and R. J. Muschel, “Intravascular origin of metastasis from the proliferation of endothelium-attached tumor cells: a new model for metastasis,” Nature Medicine, vol. 6, no. 1, pp. 100–102, 2000.
View at: Publisher Site | Google Scholar
U. H. Frixen, J. Behrens, M. Sachs et al., “E-cadherin-mediated cell-cell adhesion prevents invasiveness of human carcinoma cells,” The Journal of Cell Biology, vol. 113, no. 1, pp. 173–185, 1991.
View at: Publisher Site | Google Scholar
C. T. Mierke, D. P. Zitterbart, P. Kollmannsberger et al., “Breakdown of the endothelial barrier function in tumor cell transmigration,” Biophysical Journal, vol. 94, no. 7, pp. 2832–2846, 2008.
View at: Publisher Site | Google Scholar
S. Runz, C. T. Mierke, S. Joumaa, J. Behrens, B. Fabry, and P. Altevogt, “CD24 induces localization of $β$ 1 integrin to lipid raft domains,” Biochemical and Biophysical Research Communications, vol. 365, no. 1, pp. 35–41, 2008.
View at: Publisher Site | Google Scholar
K. Bauer, C. T. Mierke, and J. Behrens, “Expression profiling reveals genes associated with transendothelial migration of tumor cells: a functional role for $α$ v $β$ 3 integrin,” International Journal of Cancer, vol. 121, no. 9, pp. 1910–1918, 2007.
View at: Publisher Site | Google Scholar
F. G. Giancotti, “Complexity and specificity of integrin signalling,” Nature Cell Biology, vol. 2, no. 1, pp. E13–E14, 2000.
View at: Publisher Site | Google Scholar
C. Marcinkiewicz, Y. Taooka, Y. Yokosaki et al., “Inhibitory effects of MLDG-containing heterodimeric disintegrins reveal distinct structural requirements for interaction of the integrin $a$ 9 $ß$ 1 with VCAM-1, tenascin-C, and osteopontin,” The Journal of Biological Chemistry, vol. 275, no. 41, pp. 31930–31937, 2000.
View at: Publisher Site | Google Scholar
M. Klemke, T. Weschenfelder, M. H. Konstandin, and Y. Samstag, “High affinity interaction of integrin $α$ 4 $β$ 1 (VLA-4) and vascular cell adhesion molecule 1 (VCAM-1) enhances migration of human melanoma cells across activated endothelial cell layers,” Journal of Cellular Physiology, vol. 212, no. 2, pp. 368–374, 2007.
View at: Publisher Site | Google Scholar
E. B. Voura, N. Chen, and C.-H. Siu, “Platelet-endothelial cell adhesion molecule-1 (CD31) redistributes from the endothelial junction and is not required for the transendothelial migration of melanoma cells,” Clinical and Experimental Metastasis, vol. 18, no. 6, pp. 527–532, 2000.
View at: Publisher Site | Google Scholar
R. O. Hynes, “Integrins: bidirectional, allosteric signaling machines,” Cell, vol. 110, no. 6, pp. 673–687, 2002.
View at: Publisher Site | Google Scholar
W. H. Goldmann, R. M. Ezzell, E. D. Adamson, V. Niggli, and G. Isenberg, “Vinculin, talin and focal adhesions,” Journal of Muscle Research and Cell Motility, vol. 17, no. 1, pp. 1–5, 1996.
View at: Publisher Site | Google Scholar
W. H. Goldmann, “The coupling of vinculin to the cytoskeleton is not essential for mechano-chemical signaling in F9 cells,” Cell Biology International, vol. 26, no. 3, pp. 279–286, 2002.
View at: Publisher Site | Google Scholar
S. Liu and M. H. Ginsberg, “Paxillin binding to a conserved sequence motif in the $α_{4}$ integrin cytoplasmic domain,” The Journal of Biological Chemistry, vol. 275, no. 30, pp. 22736–22742, 2000.
View at: Publisher Site | Google Scholar
B. A. Young, Y. Taooka, S. Liu et al., “The cytoplasmic domain of the integrin $a$ 9 subunit requires the adaptor protein paxillin to inhibit cell spreading but promotes cell migration in a paxillin-independent manner,” Molecular Biology of the Cell, vol. 12, no. 10, pp. 3214–3225, 2001.
View at: Google Scholar
S. Liu, M. Slepak, and M. H. Ginsberg, “Binding of paxillin to the $α_{9}$ integrin cytoplasmic domain inhibits cell spreading,” The Journal of Biological Chemistry, vol. 276, no. 40, pp. 37086–37092, 2001.
