- Primary research
- Open Access
Comparison of angiogenesis-related factor expression in primary tumor cultures under normal and hypoxic growth conditions
© Heinzman et al; licensee BioMed Central Ltd. 2008
Received: 18 January 2008
Accepted: 10 July 2008
Published: 10 July 2008
A localized hypoxic environment occurs during tumor growth necessitating an angiogenic response or tumor necrosis results. Novel cancer treatment strategies take advantage of tumor-induced vascularisation by combining standard chemotherapeutic agents with angiogenesis-inhibiting agents. This has extended the progression-free interval and prolonged survival in patients with various types of cancer. We postulated that the expression levels of angiogenesis-related proteins from various primary tumor cultures would be greater under hypoxic conditions than under normoxia.
Fifty cell sources, including both immortalized cell lines and primary carcinoma cells, were incubated under normoxic conditions for 48 hours. Then, cells were either transferred to a hypoxic environment (1% O2) or maintained at normoxic conditions for an additional 48 hours. Cell culture media from both conditions was collected and analyzed via an ELISA-based assay to determine expression levels of 11 angiogenesis-related factors: VEGF, PDGF-AA, PDGF-AA/BB, IL-8, bFGF/FGF-2, EGF, IP-10/CXCL10, Flt-3 ligand, TGF-β1, TGF-β2, and TGF-β3.
A linear correlation between normoxic and hypoxic growth conditions exists for expression levels of eight of eleven angiogenesis-related proteins tested including: VEGF, IL-8, PDGF-AA, PDGF-AA/BB, TGF-β1, TGF-β2, EGF, and IP-10. For VEGF, the target of current therapies, this correlation between hypoxia and higher cytokine levels was greater in primary breast and lung carcinoma cells than in ovarian carcinoma cells or tumor cell lines. Of interest, patient cell isolates differed in the precise pattern of elevated cytokines.
As linear correlations exist between expression levels of angiogenic factors under normoxic and hypoxic conditions in vitro, we propose that explanted primary cells may be used to probe the in vivo hypoxic environment. Furthermore, differential expression levels for each sample across all proteins examined suggests it may be possible to build a predictor for angiogenesis-related anticancer agents, as each sample has a unique expression profile. Further studies should be performed to correlate in vitro protein expression levels of angiogenesis-related factors with in vivo patient response.
As a tumor grows, the existing blood supply becomes inefficient at supporting the tissue, and areas of the tumor become hypoxic. The hypoxic condition triggers the tumor to enhance the expression of angiogenic factors, triggering the formation of new blood vessels to support the growing tissue [1, 2]. Angiogenesis is required for tumor survival as well as further growth, progression and metastasis . In fact, high tumor vascular density is correlated with negative patient outcomes, including shorter progression-free interval and reduced overall survival [1, 4, 5].
One angiogenic factor whose expression is induced in response to a hypoxic environment is vascular endothelial growth factor (VEGF). VEGF belongs to the cystine-knot family of growth factors . Four homologous polypeptides for VEGF exist, derived by alternative splicing of mRNA . VEGF is secreted by cancer cells as well as supporting stromal cells, including fibroblasts, especially during conditions of hypoxia . In vitro studies have shown that stromal cells cultured in hypoxic growth conditions secrete higher levels of critical angiogenesis-inducing factors than cells cultured in normoxic conditions . High expression of VEGF is observed in many tumor types and is correlated with aggressive tumor growth and metastasis [5–7].
Regulation of VEGF is complex, occurring at both the transcription and translation stages of protein synthesis, with many ligand-receptor interactions [2, 3, 8]. Expression of VEGF is up-regulated by hypoxia inducible factor-1 (HIF-1), which binds to the VEGF promoter, increasing transcription of VEGF [9, 10]. Once expressed, VEGF has the ability to bind to two endothelial cell-specific receptors, kinase domain receptor (KDR, VEGFR2) and fms-like tyrosine kinase (Flt-1, VEGFR1) to initiate angiogenesis among other survival signals [4, 11]. While VEGF binds to Flt-1 with 50-fold higher affinity, KDR binding is more important for angiogenic responses . Brogi et al. found hypoxia induced a 13-fold increase in the number of KDR receptors per endothelial cell in vitro, which may be the mechanism of action for the pronounced effect of hypoxia and VEGF in vivo . In addition to simulating endothelial cell proliferation and migration, VEGF increases vasculature permeability, earning its other name as vascular permeability factor (VPF) [8, 10, 13]. This vascular leakage is critical for initiating angiogenesis as it allows proteins, such as matrix metalloproteases (MMPs), to be deposited in the extracellular fluid . MMPs break down the extracellular matrix to enable endothelial cells to migrate and invade areas in close proximity to the tumor .
