Blood vessel hyperpermeability and pathophysiology in human tumour xenograft models of breast cancer: a comparison of ectopic and orthotopic tumours
© Ho et al.; licensee BioMed Central Ltd. 2012
Received: 21 June 2012
Accepted: 12 November 2012
Published: 5 December 2012
Human tumour xenografts in immune compromised mice are widely used as cancer models because they are easy to reproduce and simple to use in a variety of pre-clinical assessments. Developments in nanomedicine have led to the use of tumour xenografts in testing nanoscale delivery devices, such as nanoparticles and polymer-drug conjugates, for targeting and efficacy via the enhanced permeability and retention (EPR) effect. For these results to be meaningful, the hyperpermeable vasculature and reduced lymphatic drainage associated with tumour pathophysiology must be replicated in the model. In pre-clinical breast cancer xenograft models, cells are commonly introduced via injection either orthotopically (mammary fat pad, MFP) or ectopically (subcutaneous, SC), and the organ environment experienced by the tumour cells has been shown to influence their behaviour.
To evaluate xenograft models of breast cancer in the context of EPR, both orthotopic MFP and ectopic SC injections of MDA-MB-231-H2N cells were given to NOD scid gamma (NSG) mice. Animals with matched tumours in two size categories were tested by injection of a high molecular weight dextran as a model nanocarrier. Tumours were collected and sectioned to assess dextran accumulation compared to liver tissue as a positive control. To understand the cellular basis of these observations, tumour sections were also immunostained for endothelial cells, basement membranes, pericytes, and lymphatic vessels.
SC tumours required longer development times to become size matched to MFP tumours, and also presented wide size variability and ulcerated skin lesions 6 weeks after cell injection. The 3 week MFP tumour model demonstrated greater dextran accumulation than the size matched 5 week SC tumour model (for P < 0.10). Immunostaining revealed greater vascular density and thinner basement membranes in the MFP tumour model 3 weeks after cell injection. Both the MFP and SC tumours showed evidence of insufficient lymphatic drainage, as many fluid-filled and collagen IV-lined spaces were observed, which likely contain excess interstitial fluid.
Dextran accumulation and immunostaining results suggest that small MFP tumours best replicate the vascular permeability required to observe the EPR effect in vivo. A more predictable growth profile and the absence of ulcerated skin lesions further point to the MFP model as a strong choice for long term treatment studies that initiate after a target tumour size has been reached.
KeywordsTumour xenograft models Orthotopic transplantation Ectopic transplantation Enhanced permeability and retention Breast cancer Blood vessel hyperpermeability Nanomedicine Targeting
Pre-clinical development of anti-cancer therapeutics relies on availability of relevant and reproducible in vivo tumour models. Human tumour xenograft models in immunodeficient mice are widely used to assess pharmacokinetics, biodistribution, and treatment efficacy because they are inexpensive and easy to replicate . However, their utility in evaluating potential treatment strategies depends on their capacity to recapitulate human disease conditions.
Progress in nanomedicine seeks to shift distribution of therapeutic compounds to tumour tissue by targeting hyperpermeable tumour vasculature [2, 3]. Tumours are restricted in size until they can trigger greater blood vessel density through angiogenesis and blood vessel remodeling [4, 5]. Compared to normal tissue, tumour tissue has been demonstrated to be more permissive to extravasation of macromolecules as a result of abnormal blood vessel structure . Moreover, tumour tissue is subject to poor lymphatic drainage, leading to greater retention of material in the extravascular space. These combined phenomena are called enhanced permeability and retention (EPR) and form the basis for improved selectivity of nanoscale drug delivery for solid tumour targeting [2, 4, 6].