View at: Publisher Site | Google Scholar
A. R. Horwitz and J. T. Parsons, “Cell migration—movin' on,” Science, vol. 286, no. 5442, pp. 1102–1103, 1999.
View at: Publisher Site | Google Scholar
M. Rolli, E. Fransvea, J. Pilch, A. Saven, and B. Felding-Habermann, “Activated integrin $α$ v $β$ 3 cooperates with metalloproteinase MMP-9 in regulating migration of metastatic breast cancer cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 16, pp. 9482–9487, 2003.
View at: Publisher Site | Google Scholar
R. S. Schmid, S. Shelton, A. Stanco, Y. Yokota, J. A. Kreidberg, and E. S. Anton, “ $α$ 3 $β$ 1 integrin modulates neuronal migration and placement during early stages of cerebral cortical development,” Development, vol. 131, no. 24, pp. 6023–6031, 2004.
View at: Publisher Site | Google Scholar
S. C. Pawar, M. C. Demetriou, R. B. Nagle, G. T. Bowden, and A. E. Cress, “Integrin $α$ 6 cleavage: a novel modification to modulate cell migration,” Experimental Cell Research, vol. 313, no. 6, pp. 1080–1089, 2007.
View at: Publisher Site | Google Scholar
U. K. Rout, J. Wang, B. C. Paria, and D. R. Armant, “ $α$ 5 $β$ 1, $α$ V $β$ 3 and the platelet-associated integrin $α$ IIb $β$ 3 coordinately regulate adhesion and migration of differentiating mouse trophoblast cells,” Developmental Biology, vol. 268, no. 1, pp. 135–151, 2004.
View at: Publisher Site | Google Scholar
D. D. Hu, J. R. Hoyer, and J. W. Smith, “ ${Ca}^{2 +}$ suppresses cell adhesion to osteopontin by attenuating binding affinity for integrin $α_{v} β_{3}$ ,” The Journal of Biological Chemistry, vol. 270, no. 17, pp. 9917–9925, 1995.
View at: Publisher Site | Google Scholar
L. Liaw, V. Lindner, S. M. Schwartz, A. F. Chambers, and C. M. Giachelli, “Osteopontin and $β$ 3 integrin are coordinately expressed in regenerating endothelium in vivo and stimulate Arg-Gly-Asp-dependent endothelial migration in vitro,” Circulation Research, vol. 77, no. 4, pp. 665–672, 1995.
View at: Google Scholar
A. Miyauchi, J. Alvarez, E. M. Greenfield et al., “Recognition of osteopontin and related peptides by an $a_{v} ß_{3}$ integrin stimulates immediate cell signals in osteoclasts,” The Journal of Biological Chemistry, vol. 266, no. 30, pp. 20369–20374, 1991.
View at: Google Scholar
S. T. Barry, S. B. Ludbrook, E. Murrison, and C. M. T. Horgan, “Analysis of the $α$ 4 $β$ 1 integrin-osteopontin interaction,” Experimental Cell Research, vol. 258, no. 2, pp. 342–351, 2000.
View at: Publisher Site | Google Scholar
K. Nasu, T. Ishida, M. Setoguchi, Y. Higuchi, S. Akizuki, and S. Yamamoto, “Expression of wild-type and mutated rabbit osteopontin in Escherichia coli, and their effects on adhesion and migration of P388D1 cells,” Biochemical Journal, vol. 307, part 1, pp. 257–265, 1995.
View at: Google Scholar
D. P. Ly, K. M. Zazzali, and S. A. Corbett, “De novo expression of the integrin $α_{5} β_{1}$ regulates $α_{v} β_{3}$ -mediated adhesion and migration on fibrinogen,” The Journal of Biological Chemistry, vol. 278, no. 24, pp. 21878–21885, 2003.
View at: Publisher Site | Google Scholar
B. Felding-Habermann, T. E. O'Toole, J. W. Smith et al., “Integrin activation controls metastasis in human breast cancer,” Proceedings of the National Academy of Sciences of the United States of America, vol. 98, no. 4, pp. 1853–1858, 2001.
View at: Publisher Site | Google Scholar
M. L. Nystrom, D. McCulloch, P. H. Weinreb et al., “Cyclooxygenase-2 inhibition suppresses $a_{v} ß_{6}$ integrin-dependent oral squamous carcinoma invasion,” Cancer Research, vol. 66, no. 22, pp. 10833–10842, 2006.
View at: Publisher Site | Google Scholar
J. Chung, S.-O. Yoon, E. A. Lipscomb, and A. M. Mercurio, “The Met receptor and $α_{6} β_{4}$ integrin can function independently to promote carcinoma invasion,” The Journal of Biological Chemistry, vol. 279, no. 31, pp. 32287–32293, 2004.
View at: Publisher Site | Google Scholar
K. Wolf, I. Mazo, H. Leung et al., “Compensation mechanism in tumor cell migration: mesenchymal-amoeboid transition after blocking of pericellular proteolysis,” The Journal of Cell Biology, vol. 160, no. 2, pp. 267–277, 2003.