Description and role of angiogenesis-related factors.
Role in Angiogenesis
Vascular Endothelial Growth Factor/Vascular Permeability Factor
Signalling protein for angiogenesis that works by binding, dimerizing, and phosphorylating external tyrosine kinase receptors. Can be induced by hypoxia through the release of Hypoxia Inducible Factor (HIF) [4, 6, 8, 10, 13].
Basic Fibroblast Growth Factor
Epidermal Growth Factor
Factor commonly expressed in carcinomas involved in tumor growth, proliferation, and differentiation by stimulation of intrinsic protein-tyrosine kinase activity, resulting in DNA synthesis. Also, induces VEGF, IL-8, and bFGF release by tumor cells [9, 19].
Fms-related Tyrosine Kinase
Cytokine that assists in proliferation and maturation of hematopoietic progenitor cells .
Platelet-derived Growth Factors
Interferon-gamma-inducible Protein 10
Inhibits tumor growth by regulating lymphocyte chemotaxis and inhibiting endothelial cell growth. Down-regulation correlated with poor prognosis. Reverse-correlated with VEGF .
Transforming Growth Factors
Cytokines that control several biological processes including cell growth, proliferation, differentiation, and apoptosis. Pathological conditions such as cancer are can be linked to modifications of these growth factors .
VEGF production by tumor cells is of particular interest as this growth factor is being targeted by new anticancer agents. Specifically, Bevacizumab (Avastin®, Genentech) is a recombinant humanized monoclonal antibody, approved for the treatment of colorectal cancer and non-small cell lung cancer treatment by the FDA [5, 7, 22]. This drug binds VEGF with high specificity, neutralizing the growth factor and preventing the interaction of VEGF with its receptors. Therefore, proliferation of endothelial cells is inhibited and tumor progression is hindered [8, 11].
Based on physiological in vivo conditions, it was hypothesized that cells grown in a hypoxic in vitro environment will express angiogenic factors, including VEGF, at higher levels than those grown under normoxic conditions. A secondary goal of this study was to determine whether primary tumors exhibit differential expression of angiogenic-related factors, a phenomenon which may be useful in predicting patient response to anti-angiogenic anticancer agents.
Primary cell cultures
Primary cell cultures were established using tumor specimens procured for research purposes from the following sources: National Disease Research Interchange (NDRI) (Philadelphia, PA), Cooperative Human Tissue Network (CHTN) (Philadelphia, PA), Forbes Regional Hospital (Monroeville, PA), Jameson Hospital (New Castle, PA), Saint Barnabas Medical Center (Livingston, NJ), Hamot Medical Center (Erie, PA), and Windber Research Institute (Windber, PA). Upon receipt, all specimens were minced to a fine consistency with Cincinnati Surgical #10 or #11 scalpels (PGC Scientifics, Frederick, MD), followed by antibiotic washes, as necessary. In order to establish primary cultures, the specimens were typically divided into 25 cm2 and/or 75 cm2 Cellstar® sterile tissue culture flasks with filtered caps (PGC Scientifics, Frederick, MD), depending on the desired seeding density. Cell culture media were tumor type specific: breast tumors were cultured in Mammary Epithelial Growth Media (MEGM; Lonza Bio Science Walkersville, Walkersville, MD), ovarian tumors were cultured in McCoy's 5A growth media (Mediatech, Herndon, VA), lung tumors were cultured in Bronchial Epithelial Growth Media (BEGM; Lonza Bio Science Walkersville), and colon tumors were cultured in RPMI 1640 growth media (Mediatech). The amount of Fetal Bovine Serum (FBS; HyClone, Logan, UT) present in the media was also tumor-type specific, as was the presence of PureCol™ collagen (Inamed Biomaterials, Fremont, CA) on the culture surface. Antibiotic washes and antibiotic media were formulated with Penicillin-Streptomycin Solution (Mediatech), Gibco Gentamicin Reagent Solution (Invitrogen Corporation, Grand Island, NY), Fungisone (Invitrogen), Cipro® I.V. (ciprofloxacin) (Oncology Therapeutics Network, South San Francisco, CA), and Nystatin (Sigma-Aldrich, St. Louis, MO). Other reagents include Trypsin EDTA (0.25%) and Hanks Buffered Saline Solution with and without Calcium and Magnesium (HBSS) (Mediatech).