Several pathological features of tumour vasculature lead to its utility in targeting applications. Pathological tumour vessels are dynamic, and can result both from angiogenesis and remodeling of existing vessels [5, 7]. Endothelial cells that comprise tumour blood vessels have poor organization, leading to gaps between cells, multiple endothelial cell layers, and unusual tortuosity and branching [8, 9]. These openings allow unregulated movement of macromolecules and nanoscale carriers across tumour vessel walls and into the surrounding tissue . In response, the associated basement membrane is also often thickened or absent [9, 11]. This apparent dichotomy stems from a dynamic interaction between increased and multilayered collagen deposition in the basement membrane [10, 12–14] and increased expression of matrix metalloproteinases (MMPs) that can result in collagen degradation . Further enhancing the aberrant permeability of tumour blood vessels, the pericytes that normally cover and stabilize the outer vessel wall can also be missing or detached, leading to a more immature vessel structure . The absence of these contractile support cells may lead to further increased vessel permeability and weakened control over blood flow . Lymphatic vessels are closely associated with and derived from the blood vessel network. They are responsible for transporting waste out of tissues, but tumours are often deficient in lymphatic drainage, leading to increased accumulation of macromolecular material in tumour tissue . Each of these features contributes to the pathophysiology that enables the EPR effect. Vascular permeability factors, such as bradykinin and nitric oxide, also mediate and enhance vascular hyperpermeability ; however, our analysis will be limited to physical vascular defects and their contributions to EPR.
To validate the use of human tumour xenografts in mouse models of breast cancer to investigate tumour targeting via EPR, we studied MDA-MB-231-H2N cells transplanted in NOD scid gamma (NSG) mice and compared two common cell injection sites in the context of EPR permissive pathology. Owing to its simplicity, tumour cells are often introduced ectopically as subcutaneous (SC) injections, regardless of their native tissue type [17–19]. Cells injected orthotopically (eg. breast cancer cells into mammary tissue) are subject to biological cues present in the relevant organ environment . Allowing tumour cells to grow in their orthotopic environment influences growth rate, blood and lymphatic vessel development, metastatic potential, interstitial pressure, and response to therapy [5, 18–21]. We hypothesized that the orthotopic environment may also influence the permeability of the resulting tumour vasculature. Notably, to promote successful tumour engraftment in both locations, our chosen cell line is known to be tumourigenic in the absence of external factors, such as estrogen . Groups of animals were compared as cohorts of matching tumour size because size, and not elapsed time, is a standard prognostic measure used to assess breast cancer stage .
Currently, the benefit of using either SC or MFP in xenograft models of breast cancer in assessing targeting through the EPR effect is not well characterized. To investigate vessel permeability, orthotopic and ectopic tumour-bearing NSG mice were given intravenous injections of a fluorescently labeled high molecular weight dextran (FITC-Dextran, 2 MDa, ~80 nm ) as a model nanocarrier. After allowing the dextran to circulate, animals were sacrificed, their tumours removed, measured using calipers, and fixed with paraformaldehyde. Tumours were cryosectioned and examined for dextran accumulation. Tissue sections were also immunostained for markers of vascular endothelial cells (CD31), basement membrane (collagen IV), pericytes (alpha smooth muscle actin (αSMA)), and lymphatic vessels (lymphatic vessel endothelial hyaluronan receptor (LYVE-1)).
All cell culture materials were purchased from Gibco-Invitrogen (Burlington, ON, Canada). MDA-MB-231-H2N cells and NOD scid gamma (NSG) mice were generous gifts from Dr. Robert Kerbel (Sunnybrook Research Institute, Toronto, ON, Canada), which were then maintained or bred in-house. Lysine-fixable dextran-FITC (MW 2 ± 0.2 MDa) was purchased from Invitrogen (Burlington, ON, Canada). Slides and cover slips were purchased from Fisher Scientific (Ottawa, ON, Canada). Primary antibodies were purchased from Abcam (Cambridge, MA, USA) for CD31 (ab28364), LYVE-1 (ab14917), collagen IV (ab19808), and αSMA (ab5694). Immunostaining reagents (rabbit IgG Elite ABC kit, avidin/biotin kit, enzyme substrates, Vectashield mounting medium) were purchased from Vector Labs (Burlington, ON, Canada). Entellan hard mounting medium was purchased from EMD Millipore (Billerica, MA, USA). All other materials were purchased from Sigma-Aldrich (Mississauga, ON, Canada) and used as received unless otherwise noted.
Cell maintenance and preparation
MDA-MB-231-H2N cells were maintained in RPMI 1640 culture medium, supplemented with 10% heat-inactivated fetal bovine serum (FBS), 50 units/mL penicillin and 50 mg/mL streptomycin under a humidified 5% CO2 environment. To prepare cell suspensions for injection, adherent cells were first rinsed with phosphate buffered saline, pH 7.4 (PBS), and then incubated briefly with trypsin-ethylenediamine tetraacetic acid (trypsin-EDTA, 0.25%/0.038%). Once the cells were suspended, enzymatic digestion was inhibited with FBS, and the cells were pelleted and washed 3 times in PBS before resuspension at the desired concentration. Cells were kept on ice prior to injection.