View at: Publisher Site | Google Scholar
F. Qian, Z.-C. Zhang, X.-F. Wu, Y.-P. Li, and Q. Xu, “Interaction between integrin $α_{5}$ and fibronectin is required for metastasis of B16F10 melanoma cells,” Biochemical and Biophysical Research Communications, vol. 333, no. 4, pp. 1269–1275, 2005.
View at: Publisher Site | Google Scholar
K. Sawada, A. K. Mitra, A. R. Radjabi et al., “Loss of E-cadherin promotes ovarian cancer metastasis via $a$ 5-integrin, which is a therapeutic target,” Cancer Research, vol. 68, no. 7, pp. 2329–2339, 2008.
View at: Publisher Site | Google Scholar
D. Taverna, M. Ullman-Culleré, H. Rayburn, R. T. Bronson, and R. O. Hynes, “A test of the role of $α$ 5 integrin/fibronectin interactions in tumorigenesis,” Cancer Research, vol. 58, no. 4, pp. 848–853, 1998.
View at: Google Scholar
M. Schirner, F. Herzberg, R. Schmidt et al., “Integrin $a$ 5 $ß$ 1: a potent inhibitor of experimental lung metastasis,” Clinical and Experimental Metastasis, vol. 16, no. 5, pp. 427–435, 1998.
View at: Publisher Site | Google Scholar
N. Tani, S. Higashiyama, N. Kawaguchi et al., “Expression level of integrin $a$ 5 on tumour cells affects the rate of metastasis to the kidney,” British Journal of Cancer, vol. 88, no. 2, pp. 327–333, 2003.
View at: Publisher Site | Google Scholar
S. Havaki, M. Kouloukoussa, K. Amawi et al., “Altered expression pattern of integrin $a$ v $ß$ 3 correlates with actin cytoskeleton in primary cultures of human breast cancer,” Cancer Cell International, vol. 7, article 16, pp. 1–13, 2007.
View at: Publisher Site | Google Scholar
D. E. Discher, P. Janmey, and Y.-L. Wang, “Tissue cells feel and respond to the stiffness of their substrate,” Science, vol. 310, no. 5751, pp. 1139–1143, 2005.
View at: Publisher Site | Google Scholar
N. Q. Balaban, U. S. Schwarz, D. Riveline et al., “Force and focal adhesion assembly: a close relationship studied using elastic micropatterned substrates,” Nature Cell Biology, vol. 3, no. 5, pp. 466–472, 2001.
View at: Publisher Site | Google Scholar
F. Rehfeldt, A. J. Engler, A. Eckhardt, F. Ahmed, and D. E. Discher, “Cell responses to the mechanochemical microenvironment-implications for regenerative medicine and drug delivery,” Advanced Drug Delivery Reviews, vol. 59, no. 13, pp. 1329–1339, 2007.
View at: Publisher Site | Google Scholar
I. L. Novak, B. M. Slepchenko, A. Mogilner, and L. M. Loew, “Cooperativity between cell contractility and adhesion,” Physical Review Letters, vol. 93, no. 26, Article ID 268109, 4 pages, 2004.
View at: Publisher Site | Google Scholar
R. J. Bloom, J. P. George, A. Celedon, S. X. Sun, and D. Wirtz, “Mapping local matrix remodeling induced by a migrating tumor cell using three-dimensional multiple-particle tracking,” Biophysical Journal, vol. 95, no. 8, pp. 4077–4088, 2008.
View at: Publisher Site | Google Scholar
B. I. Ratnikov, D. V. Rozanov, T. I. Postnova et al., “An alternative processing of integrin $a_{v}$ subunit in tumor cells by membrane type-1 matrix metalloproteinase,” The Journal of Biological Chemistry, vol. 277, no. 9, pp. 7377–7385, 2002.
View at: Publisher Site | Google Scholar
E. I. Deryugina, M. A. Bourdon, K. Jungwirth, J. W. Smith, and A. Y. Strongin, “Functional activation of integrin $α$ v $β$ 3 in tumor cells expressing membrane-type 1 matrix metalloproteinase,” International Journal of Cancer, vol. 86, no. 1, pp. 15–23, 2000.
View at: Publisher Site | Google Scholar
G. Weskamp and C. P. Blobel, “A family of cellular proteins related to snake venom disintegrins,” Proceedings of the National Academy of Sciences of the United States of America, vol. 91, no. 7, pp. 2748–2751, 1994.
View at: Publisher Site | Google Scholar
T. G. Wolfsberg, P. D. Straight, R. L. Gerena et al., “ADAM, a widely distributed and developmentally regulated gene family encoding membrane proteins wit a disintegrin and metalloprotease domain,” Developmental Biology, vol. 169, no. 1, pp. 378–383, 1995.