All cultures were initially established in humidified incubators at 37°C with 5% CO2 for 5 to 28 days. When a confluency of at least 30 percent was attained, cells were trypsinized, counted, and plated as described below.
Established cell lines
Three human tumor-derived immortalized cell lines were also tested in this study: SK-OV-3, ovarian adenocarcinoma; MDA-MB-231, mammary adenocarcinoma; and A549, lung carcinoma (American Type Culture Collection, Manassas, VA). These cell lines were seeded at 50,000 cells per 5 ml in T25 flasks and allowed to grow for one week to approximately 90% confluency. At that time, the cells were trypsinized, counted, and plated as described below.
After the initial culture period, a total of fifty samples (45 primary cultures and 5 cell line samples) were trypsinized, counted, and suspended in culture media to a concentration of 40,000 cells/ml. SK-OV-3 was tested on three separate occasions to ensure consistency of results. Each of the samples was plated at 20,000 cells/well into one well of two separate Greiner 24-well culture plates (CLP Molecular Biology, San Diego, CA). Both plates were maintained under normoxic conditions (5% CO2 and 21% O2) for 48 hours to allow for cell adherence and equilibration. After 48 hours, one plate remained in normoxic conditions while the other plate was transferred to a NAPCO Series 8000WJ Water Jacketed CO2 Incubator (ThermoFisher Scientific, Waltham, MA) where hypoxic conditions were established. Nitrogen gas was injected to purge the incubator of oxygen resulting in a final O2 concentration of 1% while the CO2 concentration was maintained at 5%, as described by Mukherjee et al. . Plates were incubated for an additional 48 hours. At the end of the incubation period, the confluency for each sample was recorded and the supernatant was collected and stored at -80°C. Confluency is the percentage of substrate with adherent cell growth, determined subjectively by a trained technician.
Collected supernatants were sent to Millipore Corporation (Temecula, CA) for protein evaluation via the Beadlyte® CytokineProfiler™ Testing Service, an ELISA-based assay. Evaluated angiogenesis-related cytokines and growth factors included: VEGF, PDGF-AA, PDGF-AA/BB, IL-8, bFGF, EGF, IP-10, Flt-3 ligand, TGF-β1, TGF-β2, and TGF-β3. Additionally, RANTES (Regulated upon Activation, Normal T-cell Expressed, and Secreted), an analyte not related to angiogenesis, was tested as a negative control for a subset of samples . For each analyte, two replicates were performed using 40 μl of supernatant per replicate.
For each analyte, protein expression levels in the normoxic and hypoxic conditions of all samples were combined into a scatter plot. Then, a linear regression of the curve fit for protein concentration under the hypoxic versus normoxic condition was generated for each analyte tested. For all linear regressions, y = mx+b, y is the concentration produced in the hypoxic environment and x is the concentration produced in the normoxic condition. From this regression, the slope, intercept, and correlation of determination (r2) were calculated. The strength of each linear relationship was determined by the r2 value of the linear regression, with r2 values greater than 0.8 considered strong relationships, and r2 values between 0.6 and 0.8 considered moderate relationships. The same parameters were used to assess VEGF expression levels by tumor type. Lastly, comparisons were generated between the eleven angiogenesis-related factors studied for every cell source. The differences between the protein expression levels under the hypoxic condition versus the normoxic condition were calculated. This value was standardized on a scale of zero to one, with zero set equal to the lowest value observed and one set equal to the highest value observed. These values were graphed as a heat map for all samples across all factors. Additionally, Pearson correlation coefficients were calculated for each factor in relation to VEGF expression using the standardized differences between the hypoxic and normoxic expression levels.
Patient specimens and cell lines
Hypoxia-induced expression of angiogenesis-related factors
Linear correlations between normoxic and hypoxic growth conditions of angiogenesis-related factors.
95% CI Slope (m)
95% CI y-
0.9049 to 1.443
98.99 to 1005
-0.06828 to 0.2309
50.21 to 114.5
0.9076 to 1.018
2.366 to 1136
0.8266 to 1.073
-357.1 to 217.1
0.7925 to 0.8720
-20.92 to 17.21
0.8348 to 1.196
-102.7 to 110.1
0.7738 to 0.9817
-292.3 to 237.1
0.4914 to 0.7458
93.33 to 296.1
0.8808 to 1.045
-226.8 to 272.1
-0.1484 to 0.6350
10.64 to 36.07
Hypoxia-induced expression of VEGF is tissue-type dependent
Linear correlations of VEGF between normoxic and hypoxic conditions.