Tumour xenograft models
The protocols used in these in vivo studies were approved by the University Health Network Animal Care Committee and performed in accordance with current institutional and national regulations. Animals were housed in a 12 h light and 12 h dark cycle with free access to food and water. NSG mice were bred in-house, and 7–9 week old female mice were selected for tumour xenotransplantation.
Mice in all experimental groups were inoculated with 106 MDA-MB-231-H2N cells suspended in 50 μL of sterile PBS. Prior to injection, mice were anaesthetized with isoflurane-oxygen. To form ectopic SC tumours, anaesthetized mice were injected with cells under the skin in the right dorsal flank. To form orthotopic mammary fat pad (MFP) tumours, the surgical area was depilated and swabbed with 70% ethanol and betadine before making an incision in the skin of the lower abdomen to the right of the midline, uncovering the mammary fat pad in the right inguinal region where cells were injected into the fat pad. The incision was then sutured closed and lactated Ringer’s solution and buprenorphine were given post-operatively for recovery and pain management. Solid tumours were allowed to form over a period of 3–5 weeks. Cohorts of tumour-bearing animals were divided into two groups to proceed onwards for testing; the first group was tested once their tumours reached an average diameter along the major axis of 7 mm as measured through the skin using calipers, and the second group tested the following week.
Dye injections and tissue collection
Once tumours reached their target size, mice were injected with 0.5 mg of FITC-dextran in 200 μL of PBS via intravenous (IV) tail vein injection . After 1 h, animals were sacrificed by CO2 asphyxiation and tissue samples (tumour and liver) were collected by dissection; tumour samples were directly measured for diameter along both the major and minor axes (L and W) and thickness (H) using calipers (ellipsoid volume calculated as π/6 × L × W × H), and each sample was placed separately in cassettes and submerged in 4% paraformaldehyde for 24 h at 4°C. Tissue samples were then cryoprotected in 30% sucrose in PBS and stored at 4°C. Tissue samples were cryosectioned in 10 μm sections, and pairs of slices 50 μm apart were mounted onto slides, and stored at −80°C. For fluorescence analysis, slides were rehydrated in PBS and coverslipped using Vectashield mounting medium.
Immunostaining protocol details listed by antigen
NGS blocking incubation time
Primary antibody dilution
Secondary antibody incubation time
ABC reagent incubation time
Image acquisition and analysis
All fluorescence images (FITC-dextran) were acquired with a fixed exposure time for each channel using an Olympus BX50 with a UPlanSApo 10×/0.40 objective, Photometrics CoolSNAP HQ2 monochrome camera, and motorized stage (Olympus Canada Inc., Richmond Hill, ON, Canada). Images were tiled together using Metamorph, and analyzed using ImageJ. To compensate for blood remaining in tissue after sacrifice, the blood-associated fluorescence intensity was quantified in hepatic sinusoids in liver tissue slices. Pixels matching this intensity were subtracted from the positive pixel count in the subsequent analysis.
Brightfield images (immunostaining) were acquired using an Aperio ScanScope XT (Aperio, Vista, CA, USA) for whole slide scanning at 20× magnification and analyzed using ImageScope Microvessel Analysis. Statistical significance between groups was first tested with Bartlett’s test for equality of variance (P < 0.05). Where variances were equivalent, one-way ANOVA was applied, followed by a corrected unpaired t-test; differences are denoted by square bracket symbols connecting the differing groups (P < 0.05, unless otherwise noted).