View at: Publisher Site | Google Scholar
T. G. Wolfsberg and J. M. White, “ADAMs in fertilization and development,” Developmental Biology, vol. 180, no. 2, pp. 389–401, 1996.
View at: Publisher Site | Google Scholar
V. Beck, H. Herold, A. Benge et al., “ADAM15 decreases integrin $a$ v $ß$ 3/vitronectin-mediated ovarian cancer cell adhesion and motility in an RGD-dependent fashion,” International Journal of Biochemistry & Cell Biology, vol. 37, no. 3, pp. 590–603, 2005.
View at: Publisher Site | Google Scholar
D. Nath, P. M. Slocombe, P. E. Stephens et al., “Interaction of metargidin (ADAM-15) with $a$ v $ß$ 3 and $a$ 5 $ß$ 1 integrins on different haemopoietic cells,” Journal of Cell Science, vol. 112, part 4, pp. 579–587, 1999.
View at: Google Scholar
R. Kuefer, K. C. Day, C. G. Kleer et al., “ADAM15 disintegrin is associated with aggressive prostate and breast cancer disease,” Neoplasia, vol. 8, no. 4, pp. 319–329, 2006.
View at: Publisher Site | Google Scholar
A. J. Najy, K. C. Day, and M. L. Day, “ADAM15 supports prostate cancer metastasis by modulating tumor cell-endothelial cell interaction,” Cancer Research, vol. 68, no. 4, pp. 1092–1099, 2008.
View at: Publisher Site | Google Scholar
L. A. Liotta, P. S. Steeg, and W. G. Stetler-Stevenson, “Cancer metastasis and angiogenesis: an imbalance of positive and negative regulation,” Cell, vol. 64, no. 2, pp. 327–336, 1991.
View at: Publisher Site | Google Scholar
R. R. Langley and I. J. Fidler, “Tumor cell-organ microenvironment interactions in the pathogenesis of cancer metastasis,” Endocrine Reviews, vol. 28, no. 3, pp. 297–321, 2007.
View at: Publisher Site | Google Scholar
L. Zhang, E. Giraudo, J. A. Hoffman, D. Hanahan, and E. Ruoslahti, “Lymphatic zip codes in premalignant lesions and tumors,” Cancer Research, vol. 66, no. 11, pp. 5696–5706, 2006.
View at: Publisher Site | Google Scholar
P. Laakkonen, K. Porkka, J. A. Hoffman, and E. Ruoslahti, “A tumor-homing peptide with a targeting specificity related to lymphatic vessels,” Nature Medicine, vol. 8, no. 7, pp. 751–755, 2002.
View at: Publisher Site | Google Scholar
G. L. Nicolson, “Metastatic tumor cell interactions with endothelium, basement membrane and tissue,” Current Opinion in Cell Biology, vol. 1, no. 5, pp. 1009–1019, 1989.
View at: Publisher Site | Google Scholar
W. G. Stetler-Stevenson, S. Aznavoorian, and L. A. Liotta, “Tumor cell interactions with the extracellular matrix during invasion and metastasis,” Annual Review of Cell Biology, vol. 9, pp. 541–573, 1993.
View at: Publisher Site | Google Scholar
K. J. Luzzi, I. C. MacDonald, E. E. Schmidt et al., “Multistep nature of metastatic inefficiency: dormancy of solitary cells after successful extravasation and limited survival of early micrometastases,” American Journal of Pathology, vol. 153, no. 3, pp. 865–873, 1998.
View at: Google Scholar
S. Weis, J. Cui, L. Barnes, and D. Cheresh, “Endothelial barrier disruption by VEGF-mediated Src activity potentiates tumor cell extravasation and metastasis,” The Journal of Cell Biology, vol. 167, no. 2, pp. 223–229, 2004.
View at: Publisher Site | Google Scholar
E. B. Voura, R. A. Ramjeesingh, A. M. P. Montgomery, and C.-H. Siu, “Involvement of integrin $α_{v} β_{3}$ and cell adhesion molecule L1 in transendothelial migration of melanoma cells,” Molecular Biology of the Cell, vol. 12, no. 9, pp. 2699–2710, 2001.
View at: Google Scholar
P.-L. Tremblay, F. A. Auger, and J. Huot, “Regulation of transendothelial migration of colon cancer cells by E-selectin-mediated activation of p38 and ERK MAP kinases,” Oncogene, vol. 25, no. 50, pp. 6563–6573, 2006.
View at: Publisher Site | Google Scholar
M. Sandig, E. B. Voura, V. I. Kalnins, and C.-H. Siu, “Role of cadherins in the transendothelial migration of melanoma cells in culture,” Cell Motility and the Cytoskeleton, vol. 38, no. 4, pp. 351–364, 1997.
