- Open Access
Short-term anti-vascular endothelial growth factor treatment elicits vasculogenic mimicry formation of tumors to accelerate metastasis
© Yuan et al; licensee BioMed Central Ltd. 2012
- Received: 29 December 2011
- Accepted: 23 February 2012
- Published: 23 February 2012
Antiangiogenic therapy is one of the most significant advances in anticancer treatment. The benefits of antiangiogenic therapies of late-stage cancers have been investigated but are still too limited.
We used an ovarian cancer model to test the effect of short-term bevacizumab treatment on metastasis as measured by bioluminescence. Western blotting and CD34-PAS dual staining were performed to assess hypoxia-inducible transcription factor-1α (HIF-1α) expression and vasculogenic mimicry(VM) formation. Cell viability was examined by a CCK8 assay.
Bevacizumab demonstrated antitumor effects in models of ovarian cancer, but also accelerated metastasis together, with marked hypoxia and VM formation in mice receiving short-term therapy. Bevacizumab treatment did not affect SKOV3 cell viability and the amount of VM in three-dimensional culture.
These results suggest that antiangiogenic therapy may potentially influence the progression of metastatic disease, which has been linked to the hypoxic response and VM formation.
- Antiangiogenic therapies
- Vasculogenic mimicry
Tumors can grow to a maximum diameter of between 1 and 2 mm before their metabolic demands are restricted due to the diffusion limit of oxygen and lack of essential nutrients. To exceed this size or spread to other organs, tumors require an independent blood supply. In the 1970s, Folkman et al was the first to propose the concept of antiangiogenesis as a therapeutic approach to treat solid tumors . Targeting the blood supply by inhibiting the formation of blood vessel will lead to tumor growth arrest. Numerous angiogenesis inhibitors have been therapeutically used in both preclinical and clinical settings . Vascular endothelial growth factor (VEGF) receptor tyrosine kinase inhibitors and a VEGF-neutralizing antibody have been clinically validated to target VEGF or its receptors as an anticancer treatment. However, a number of limitations are observed in current antiangiogenic therapies. Many clinical benefits are short-lived, and enduring clinical responses are rare. While numerous trials have shown an increase in survival after patients are treated with antiangiogenic therapy, the increase for many was only a matter of months . Moreover, single-agent use of antiangiogenesis appears to be insufficient to improve patient survival . While any improvement in overall survival for patients should be regarded as advancement, it is importart to understand why such clinical improvements are sometimes transitory so that new therapies result in more enduring benefits.
One explanation for these limitations is a potential link between antiangiogenic therapy and increased metastasis . In RIP-Tag2 mice treated with the VEGF receptor 2-inhibitor DC101, although tumors were smaller, they showed significantly more invasive and malignant phenotypes, with most showing wide fronts of invasion into urrounding acinar tissues . Rodents treated with an anti-VEGF antibody showing a striking increase in the number and total area of small satellite tumors compared with those that had not received antiangiogenic therapy, and tumor cells often had migrated over long distances [7, 8]. Together, these results suggest that antiangiogenic therapy may influence the progression of metastatic disease. To understand the reasons for these observations and to enable enduring benefits of antiangiogenic therapies, we examined the effect of a VEGF-neutralizing antibody on metastasis in mice after short-term administration. Furthermore, the hypoxic response and vasculogenic mimicry (VM) formation were assessed in this study.
For western blotting and histopathological analyses, a mouse anti-HIF-1α monoclonal antibody was purchased from Novus Biologicals (Littleton, CO, USA), CD34 monoclonal antibody from Abgent (San Diego, CA, USA).
The human ovarian cancer cell line SKOV3 was purchased from the ATCC and transfected with a luciferase-expressing lentivirus containing an independent open-reading frame of GFP. After 72 hours, cells were examined by fluorescence microscopy to confirm infection. Luciferase expression was determined using luciferin and an in vivo imaging system (Xenogen). Cells were maintained in RPMI-1640 medium supplemented with 10% heatinactivated fetal bovine serum (Gibco Invitrogen Corp), and incubated at 37°C in a humidified atmosphere containing 5% CO2.
Matrigel (BD Biosciences) was placed dropwise onto glass coverslips in 12-well culture plates and allowed to polymerize for 30 min at 37°C. SKOV3 cells were then seeded onto the 3D matrix in complete medium.