Results and discussion
Orthotopic cell transplantation influences tumour growth rate and size variation
To investigate effects associated with tumour size, 4 animals from each tumour type were randomly selected for dextran injection and tumour resection once the 7 mm major axis diameter was reached, with the remaining animals evaluated the following week. The 7 mm target size was selected to allow adequate vascular pathology to develop, as neovascularization of the tumour is most pronounced over serveral days immediately after a palpable mass (20 mm3) has formed . Notably, the week after this target size was reached, tumour size variability increased in both tumour sites (P < 0.05 by Bartlett’s test of equality of variances). Unexpectedly, several tumours in the SC group at 6 weeks post-cell injection were smaller than those observed the previous week (Figure 1). Additionally, several replicates were of similar size or larger size, resulting in a broad size distribution of the resulting tumours. In this group, 4 out of 6 animals developed hard fibrotic tissue leading to an ulcerated skin lesion by this time (an indication for humane sacrifice). These lesions, which made these animals unsuitable for further study beyond this time, were not observed in any other group. MFP tumours were grown from cells injected directly into the centre of the MFP, surrounding transplanted cells with endogenous support cells and forming a biological barrier against contact with the skin, which may have prevented ulceration. These injected cells also had access to the pre-existing vascular network and biological signaling molecules present in the MFP. Overall, the MFP tumours were more consistent in size than the SC tumours. Given that the cell line (MDA-MB-231-H2N) and mouse strain (NSG) that we selected are well-established as highly permissive to tumour xenografts [22, 26], we expect trends to be similar using other combinations of cells and mice. However, it is possible that other systems will behave differently. Given the large variability in the 6 week SC tumour group, these samples were not further analyzed. Instead, 5 week SC tumours were compared with 3 and 4 week MFP tumours, which were similar in size.
MFP tumours exceed SC tumours in model nanocarrier accumulation
Prior to sacrifice, a high molecular weight FITC-dextran, used as a model nanocarrier, was injected to assess blood vessel permeability. Data were normalized to liver tissue collected as a positive control: liver endothelial cells have natural fenestrations (123 ± 24 nm diameter)  for transfer of substrates from the blood to hepatocytes, making the liver an ideal organ for observing nanocarrier uptake. In mice, blood flow through the liver is also estimated at 23% of cardiac output, making it one of the best perfused organs on a per gram basis .
Elements of tumour vascular pathophysiology observed in tumour models
Separate sections were also co-stained for collagen IV to visualize the thickness of the associated basement membrane. The basement membrane forms a physical barrier that inhibits transport of high molecular weight materials across blood vessel walls [15, 32]. In tumour pathophysiology, opposing phenomena have been observed: the basement membrane can thicken, thin, or even be absent. In the MFP and SC tumour models, the basement membrane was thickened compared to healthy liver blood vessels (Figure 3B). This observation is consistent with the xenografted MDA-MB-231-H2N cell line being poorly invasive like its parental line, MDA-MB-231 . Conversely, a more metastatic cell line is often capable of using MMPs to degrade the basement membrane to enable cell migration through neighbouring blood vessels . The 5 week old SC tumours were observed to have the highest basement membrane thickness, indicating the greatest mass transport barrier against nanocarrier delivery.
CD31 staining also revealed differences in vascular density, with the 3 week old MFP tumours having a significantly greater vessel density than the other groups (Figure 3C). The decrease in vascular density from 3 weeks to 4 weeks in the MFP model suggests that the tumour cell growth may be too rapid for the corresponding new blood vessels to form. The thick basement membranes observed in the tumour tissue may also contribute to this deficiency as the basement membrane must be degraded before vascular branching can occur . Although the 3 week old MFP and 5 week old SC tumours were size matched, the MFP model had greater blood vessel density, which may be attributed to greater vascular density in the MFP. Together these observations suggest that remodeling blood vessels already present in the transplantation site are important in establishing relevant tumour vasculature. The relatively poor vascular density in SC tumours may also explain the poor engraftment after 6 weeks, as a lack of blood flow may inhibit further growth and lead to necrosis.
The mean vascular area was also quantified, giving an indication of the size, and therefore the capacity of the blood vessels present in each tumour type. The vascular area in 3 week old MFP tumours was significantly higher than the 4 week old MFP tumours (Figure 3D), indicating that in addition to decreasing vessel density with increasing tumour size, there is on average a lower capacity for blood in the vessels present. Having a greater density and capacity for blood perfusion enhances the likelihood for delivery of materials to the 3 week old MFP tumours through systemic circulation.
At the same time, all of the evaluated models are likely underperfused as their small size categorizes them as microvasculature . This low overall capacity for blood flow impacts their utility in assessing nanocarrier accumulation via EPR, and likely results in regions of hypoxia and heterogeneous drug distribution.
There is evidence that both the MFP and SC tumour models yielded poor lymphatic drainage compared to healthy tissue. Accumulation of interstitial fluid in cases of lymphedema has been shown to lead to the deposition of collagen . Visual examination of the tumour slices revealed a high density of collagen IV-lined spaces that were CD31 negative, which likely represent fluid-filled cavities in the tumour tissue (Figure 5C-D). These likely contain excess interstitial fluid resulting from a combination of increased vascular permeability and deficient lymphatic drainage.