View at: Publisher Site | Google Scholar
I. J. Fidler and I. R. Hart, “Biological diversity in metastatic neoplasms: origins and implications,” Science, vol. 217, no. 4564, pp. 998–1003, 1982.
View at: Publisher Site | Google Scholar
K. Yamauchi, M. Yang, P. Jiang et al., “Real-time in vivo dual-color imaging of intracapillary cancer cell and nucleus deformation and migration,” Cancer Research, vol. 65, no. 10, pp. 4246–4252, 2005.
View at: Publisher Site | Google Scholar
K. Yamauchi, M. Yang, K. Hayashi et al., “Induction of cancer metastasis by cyclophosphamide pretreatment of host mice: an opposite effect of chemotherapy,” Cancer Research, vol. 68, no. 2, pp. 516–520, 2008.
View at: Publisher Site | Google Scholar
K. Hayashi, P. Jiang, K. Yamauchi et al., “Real-time imaging of tumor-cell shedding and trafficking in lymphatic channels,” Cancer Research, vol. 67, no. 17, pp. 8223–8228, 2007.
View at: Publisher Site | Google Scholar
K. Tsuji, K. Yamauchi, M. Yang et al., “Dual-color imaging of nuclear-cytoplasmic dynamics, viability, and proliferation of cancer cells in the portal vein area,” Cancer Research, vol. 66, no. 1, pp. 303–306, 2006.
View at: Publisher Site | Google Scholar
R. M. Hoffman, “The multiple uses of fluorescent proteins to visualize cancer in vivo,” Nature Reviews Cancer, vol. 5, no. 10, pp. 796–806, 2005.
View at: Publisher Site | Google Scholar
R. M. Hoffman, “Orthotopic metastatic mouse models for anticancer drug discovery and evaluation: a bridge to the clinic,” Investigational New Drugs, vol. 17, no. 4, pp. 343–359, 1999.
View at: Publisher Site | Google Scholar
M. Bouvet, K. Tsuji, M. Yang, P. Jiang, A. R. Moossa, and R. M. Hoffman, “In vivo color-coded imaging of the interaction of colon cancer cells and splenocytes in the formation of liver metastases,” Cancer Research, vol. 66, no. 23, pp. 11293–11297, 2006.
View at: Publisher Site | Google Scholar
K. Yamauchi, M. Yang, P. Jiang et al., “Development of real-time subcellular dynamic multicolor imaging of cancer-cell trafficking in live mice with a variable-magnification whole-mouse imaging system,” Cancer Research, vol. 66, no. 8, pp. 4208–4214, 2006.
View at: Publisher Site | Google Scholar
M. Yang, J. Reynoso, P. Jiang, L. Li, A. R. Moossa, and R. M. Hoffman, “Transgenic nude mouse with ubiquitous green fluorescent protein expression as a host for human tumors,” Cancer Research, vol. 64, no. 23, pp. 8651–8656, 2004.
View at: Publisher Site | Google Scholar
Y. Amoh, L. Li, M. Yang et al., “Hair follicle-derived blood vessels vascularize tumors in skin and are inhibited by doxorubicin,” Cancer Research, vol. 65, no. 6, pp. 2337–2343, 2005.
View at: Publisher Site | Google Scholar
Y. Amoh, L. Li, K. Tsuji et al., “Dual-color imaging of nascent blood vessels vascularizing pancreatic cancer in an orthotopic model demonstrates antiangiogenesis efficacy of gemcitabine,” Journal of Surgical Research, vol. 132, no. 2, pp. 164–169, 2006.
View at: Publisher Site | Google Scholar
S. D. Nathanson, “Insights into the mechanisms of lymph node metastasis,” Cancer, vol. 98, no. 2, pp. 413–423, 2003.
View at: Publisher Site | Google Scholar
B. D. Curti, W. J. Urba, W. G. Alvord et al., “Interstitial pressure of subcutaneous nodules in melanoma and lymphoma patients: changes during treatment,” Cancer Research, vol. 53, no. 10, pp. 2204–2207, 1993.
View at: Google Scholar
H. D. Roh, Y. Boucher, S. Kalnicki, R. Buchsbaum, W. D. Bloomer, and R. K. Jain, “Interstitial hypertension in carcinoma of uterine cervix in patients: possible correlation with tumor oxygenation and radiation response,” Cancer Research, vol. 51, no. 24, pp. 6695–6698, 1991.
View at: Google Scholar
M. Milosevic, A. Fyles, D. Hedley et al., “Interstitial fluid pressure predicts survival in patients with cervix cancer independent of clinical prognostic factors and tumor oxygen measurements,” Cancer Research, vol. 61, no. 17, pp. 6400–6405, 2001.
