Primary tumorectomy promotes angiogenesis and pulmonary metastasis in osteosarcoma-bearing nude mice

6 – ORIGINAL ARTICLE

EXPERIMENTAL ONCOLOGY

Primary tumorectomy promotes angiogenesis and pulmonary metastasis in osteosarcoma-bearing nude mice¹

Zhi-Yuan Wang^I; Jiong Mei^II; You-Shui Gao^III; Ming Ni^IV; Bin Yao^v

^IDoctor degree, Department of Orthopedic Surgery, Tongji Hospital, Tongji University, Shanghai, China. Main author. Study design and manuscript preparation

^IIFull Professor, Department of Orthopedic Surgery, Tongji Hospital, Tongji University, Shanghai, China. Study design and manuscript preparation

^IIIDoctor degree, Department of Orthopedic Surgery, Shanghai Sixth People 's Hospital, Shanghai Jiao Tong University, Shanghai, China. Critical revision

^IVDoctor degree, Department of Orthopedic Surgery, Tongji Hospital, Tongji University, Shanghai, China. Technical procedures

^VDepartment of Orthopedic Surgery, Tongji Hospital, Tongji University, Shanghai, China. Statistical analysis

^{Correspondence}

ABSTRACT

PURPOSE: To investigate the effect of primary tumorectomy on angiogenesis and pulmonary metastasis in osteosarcoma-bearing nude mice.

METHODS: Osteosarcoma was introduced to nude mice via subcutaneous injection of MG-63 cells. One hundred and eighty osteosarcoma-bearing mice were used equally in 3 parallel experiments. The effect of tumorectomy (TR) on the expression of vascular endothelial growth factor (VEGF) and endostatin was investigated by ELISA. Meanwhile, the effect on angiogenesis was evaluated by Matrigel plug assay, and pulmonary metastasis assessed by calculating the metastatic foci. Sham-operation (SO) and untreated (UT) groups served as controls.

RESULTS: The VEGF (TR: 79.55 ± 7.82 pg/mL vs. SO: 110.01 ± 5.69 pg/mL, UT: 123.50 ± 10.41 pg/mL; p < 0.01) and endostatin (TR: 47.09 ± 6.22 ng/mL vs. SO: 117.64 ± 7.39 ng/mL, UT: 126.73 ± 6.55 ng/mL; p<0.01) were down-regulated significantly after tumorectomy, and angiogenesis was significantly promoted simultaneously. The incidence of pulmonary metastatic foci was 80.0% in the TR group, 40.0% in the SO group and 35.0% in the UT group.

CONCLUSION: Primary tumorectomy can down-regulate the expression of VEGF and endostatin and promote angiogenesis which leads to the acceleration of pulmonary metastasis. These findings imply that anti-angiogenic treatment can be considered after primary tumorectomy.

Key words: Osteosarcoma. Neplasm Metastasis. Vascular Endothelial Growth Factor A. Endostatins. Tumor Resistance. Mice.

Introduction

Osteosarcoma is a highly malignant tumor occurring frequently in children and young adults¹. Similar to other solid tumors, osteosarcoma often metastasizes to distant organs, especially the lung in early phase². Generally, the metastatic foci are always very small and may not cause symptoms, which makes the diagnosis difficult and leads to poor response to conventional treatments including surgical intervention and aggressive cytotoxic chemotherapy^3,4. Pulmonary metastasis is proved to be a major cause of death in patients suffering from osteosarcoma⁵. However, little is known about the exact mechanism underlying the spontaneous pulmonary metastasis of osteosarcoma. Several factors have been found to be associated with osteosarcoma metastasis in which concomitant tumor resistance (CTR) plays an important role^6-8. The CTR is a phenomenon in which a tumor-bearing host is resistant to the growth of secondary tumor implants and metastasis via the systemic angiogenic suppression. After primary tumorectomy, the angiogenesis and pulmonary metastasis might be accelerated^9,10.

A preliminary report has been published previously in which the relationship between tumorectomy and pulmonary metastasis was investigated¹¹. The present study aimed to investigate the effect of primary tumorectomy on angiogenesis and pulmonary metastasis in osteosarcoma-bearing nude mice and to explore the relationship among angiogenesis, pulmonary metastasis and primary tumorectomy. The probable mechanism and implication of CTR was also discussed on the basis of findings in the present study and previous studies.

Methods

This study was carried out in the Tongji University School of Medicine, Shanghai, China. The study was approved and in accordance with the Animal Welfare Regulations of TUMS. Nude mice (Balb/c, nu/nu) in the present study were purchased from the SLAC Laboratory Animal of Chinese Academy of Science (Shanghai, China). Mice were 5-week-old and had a body weight of 16~20g. They were housed in a specific pathogen-free environment at TUMS.

Cell culture

A human osteosarcoma cell line, MG-63 cells, was purchased from the American Typical Culture Collection (Manassas, VA) and maintained in RPMI-1640 (Gibco; Carlsbad, CA) containing 20% fetal bovine serum (FBS) at 37ºC in an environment with 5% CO₂. Cells were serially subcultured to 80% confluence, then digested and harvested for centrifugation at 1500 rpm for 5 min. The supernatant was removed, and the MG-63 cells were suspended in RPMI-1640 at a density of 1.0×10⁷ cells/mL. When cell viability was over 90%, 0.2 mL of cell suspension (2.0 × 10⁶ cells) was injected subcutaneously into the left forelimb of nude mice. Two weeks later, 180 cancer-bearing mice were randomly used in three parallel experiments (n=60 in each experiment) with three individual groups: tumorectomy (TR at left forelimb amputation) group, sham-operation (SO at right forelimb amputation) and untreated (UT) group.