Taken together, the data gathered through CD31 and collagen IV immunostaining suggest that, of the models tested, the 3 week MFP tumour best replicates the vascular permeability required to observe the EPR effect in vivo. However, the blood vessels visualized are sparse and small, contributing to low accumulation of the model nanocarrier used in this study. Both MFP and SC tumours showed evidence of excess interstitial fluid accumulation, suggesting poor lymphatic drainage in both models. While MFP tumours demonstrated greater lymphatic vessel density, SC tumours had greater lymphatic vessel size, both of which contribute to drainage, making it difficult to easily differentiate the two models in terms of drainage capacity. MFP tumours demonstrated greater utility for long-term treatment studies, as their growth is more consistent at large tumour sizes, and no skin ulcerations were observed.
This study provides insight into the vascular properties of human tumour xenograft models of breast cancer in both MFP (orthotopic) and SC (ectopic) environments, two common pre-clinical models. When both animal models were challenged with a high molecular weight dextran as a model nanocarrier, there was higher accumulation in MFP tumours 3 weeks after cell injection. Further adding to the evidence that MFP tumour vasculature has greater permeability to macromolecules – a pathological feature relevant to nanocarrier accumulation via EPR – CD31 and collagen IV immunostaining revealed greater vascular density and size, as well as thinner basement membranes, in MFP tumours collected 3 weeks after cell injection. Both models demonstrated poor dextran accumulation compared to the liver as a positive control, suggesting that although several pathological features were observed, low vascular density and small blood vessel size led to relatively poor tumour perfusion. Both the MFP and SC tumour models showed evidence of poor lymphatic drainage, as several CD31 negative and collagen IV-lined fluid-filled cavities were observed. The MFP environment offered several practical benefits, including shorter development times to reach a target tumour size, more consistent growth profiles, and the absence of ulcerated skin lesions observed in SC tumour animals.
Alpha smooth muscle actin
Enhanced permeability and retention
Fetal bovine serum
Lymphatic vessel endothelial hyaluronan receptor
Mammary fat pad
Normal goat serum
- NSG mice:
NOD scid gamma mice
Phosphate buffered saline, pH 7.4
We thank: Drs. Robert Kerbel (Sunnybrook Health Science Centre), Armand Keating and Yoko Kosaka (Princess Margaret Hospital) for their help and advice in establishing the mouse tumour model. We are grateful to the Canadian Institutes of Health Research (CIHR to MSS) for funding of this research.
- Teicher BA: Human tumor xenografts and mouse models of human tumors: re-discovering the models. Expert Opin Drug Dis. 2009, 4 (12): 1295-1305. 10.1517/17460440903380430.View Article
- Torchilin V: Tumor delivery of macromolecular drugs based on the EPR effect. Adv Drug Deliver Rev. 2011, 63 (3): 131-135. 10.1016/j.addr.2010.03.011.View Article
- Fang J, Nakamura H, Maeda H: The EPR effect: unique features of tumor blood vessels for drug delivery, factors involved, and limitations and augmentation of the effect. Adv Drug Deliver Rev. 2011, 63 (3): 136-151. 10.1016/j.addr.2010.04.009.View Article
- Carmeliet P, Jain RK: Angiogenesis in cancer and other diseases. Nature. 2000, 407 (6801): 249-257. 10.1038/35025220.View ArticlePubMed
- Kerbel RS: Tumor angiogenesis: past, present and the near future. Carcinogenesis. 2000, 21 (3): 505-515. 10.1093/carcin/21.3.505.View ArticlePubMed