View at: Google Scholar
C. Heyder, E. Gloria-Maercker, F. Entschladen et al., “Realtime visualization of tumor cell/endothelial cell interactions during transmigration across the endothelial barrier,” Journal of Cancer Research and Clinical Oncology, vol. 128, no. 10, pp. 533–538, 2002.
View at: Publisher Site | Google Scholar
J. Laferrière, F. Houle, M. M. Taher, K. Valerie, and J. Huot, “Transendothelial migration of colon carcinoma cells requires expression of E-selectin by endothelial cells and activation of stress-activated protein kinase-2 (SAPK2/p38) in the tumor cells,” The Journal of Biological Chemistry, vol. 276, no. 36, pp. 33762–33772, 2001.
View at: Publisher Site | Google Scholar
S. Rousseau, F. Houle, J. Landry, and J. Huot, “p38 MAP kinase activation by vascular endothelial growth factor mediates actin reorganization and cell migration in human endothelial cells,” Oncogene, vol. 15, no. 18, pp. 2169–2177, 1997.
View at: Publisher Site | Google Scholar
Y.-H. Li and C. Zhu, “A modified Boyden chamber assay for tumor cell transendothelial migration in vitro,” Clinical and Experimental Metastasis, vol. 17, no. 5, pp. 423–429, 1999.
View at: Publisher Site | Google Scholar
E. S. Wittchen, R. A. Worthylake, P. Kelly, P. J. Casey, L. A. Quilliam, and K. Burridge, “Rap1 GTPase inhibits leukocyte transmigration by promoting endothelial barrier function,” The Journal of Biological Chemistry, vol. 280, no. 12, pp. 11675–11682, 2005.
View at: Publisher Site | Google Scholar
C. T. Mierke, P. Kollmannsberger, D. Paranhos-Zitterbart, J. Smith, B. Fabry, and W. H. Goldmann, “Mechano-coupling and regulation of contractility by the vinculin tail domain,” Biophysical Journal, vol. 94, no. 2, pp. 661–670, 2008.
View at: Publisher Site | Google Scholar
A. M. P. Montgomery, J. C. Becker, C.-H. Siu et al., “Human neural cell adhesion molecule L1 and rat homologue NILE are ligands for integrin $a_{v} ß_{3}$ ,” The Journal of Cell Biology, vol. 132, no. 3, pp. 475–485, 1996.
View at: Publisher Site | Google Scholar
C. D. Buckley, R. Doyonnas, J. P. Newton et al., “Identification of $a$ v $ß$ 3 as a heterotypic ligand for CD31/PECAM-1,” Journal of Cell Science, vol. 109, no. 2, pp. 437–445, 1996.
View at: Google Scholar
S. Aigner, C. L. Ramos, A. Hafezi-Moghadam et al., “CD24 mediates rolling of breast carcinoma cellson P-selectin,” The FASEB Journal, vol. 12, no. 12, pp. 1241–1251, 1998.
View at: Google Scholar
J. D. Humphries and M. J. Humphries, “CD14 is a ligand for the integrin $α$ 4 $β$ 1,” FEBS Letters, vol. 581, no. 4, pp. 757–763, 2007.
View at: Publisher Site | Google Scholar
W.-J. Lee, W.-K. Chen, C.-J. Wang, W.-L. Lin, and T.-H. Tseng, “Apigenin inhibits HGF-promoted invasive growth and metastasis involving blocking PI3K/Akt pathway and $β$ 4 integrin function in MDA-MB-231 breast cancer cells,” Toxicology and Applied Pharmacology, vol. 226, no. 2, pp. 178–191, 2008.
View at: Publisher Site | Google Scholar
M. R. Morgan, G. J. Thomas, A. Russell, I. R. Hart, and J. F. Marshall, “The integrin cytoplasmic-tail motif EKQKVDLSTDC is sufficient to promote tumor cell invasion mediated by matrix metalloproteinase (MMP)-2 or MMP-9,” The Journal of Biological Chemistry, vol. 279, no. 25, pp. 26533–26539, 2004.
View at: Publisher Site | Google Scholar
U. M. Chandrasekharan, M. Siemionow, M. Unsal et al., “Tumor necrosis factor $a$ (TNF- $a$ ) receptor-II is required for TNF- $a$ -induced leukocyte-endothelial interaction in vivo,” Blood, vol. 109, no. 5, pp. 1938–1944, 2007.
View at: Publisher Site | Google Scholar
H. M. McGettrick, J. M. Lord, K.-Q. Wang, G. E. Rainger, C. D. Buckley, and G. B. Nash, “Chemokine- and adhesion-dependent survival of neutrophils after transmigration through cytokine-stimulated endothelium,” Journal of Leukocyte Biology, vol. 79, no. 4, pp. 779–788, 2006.