SKOV3LUC+ cells (1.2 × 106 cells) were directly injected into the tail vein of 6- 8-week-old female nude mice. Forty mice were assigned into four groups(A, B, C and D). Group A was treated with phosphate-buffered saline (PBS) bi-weekly for 3 weeks. Group B was treated with 40 mg/kg bevacizumab bi-weekly for 3 weeks. Group C was treated with 3 mg/kg cisplatin weekly for 3 weeks. Group D was treated with both bevacizumab bi-weekly and cisplatin weekly for 3 weeks. Bevacizumab and cisplatin were administered intraperitoneally. Body weight was measured and recorded weekly. Metastatic disease progression in SKOV3LUC+ tumor-bearing mice was monitored. Before mice were anesthetized with Forane, an aqueous solution of luciferin (150 mg/kg) was intraperitoneally injected at 10 min prior to imaging. Mice were placed into the light-tight chamber of a CCD camera system (Xenogen), and photons emitted from luciferase-expressing cells within mice were quantified for 1 min, using the software program living. Four weeks after initial treatment, all mice were sacrificed to assess the effects of drug treatments. All procedures involving mice complied with the Guide for the Care and Use of Laboratory Animals (National Institutes of Health).
The tissues were homogenized in 0.5 ml Hepes (50 mM, pH 7.5) containing 100 mM NaCl, 1 mM CaCl2, 1 mM dithiothreitol, 1% ethylene glycol-bis(aminoethyl ether)-tetraacetic acid 1% Triton X- 100 and proteinase inhibitors. Protein extracts were kept in ice for 30 min and then centrifuged at 14,000 g at 4°C for 30 min. Protein concentrations were determined using a bicinchoninic acid protein assay reagent kit. Protein samples (20 mg) were mixed with equal volumes of loading buffer (20% glycerol, 4% sodium dodecyl sulfate, and 100 mM Tris-HCl, pH 6.8) and then boiled for 5 min in the presence of β-mercaptoethanol. Proteins were separated in 8% sodium dodecyl sulfate-polyacrylamide gels at 100 V for 2 h and then electrotransferred to nitrocellulose membranes at 270 mA for 2 h. Membranes were blocked with 5% non-fat dry milk in PBS with 0.1% Tween 20 for 1 h at room temperature. Then, membranes were incubated with anti- HIF-1α (1:500) overnight at 4°C and finally with a horseradish peroxidase-conjugated anti-mouse IgG for 1 h at room temperature after washing with TBS containing 0.1% Tween 20. Proteins were visualized by enhanced chemiluminescence reagents after washing. Protein expression was semi-quantified using an image analysis system.
CD34-PAS dual staining
Four micrometer paraffin sections were routinely deparaffinized and dehydrated. First, CD34 immunohistochemical staining was applied to the sections. Endogenous peroxidase activity was blocked with 3% hydrogen peroxide in 50% methanol for 10 min at room temperature. Sections were rehydrated and washed with PBS and then pretreated with citrate buffer (0.01 M citric acid, pH 6.0) for 20 min at 100°C in a microwave oven. Non-specific binding sites were blocked with 2% normal goat serum in PBS for 20 min at 37°C. Sections were then incubated overnight at 4°C with anti-CD34 at a 1:200 dilution. Then, sections were rinsed with PBS and incubated with biotinylated goat anti-mouse IgG for 20 min at 37°C, followed by incubation with 3,3'-diaminobenzidine(DAB) chromogen for 10 min at room temperature. Sections were then rinsed with water for 1 min to stop the DAB-staining reaction. Formalin and melanin granules were then removed using the methods mentioned above. Finally, sections were treated with 0.5% periodic acid solution for 10 min and rinsed with distilled water for 2-3 min. In a dark chamber, sections were treated with Schiff solution for 15-30 min. After rinsing with distilled water, sections were counterstained with hematoxylin .
Cell counting kit 8 (CCK8) assay
Cell viability was measured by conversion of Dojindo's highly water-soluble tetrazolium salt WST-8 to a yellow-colored watersoluble formazan (CCK8 assay). The amount of formazan dye generated by the activity of mitochondrial dehydrogenases in cells is directly proportional to the number of living cells. CCK8 is more sensitive than the 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide assay . SKOV3 cells were trypsinized and seeded at 5 × 103 cells/well in 96 well plates in 3D cultures. After 24 h, various concentrations of bevacizumab were added, followed by incubation for another 48 h. Then, 10 μL CCK8 (Sigma, USA) solution in PBS was added to each well. Plates were incubated for an additional 2 h. The optical density of each well was measured using a microculture plate reader at a 490 nm wavelength.
All results were evaluated using the SPSS 13.0 statistical software package. Data were analyzed using one-way ANOVA. Results were expressed as the mean ± standard deviation, and P < 0.05 was considered statistically significant.