- Matsumura Y, Maeda H: A new concept for macromolecular therapeutics in cancer-chemotherapy - mechanism of tumoritropic accumulation of proteins and the antitumor agent smancs. Cancer Res. 1986, 46 (12): 6387-6392.PubMed
- Morikawa S, Baluk P, Kaidoh T, Haskell A, Jain RK, McDonald DM: Abnormalities in pericytes on blood vessels and endothelial sprouts in tumors. Am J Pathol. 2002, 160 (3): 985-1000. 10.1016/S0002-9440(10)64920-6.PubMed CentralView ArticlePubMed
- Dreher MR, Liu WG, Michelich CR, Dewhirst MW, Yuan F, Chilkoti A: Tumor vascular permeability, accumulation, and penetration of macromolecular drug carriers. J Natl Cancer I. 2006, 98 (5): 335-344. 10.1093/jnci/djj070.View Article
- Jain RK: Normalization of tumor vasculature: an emerging concept in antiangiogenic therapy. Science. 2005, 307 (5706): 58-62. 10.1126/science.1104819.View ArticlePubMed
- Hashizume H, Baluk P, Morikawa S, McLean JW, Thurston G, Roberge S, Jain RK, McDonald DM: Openings between defective endothelial cells explain tumor vessel leakiness. Am J Pathol. 2000, 156 (4): 1363-1380. 10.1016/S0002-9440(10)65006-7.PubMed CentralView ArticlePubMed
- Sorensen AG, Batchelor TT, Zhang WT, Chen PJ, Yeo P, Wang MY, Jennings D, Wen PY, Lahdenranta J, Ancukiewicz M, et al: A "Vascular Normalization Index" as potential mechanistic biomarker to predict survival after a single dose of cediranib in recurrent glioblastoma patients. Cancer Res. 2009, 69 (13): 5296-5300. 10.1158/0008-5472.CAN-09-0814.PubMed CentralView ArticlePubMed
- Hida K, Hida Y, Shindoh M: Understanding tumor endothelial cell abnormalities to develop ideal anti-angiogenic therapies. Cancer Sci. 2008, 99 (3): 459-466. 10.1111/j.1349-7006.2007.00704.x.View ArticlePubMed
- McDonald DM, Baluk P: Significance of blood vessel leakiness in cancer. Cancer Res. 2002, 62 (18): 5381-5385.PubMed
- Baluk P, Morikawa S, Haskell A, Mancuso M, McDonald DM: Abnormalities of basement membrane on blood vessels and endothelial sprouts in tumors. Am J Pathol. 2003, 163 (5): 1801-1815. 10.1016/S0002-9440(10)63540-7.PubMed CentralView ArticlePubMed
- Lu P, Weaver VM, Werb Z: The extracellular matrix: a dynamic niche in cancer progression. J Cell Biol. 2012, 196 (4): 395-406. 10.1083/jcb.201102147.PubMed CentralView ArticlePubMed
- Wu J, Akaike T, Maeda H: Modulation of enhanced vascular permeability in tumors by a bradykinin antagonist, a cyclooxygenase inhibitor, and a nitric oxide scavenger. Cancer Res. 1998, 58 (1): 159-165.PubMed
- Kerbel RS, Cornil I, Theodorescu D: Importance of orthotopic transplantation procedures in assessing the effects of transfected genes on human tumor-growth and metastasis. Cancer Metast Rev. 1991, 10 (3): 201-215. 10.1007/BF00050792.View Article
- Killion JJ, Radinsky R, Fidler IJ: Orthotopic models are necessary to predict therapy of transplantable tumors in mice. Cancer Metast Rev. 1998, 17 (3): 279-284. 10.1023/A:1006140513233.View Article
- Lunt SJ, Kalliomaki TMK, Brown A, Yang VX, Milosevic M, Hill RP: Interstitial fluid pressure, vascularity and metastasis in ectopic, orthotopic and spontaneous tumours. BMC Cancer. 2008, 8: 2-10.1186/1471-2407-8-2.PubMed CentralView ArticlePubMed
- Wilmanns C, Fan D, Obrian CA, Bucana CD, Fidler IJ: Orthotopic and ectopic organ environments differentially influence the sensitivity of murine colon-carcinoma cells to doxorubicin and 5-fluorouracil. Int J Cancer. 1992, 52 (1): 98-104. 10.1002/ijc.2910520118.View ArticlePubMed
- Francia G, Cruz-Munoz W, Man S, Xu P, Kerbel RS: Mouse models of advanced spontaneous metastasis for experimental therapeutics. Nat Rev Cancer. 2011, 11 (2): 135-141. 10.1038/nrc3001.PubMed CentralView ArticlePubMed
- Holliday DL, Speirs V: Choosing the right cell line for breast cancer research. Breast Cancer Res. 2011, 13 (4): 215-10.1186/bcr2889.PubMed CentralView ArticlePubMed