View at: Publisher Site | Google Scholar
W. M. Gallatin, I. L. Weissman, and E. C. Butcher, “A cell-surface molecule involved in organ-specific homing of lymphocytes,” Nature, vol. 304, no. 5921, pp. 30–34, 1983.
View at: Publisher Site | Google Scholar
P. Hillyer, E. Mordelet, G. Flynn, and D. Male, “Chemokines, chemokine receptors and adhesion molecules on different human endothelia: discriminating the tissue-specific functions that affect leucocyte migration,” Clinical and Experimental Immunology, vol. 134, no. 3, pp. 431–441, 2003.
View at: Publisher Site | Google Scholar
J. Reiland, L. T. Furcht, and J. B. McCarthy, “CXC-chemokines stimulate invasion and chemotaxis in prostate carcinoma cells through the CXCR2 receptor,” Prostate, vol. 41, no. 2, pp. 78–88, 1999.
View at: Publisher Site | Google Scholar
H. Chopra, S. E. Fligiel, J. S. Hatfield et al., “An in vivo study of the role of the tumor cell cytoskeleton in tumor cell-platelet-endothelial cell interactions,” Cancer Research, vol. 50, no. 23, pp. 7686–7696, 1990.
View at: Google Scholar
A. Janowska-Wieczorek, L. A. Marquez-Curtis, M. Wysoczynski, and M. Z. Ratajczak, “Enhancing effect of platelet-derived microvesicles on the invasive potential of breast cancer cells,” Transfusion, vol. 46, no. 7, pp. 1199–1209, 2006.
View at: Publisher Site | Google Scholar
A. Janowska-Wieczorek, M. Wysoczynski, J. Kijowski et al., “Microvesicles derived from activated platelets induce metastasis and angiogenesis in lung cancer,” International Journal of Cancer, vol. 113, no. 5, pp. 752–760, 2005.
View at: Publisher Site | Google Scholar
C. T. Mierke, M. Ballmaier, U. Werner, M. P. Manns, K. Welte, and S. C. Bischoff, “Human endothelial cells regulate survival and proliferation of human mast cells,” Journal of Experimental Medicine, vol. 192, no. 6, pp. 801–811, 2000.
View at: Publisher Site | Google Scholar
N. Nonomura, H. Takayama, K. Nishimura et al., “Decreased number of mast cells infiltrating into needle biopsy specimens leads to a better prognosis of prostate cancer,” British Journal of Cancer, vol. 97, no. 7, pp. 952–956, 2007.
View at: Publisher Site | Google Scholar
M. F. Acikalin, Ü. Öner, I. Topçu, B. Yaşar, H. Kiper, and E. Çolak, “Tumour angiogenesis and mast cell density in the prognostic assessment of colorectal carcinomas,” Digestive and Liver Disease, vol. 37, no. 3, pp. 162–169, 2005.
View at: Publisher Site | Google Scholar
H. J. Nielsen, U. Hansen, I. J. Christensen, C. M. Reimert, N. Brünner, and F. Moesgaard, “Independent prognostic value of eosinophil and mast cell infiltration in colorectal cancer tissue,” Journal of Pathology, vol. 189, no. 4, pp. 487–495, 1999.
View at: Publisher Site | Google Scholar
J. B. Wyckoff, Y. Wang, E. Y. Lin et al., “Direct visualization of macrophage-assisted tumor cell intravasation in mammary tumors,” Cancer Research, vol. 67, no. 6, pp. 2649–2656, 2007.
View at: Publisher Site | Google Scholar
M. Yang, L. Li, P. Jiang, A. R. Moossa, S. Penman, and R. M. Hoffman, “Dual-color fluorescence imaging distinguishes tumor cells from induced host angiogenic vessels and stromal cells,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 24, pp. 14259–14262, 2003.
View at: Publisher Site | Google Scholar
R. M. Hoffman and M. Yang, “Color-coded fluorescence imaging of tumor-host interactions,” Nature Protocols, vol. 1, no. 2, pp. 928–935, 2006.
View at: Publisher Site | Google Scholar
A. K. Harris, P. Wild, and D. Stopak, “Silicone rubber substrata: a new wrinkle in the study of cell locomotion,” Science, vol. 208, no. 4440, pp. 177–179, 1980.
View at: Publisher Site | Google Scholar
R. J. Pelham Jr. and Y.-L. Wang, “Cell locomotion and focal adhesions are regulated by substrate flexibility,” Proceedings of the National Academy of Sciences of the United States of America, vol. 94, no. 25, pp. 13661–13665, 1997.
View at: Publisher Site | Google Scholar
M. Dembo and Y.-L. Wang, “Stresses at the cell-to-substrate interface during locomotion of fibroblasts,” Biophysical Journal, vol. 76, no. 4, pp. 2307–2316, 1999.