Increased metastasis after short-term treatment with the angiogenesis Inhibitor bevacizumab
Hypoxia is implicated in the adaptive response
Anti-VEGF treatment also induces increased VM
In vitro experiment demonstrating the effect of bevacizumab on VM
Antiangiogenic therapy is one of the most significant advances in cancer treatment. Its clinical value has been investigated, but is still too limited. A number of recent clinical and preclinical observations have been reported. In a neoadjuvant phase II trial of advanced epithelial ovarian cancer patients treated with the combinational therapy of carboplatin/paclitaxel with the angiogenesis inhibitor sorafenib, Pölcher M et al. reported that progressive disease was diagnosed in two patients out of four, and surgical exploration showed an increased number of peritoneal tumor implants . Furthermore, after short-term treatment, varous forms of antiangiogenic therapy can lead to increased metastasis in mouse models of multiple tumor types [12, 13]. Thus, there is a strong need to improve treatment strategies and to better understand the mechanisms of failure that hinder targeted antiangiogenic therapies. Here, we address the effect of short-term bevacizumab treatment using ovarian cancer xenografts. The data show that short-term bevacizumab treatment induces a reduction in tumor growth and an increase in distant tumor metastasis as measured by bioluminescence. Importantly, similar results were obtained when nu/nu mice were treated with bevacizumab + cisplatin and cisplatin alone. It should be noted that in mouse models of ovarian cancer, antiangiogenic therapy can elicit an adaptive response involving increased dissemination and the emergence of distant metastasis.
To investigate this metastatic "conditioning" effect, a better understanding of the biological effects of anti-VEGF treatment is required. Antiangiogenic therapy inhibits the development of new blood vessels, i.e. angiogenesis, resulting in reduced perfusion and an increase in intratumoral hypoxia, which may indirectly affect the tumor cells by inducing a more invasive phenotype in response to hypoxia, leading to increased invasion and metastatic dissemination [14, 15]. HIF-1α is a main regulator of the transcriptional response of cancer cells to hypoxia. By analyzing HIF-1α expression using western blotting we showed that treatment with bevacizumab increases intratumoral hypoxia in metastasis models of ovarian cancer. While most tumors showed little or no expression of HIF-1α protein in groups without bevacizumab treatment, HIF-1α expression markedly increased both in bevacizumab and bevacizumab + cisplatin groups. In summary, short-term bevacizumab treatment results in increased of HIF-1α expression. Interestingly, HIF-1α regulates genes that are involved in angiogenesis, cell survival, invasion and metastasis . Therefore, downstream pathways of HIF-1α gene may contribute to metastatic phenotypes.
Current antiangiogenic strategies are mainly directed against tumor endothelial cells. However, tumours do not only rely on host blood vessels for nourishment, they can also form their own vasculature. The term "VM" has been used to describe the manner in which tumor cells mimic endothelial cells to form vasculogenic networks. VM has been described in ovarian cancer and some other highly aggressive tumors such as melanoma, prostatic carcinoma, breast cancer, soft tissue sarcomas and lung cancer [17–22]. The presence of VM correlates to an increased risk of metastasis and poor clinical outcome [23–26]. Several key molecules, including VE-cadherin, matrix metalloproteinases, laminin-5 γ2 chain and EphA2, have been implicated in VM. Moreover, the tumor microenvironment, including hypoxia, ischemia and acidosis, plays a major role in trans-endothelial differentiation of aggressive tumor cells [27–30]. In the hypoxic microenvironment, melanoma cells increase HIF-1α expression and induce the formation of VM channels to acquire an adequate blood supply . In 3D culture, bevacizumab treatment for up to 48 h did not affect SKOV3 cell viability and the ability to form VM. Moreover, our data showed more VM channels in short-term bevacizumab treatment groups than those in control groups. This feature suggests that VM channels, which cannot be inhibited by bevacizumab, may satisfy the vascular requirements of ovarian cancer growth, invasion and metastasis during hypoxia. Thus, the increased of VM formation as a result of bevacizumab-induced hypoxia may increase dissemination and the emergence of distant metastasis. These findings offer a possible explanation for why antiangiogenesis only shows transitory clinical benefits.
VEGF inhibition causes hypoxia, induces HIF-1α expression and the formation of VM, which may be associated with tumor invasion and metastasis. Antiangiogenesis inhibits endothelium-dependent vessels, and then causes hypoxia in tumors. To compensate for tumor hypoxia, VM may increase to maintain the tumor blood supply and provide a convenient route for tumor metastasis. Another question raised by our results is whether other mechanisms linked to the hypoxic response could contribute to the metastatic phenotype, such as angiogenesis, growth factor signaling and apoptosis. The relationship between antiangiogenic therapy and metastasis remains to be determined and is an important topic for future research. Further study may provide additional drug targets, resulting in adjuvant therapies that can enhance the clinical benefits of antiangiogenic treatment.
We thank Jing Zhou for technical assistance.
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