95% CI Slope
95% CI y-
0.8360 to 1.795
-262.5 to 674.7
0.9280 to 1.458
-422.0 to 778.3
-0.3679 to 1.654
58.40 to 2858
0.9049 to 1.443
98.99 to 1005
Differential expression of angiogenesis-related factors across patient samples
This study addressed a number of topics related to the expression of angiogenesis-related factors in normoxic versus hypoxic environments. Specifically, (1) linear correlations exist for a number of angiogenesis-related factors, (2) linear correlations for VEGF exist and group by tumor type, and (3) primary expression levels vary between samples and across factors.
Linear correlations between protein expression in normoxic and hypoxic environments exist for eight of the eleven angiogenesis-related factors tested in this study (Table 2). Hypoxic expression levels were generally higher than normoxic for IL-8 (r2 > 0.95) and VEGF (r2 > 0.60), though only modestly. Both of these factors are expressed to induce vascular growth due to hypoxia in vivo, and appear to do the same in vitro. The degree of difference was surprising, as both IL-8 and VEGF have been reported to be up-regulated in response to hypoxic conditions. IL-8 regulates angiogenesis by promoting survival of endothelial cells, stimulating matrix metalloproteinases, and increasing endothelial permeability [15, 16]. VEGF is a major signalling protein for angiogenesis secreted in higher levels when cells experience hypoxia . IP-10, an anti-angiogenic factor, had lower expression levels in the hypoxic condition than in the normoxic condition (r2 > 0.80). This was expected, as this protein inhibits tumor growth by regulating lymphocyte chemotaxis and inhibiting endothelial growth .
Trends in the expression levels of other growth factors were variable. Lower expression levels were observed in the hypoxic condition for PDGF-AA (r2 > 0.95) and similar levels were observed for PDGF-AA/BB (r2 > 0.80). These results are not surprising as platelet populations are minimal in culture. These cells are non-adherent to flask surfaces and are rinsed away during routine media changes. Different results were observed for each of the transforming growth factors, likely related to the specific role each plays in cancer pathogenesis . Lower expression levels were observed in the hypoxic condition for TGF-β1, while similar expression levels were observed in both conditions for TGF-β2 (r2 > 0.80) and no correlation existed for TGF-β3 (r2 < 0.25). Similar expression levels were observed in both conditions for EGF, which may be due to the fact that EGF induces VEGF, IL-8, and bFGF release by tumor cells, and is transformed in the process . A correlation did not exist for bFGF, which mediates VEGF production and induces extracellular matrix formation. Another in vitro study showed bFGF was unaffected by hypoxia in cell lines . In all, the correlations between the conditions in vitro suggest the expression levels may be linked to in vivo expression of each angiogenesis-related factor, whether measured in normoxic or hypoxic conditions.
The combined results of all cell sources analyzed for VEGF showed a moderate correlation between normoxic and hypoxic expression levels. Stronger linear correlations were observed for breast and lung samples specifically. Breast and lung samples are cultured in unique culture media as compared to ovarian, CNS, and colon samples. Primary breast tumors are cultured in Mammary Epithelial Growth Media (MEGM), while lung tumors are cultured in Bronchial Epithelial Growth Media (BEGM). These media require addition of SingleQuots® to basal media that include EGF. Significantly, EGF induces VEGF, IL-8, and bFGF release by tumor cells . While this SingleQuots® may have contributed to the VEGF production in these tumor types, the other analytes (IL-8 and bFGF) induced by EGF did not correlate by tumor type (data not shown). Therefore, culture media is probably not responsible for the differential expression levels of the ten evaluable angiogenesis-related proteins and a unique fingerprint for each sample. In general, these data suggest in vitro expression levels of VEGF can be measured in either a normoxic or a hypoxic condition, since a linear correlation exists between expression levels in both conditions.
Differential protein expression levels existed for each factor tested in this study, as is evident in Figure 3. In vitro studies show differential degrees of primary tumor response to chemotherapy agents. These response rates correlate with progression-free interval in ovarian cancer patients, which indicates in vitro tests performed on primary cultures may be used to enhance the probability of choosing the best treatment regimen for the patient . Similarly, differential protein expression levels were observed across patients in this study for each of the factors. This suggests it may be possible to build a predictor for angiogenesis-related anticancer agents using an array of protein expression levels observed in vitro.