- Edge SB, Compton CC: The American Joint Committee on Cancer: the 7th edition of the AJCC cancer staging manual and the future of TNM. Ann Surg Oncol. 2010, 17 (6): 1471-1474. 10.1245/s10434-010-0985-4.View ArticlePubMed
- Tomayko MM, Reynolds CP: Determination of subcutaneous tumor size in athymic (Nude) mice. Cancer Chemoth Pharm. 1989, 24 (3): 148-154. 10.1007/BF00300234.View Article
- Schiffelers RM, Metselaar JM, Fens MHAM, Janssen APCA, Molema G, Storm G: Liposome-encapsulated prednisolone phosphate inhibits growth of established tumors in mice. Neoplasia. 2005, 7 (2): 118-127. 10.1593/neo.04340.PubMed CentralView ArticlePubMed
- Ito M, Hiramatsu H, Kobayashi K, Suzue K, Kawahata M, Hioki K, Ueyama Y, Koyanagi Y, Sugamura K, Tsuji K, et al: NOD/SCID/gamma(null)(c) mouse: an excellent recipient mouse model for engraftment of human cells. Blood. 2002, 100 (9): 3175-3182. 10.1182/blood-2001-12-0207.View ArticlePubMed
- Cogger VC, McNerney GP, Nyunt T, DeLeve LD, McCourt P, Smedsrod B, Le Couteur DG, Huser TR: Three-dimensional structured illumination microscopy of liver sinusoidal endothelial cell fenestrations. J Struct Biol. 2010, 171 (3): 382-388. 10.1016/j.jsb.2010.06.001.PubMed CentralView ArticlePubMed
- Davies B, Morris T: Physiological parameters in laboratory-animals and humans. Pharmaceut Res. 1993, 10 (7): 1093-1095. 10.1023/A:1018943613122.View Article
- Hori K, Saito S, Takahashi H, Sato H, Maeda H, Sato Y: Tumor-selective blood flow decrease induced by an angiotensin converting enzyme inhibitor, temocapril hydrochloride. Jpn J Cancer Res. 2000, 91 (2): 261-269. 10.1111/j.1349-7006.2000.tb00940.x.View ArticlePubMed
- Chen B, Pogue BW, Zhou XD, O'Hara JA, Solban N, Demidenko E, Hoopes PJ, Hasan T: Effect of tumor host microenvironment on photodynamic therapy in a rat prostate tumor model. Clin Cancer Res. 2005, 11 (2): 720-727.PubMed
- Tong RT, Boucher Y, Kozin SV, Winkler F, Hicklin DJ, Jain RK: Vascular normalization by vascular endothelial growth factor receptor 2 blockade induces a pressure gradient across the vasculature and improves drug penetration in tumors. Cancer Res. 2004, 64 (11): 3731-3736. 10.1158/0008-5472.CAN-04-0074.View ArticlePubMed
- Kong G, Braun RD, Dewhirst MW: Hyperthermia enables tumor-specific nanoparticle delivery: effect of particle size. Cancer Res. 2000, 60 (16): 4440-4445.PubMed
- Abdelkarim M, Vintonenko N, Starzec A, Robles A, Aubert J, Martin M-L, Mourah S, Podgorniak M-P, Rodrigues-Ferreira S, Nahmias C, et al: Invading basement membrane matrix is sufficient for MDA-MB-231 breast cancer cells to develop a stable in vivo metastatic phenotype. PLoS One. 2011, 6 (8): e23334-10.1371/journal.pone.0023334.PubMed CentralView ArticlePubMed
- Perles-Barbacaru AT, van der Sanden BPJ, Farion R, Lahrech H: How stereological analysis of vascular morphology can quantify the blood volume fraction as a marker for tumor vasculature: comparison with magnetic resonance imaging. J Cerebr Blood F Met. 2012, 32 (3): 489-501. 10.1038/jcbfm.2011.151.View Article
- Rockson SG: Diagnosis and management of lymphatic vascular disease. J Am Coll Cardiol. 2008, 52 (10): 799-806. 10.1016/j.jacc.2008.06.005.View ArticlePubMed
- Schneider M, Ny A, Ruiz De Almodovar C, Carmeliet P: A new mouse model to study acquired lymphedema. PLoS Med. 2006, 3 (7): e264-10.1371/journal.pmed.0030264.PubMed CentralView ArticlePubMed
- Szuba A, Rockson SG: Lymphedema: anatomy, physiology and pathogenesis. Vasc Med. 1997, 2 (4): 321-326.View ArticlePubMed
- The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1471-2407/12/579/prepub
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