View at: Publisher Site | Google Scholar
J. P. Butler, I. M. Toli-Nørrelykke, B. Fabry, and J. J. Fredberg, “Traction fields, moments, and strain energy that cells exert on their surroundings,” American Journal of Physiology, vol. 282, no. 3, pp. C595–C605, 2002.
View at: Google Scholar
B. Sabass, M. L. Gardel, C. M. Waterman, and U. S. Schwarz, “High resolution traction force microscopy based on experimental and computational advances,” Biophysical Journal, vol. 94, no. 1, pp. 207–220, 2008.
View at: Publisher Site | Google Scholar
C. Raupach, D. P. Zitterbart, C. T. Mierke, C. Metzner, F. A. Müller, and B. Fabry, “Stress fluctuations and motion of cytoskeletal-bound markers,” Physical Review E, vol. 76, Article ID 011918, 12 pages, 2007.
View at: Publisher Site | Google Scholar
P. Jones, P. Jackson, G. J. Price et al., “Identification of a talin binding site in the cytoskeletal protein vinculin,” The Journal of Cell Biology, vol. 109, no. 6, pp. 2917–2927, 1989.
View at: Publisher Site | Google Scholar
R. P. Johnson and S. W. Craig, “An intramolecular association between the head and tail domains of vinculin modulates talin binding,” The Journal of Biological Chemistry, vol. 269, no. 17, pp. 12611–12619, 1994.
View at: Google Scholar
W. H. Goldmann, M. Schindl, T. J. Cardozo, and R. M. Ezzell, “Motility of vinculin-deficient F9 embryonic carcinoma cells analyzed by video, laser confocal, and reflection interference contrast microscopy,” Experimental Cell Research, vol. 221, no. 2, pp. 311–319, 1995.
View at: Publisher Site | Google Scholar
C. E. Turner, “Paxillin and focal adhesion signalling,” Nature Cell Biology, vol. 2, no. 12, pp. E231–E236, 2000.
View at: Publisher Site | Google Scholar
D. R. Critchley, “Focal adhesions—the cytoskeletal connection,” Current Opinion in Cell Biology, vol. 12, no. 1, pp. 133–139, 2000.
View at: Publisher Site | Google Scholar
J.-L. Coll, A. Ben-Ze'ev, R. M. Ezzell et al., “Targeted disruption of vinculin genes in F9 and embryonic stem cells changes cell morphology, adhesion, and locomotion,” Proceedings of the National Academy of Sciences of the United States of America, vol. 92, no. 20, pp. 9161–9165, 1995.
View at: Publisher Site | Google Scholar
R. M. Saunders, M. R. Holt, L. Jennings et al., “Role of vinculin in regulating focal adhesion turnover,” European Journal of Cell Biology, vol. 85, no. 6, pp. 487–500, 2006.
View at: Publisher Site | Google Scholar
W. Xu, H. Baribault, and E. D. Adamson, “Vinculin knockout results in heart and brain defects during embryonic development,” Development, vol. 125, no. 2, pp. 327–337, 1998.
View at: Google Scholar
M. C. Subauste, O. Pertz, E. D. Adamson, C. E. Turner, S. Junger, and K. M. Hahn, “Vinculin modulation of paxillin-FAK interactions regulates ERK to control survival and motility,” The Journal of Cell Biology, vol. 165, no. 3, pp. 371–381, 2004.
View at: Publisher Site | Google Scholar
C. T. Mierke, P. Kollmannsberger, D. Paranhos-Zitterbart et al., “Vinculin contributes to cell invasion by regulating contractile force activation,” 2009.
View at: Google Scholar
J. Guck, S. Schinkinger, B. Lincoln et al., “Optical deformability as an inherent cell marker for testing malignant transformation and metastatic competence,” Biophysical Journal, vol. 88, no. 5, pp. 3689–3698, 2005.
View at: Publisher Site | Google Scholar
X. Fu, J. M. Besterman, A. Monosov, and R. M. Hoffman, “Models of human metastatic colon cancer in nude mice orthotopically constructed by using histologically intact patient specimens,” Proceedings of the National Academy of Sciences of the United States of America, vol. 88, no. 20, pp. 9345–9349, 1991.
View at: Publisher Site | Google Scholar
T. Furukawa, X. Fu, T. Kubota, M. Watanabe, M. Kitajima, and R. M. Hoffman, “Nude mouse metastatic models of human stomach cancer constructed using orthotopic implantation of histologically intact tissue,” Cancer Research, vol. 53, no. 5, pp. 1204–1208, 1993.
View at: Google Scholar
Y. Amoh, M. Yang, L. Li et al., “Nestin-linked green fluorescent protein transgenic nude mouse for imaging human tumor angiogenesis,” Cancer Research, vol. 65, no. 12, pp. 5352–5357, 2005.
View at: Publisher Site | Google Scholar

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Copyright © 2008 Claudia Tanja Mierke. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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