There are limits to the application of these in vitro results to the in vivo condition. The tumor microenvironment in vivo is unique both in its three-dimensional structure and the chemical environment . This affects cellular behaviour, including response to chemotherapeutic agents. Some researchers have successfully developed culture systems that replicate this three-dimensional interaction of cells . This study, however, employed a monolayer culture system specifically designed to enrich the population of malignant epithelial cells . While toxicity, delivery, metabolism, and clearance affect patient response to therapeutics in vivo, in vitro studies are commonly used in initial testing of novel treatments and have clinical potential when applied .
Although extreme hypoxic conditions may compromise the health of the cells and lead to cell death, similar confluencies between the normoxic and hypoxic condition at the conclusion of testing suggest that the 48 hour incubation prior to testing was sufficient for cell adherence and equilibration (Figure 1). To support this observation, Pilch et al. found that hypoxia did not cause cell death/decreased confluency, as dead cells were not observed in supernatant post-hypoxia . Furthermore, the hypoxic oxygen concentration used in the study in vitro is similar to that reported by Hockel and Vaupel, 2001, in the core of solid tumors in vivo .
Also, in addition to the 11 angiogenesis-related analytes chosen for testing, a negative control unrelated to angiogenesis was also assessed. A chemotactic cytokine, RANTES, is responsible for recruiting leukocytes and activating natural killer cells . This cytokine was not expected to vary in a normoxic versus hypoxic environment, and we found similar expression levels of RANTES for both conditions validating our technical approach.
Multiple techniques are available to assess VEGF expression. Some laboratories employ immunohistochemical (IHC) analysis to determine VEGF receptor levels , usually for diagnostic and prognostic purposes. However, this study employed the Beadlyte® CytokineProfiler™ Testing Service for two reasons. First, this service provides quantitative analysis of the expression levels of the angiogenesis-related factors, including VEGF. Second, testing was performed on malignant epithelial cell cultures, rather than tissue sections. Intact tissue sections that contain tumor cells as well as support tissue and vasculature are generally stained using IHC. VEGF receptors on endothelial cells and monocytes fluoresce. The described culture process selects specifically for malignant epithelial cells . Endothelial cells are selected against by culture conditions, as the media employed do not promote the growth of these cells; monocytes are non-adherent, so are rinsed away in routine media changes . Neither of these cell types is present in the described samples so IHC of the VEGF receptors was not possible.
VEGF production was of most interest to this study due to its role in the mechanism of action of bevacizumab. The testing conditions were optimized to ensure that VEGF production was measurable, so VEGF results were available for all samples tested. Table 3 includes the summary of all data in the "All Samples" field, a total of 50 samples. Results for the other ten analytes had detection levels out of range of the standard curve for at least two samples, if not more. As a result, the sample size for most of these angiogenesis-related factors was less than 50 (Table 2). However, nine of these ten factors had at least 20 samples available for analysis, and were considered evaluable in the study.
As with any anticancer therapeutic agent, there is clinical ambiguity regarding individual patient response. Some agents directly target VEGF, such as bevacizumab, a humanized monoclonal antibody, while others indirectly target receptors and downstream regulators, such as sunitinib and rituximab . While the regulation and metabolism are unique in vivo, the protein expression levels produced by individual patient cells may provide information on how each patient will respond clinically to a given anticancer agent. The heterogeneity of protein expression demonstrated in this study may provide information to enable the prediction of the efficacy of anti-angiogenic factors. Further studies correlating the in vitro expression levels with patient outcome are warranted.
Linear correlations exist between expression levels of angiogenesis-related factors under normoxic and hypoxic conditions. This suggests the behaviour of primary cells derived from patient tumors grown under in vitro normoxic conditions may provide a correlation to the in vivo hypoxic environment. Differential expression for each sample across all factors suggests predictive value for angiogenesis-related anti-cancer agents, using not only VEGF, but an array of angiogenesis-related proteins. These data suggest further studies should be considered to correlate in vitro expression of these proteins with in vivo patient response to anti-angiogenesis therapeutics.
We thank Dr. David Peters for his data analysis guidance and assistance with the generation of figures. Mr. David Gingrich is thanked for providing statistical analyses and insights.
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