Sampling and detection

On days 7, 14 and 21, five mice in each subgroup were anesthetized at each time point and blood (1.0 mL) was obtained. On day 21, five mice received left forelimb amputation in the TR group and right forelimb amputation in the SO group; and five mice were left untreated in the UT group. On day 28, five mice in five groups were anesthetized and 1.0 mL of blood was obtained. Plasma was prepared by centrifugation and allowed to keep at room temperature for 1h. Serum was educed overnight at 4ºC and centrifuged at 3000 rpm for 10 min. The supernatants were transferred and preserved. Enzyme-linked immunosorbent assay (ELISA) was employed to detect the content of VEGF and endostatin according to the manufacturer's instructions (VEGF kit: Invitrogen, Carlsbad, CA; endostatin kit: R&D, Minneapolis, MN).

On days 1, 7 and 14, 0.5 mL of Matrigel (BD; Bedford, MA) containing 200 ng of bFGF and 50 U of calparine was injected into subcutaneous tissue of five mice in each group. On day 21, five mice in each group were treated as above-mentioned. One week later, Matrigels were harvested and washed with normal saline thrice. Then, they were kept on dry ice for 12h and mixed with 0.5 mL of 0.01 g/L Triton-100 followed by incubation for l-2 h. The suspension was centrifuged at 1500 rpm for 10 min, and the supernatant was harvested. The sample (20 µL) was dissolved in 5 mL of Drabkin liquid (200 mg of K₃[Fe(CN)₆], 50 mg of KCN, 1 g of NaHCO₃ and 1000 mL of distilled water) followed by incubation for 40 min. The spectrophotometer was used to measure the absorbance (A) at 595 nm. The concentration of hemoglobin was calculated according to the following formula: Hb (g/L) = A × (64458/44000) × 251. The extent of angiogenesis was evaluated by the concentration of hemoglobin.

The osteosarcoma-bearing mice (n=20) in TR group received left forelimb amputation to remove the tumor completely, and mice in the SO and UT groups were treated as above-mentioned on day 14. Two weeks later, all mice were anesthetized and the lungs were removed. Mice with macroscopic pulmonary metastasis were recorded, and the incidence of metastasis was calculated individually. Then, pulmonary tissues were fixed in 10% formaldehyde and prepared for routine histological examination. Each experiment was performed in triplicate and found to be reproducible.

Statistical analysis

Statistical analysis was performed with SPSS 13.0 (Chicago, IL). Quantitative data were expressed as mean ± standard deviation (SD). One-way analysis of variance was employed to compare the means among groups. The least significant difference (LSD) was used to compare the means between two groups. A value of p<0.05 was considered statistically significant.

Results

After operation, the expression of endostatin and VEGF in the TR group decreased significantly when compared with the other two groups (VEGF: TR: 79.55 ± 7.82 pg/mL vs. SO: 110.01 ± 5.69 pg/mL, UT: 123.50 ± 10.41 pg/mL, p < 0.01; endostatin: 47.09 ± 6.22 ng/mL vs. 117.64 ± 7.39 ng/mL, 126.73 ± 6.55 ng/mL, p < 0.01) (Figures 1 and 2). There was no significant difference in the expression of VEGF and endostatin between SO group and UT group on days 7, 14, 21 and 28.

In the TR group, the content of hemoglobin in the Matrigel increased significantly as compared to the other two groups after surgery (TR: 38.25 ± 4.45 g/L vs. SO: 18.71 ± 1.33 g/L, UT: 17.90 ± 1.76 g/L; p < 0.01) (Figure 3). However, no significant difference in the hemoglobin content was found between SO group and UT group on days 7, 14, 21 and 28.

Additionally, in the TR group, 16 mice developed micrometastatic foci in the lung, which were found in only eight mice of SO group and seven mice of UT group. The incidence of pulmonary metastasis was 80.0%, 40.0% and 35.0% in the TR, SO and UT groups, respectively. Histologically, the severity of metastatic foci was higher in the TR group than in other two groups.

The endostatin level was relatively stable preoperatively and when the animals were treated non-operatively as well as by sham amputation. The level of endostatin in peripheral circulation was 117.64 ± 7.39 ng/mL and 126.73 ± 6.55 ng/mL in the SO group and UT group, respectively, after surgery. However, it significantly decreased to 47.09 ± 6.22 ng/mL after tumorectomy (p<0.01).

Hemoglobin was maintained at a stable level preoperatively and when the animals were treated non-operatively or by sham amputation. The level of hemoglobin in the Matrigel was 18.71 ± 1.33 g/L and 17.90 ± 1.76 g/L in the SO group and UT group, respectively, after surgery. However, it markedly increased to 38.25 ± 4.45 g/L after tumorectomy (p<0.01).

Discussion

Osteosarcoma is a highly malignant tumor that commonly affects children and young adults. Before wide application of neoadjuvant chemotherapy, approximately 80% of osteosarcoma patients develop systemic metastasis following surgical intervention. Even with multi-disciplinary treatment, more than half patients develop pulmonary metastasis, which has been a najor cause of death in patients with osteosarcoma⁶. Thus, it is imperative to develop measurements to diagnose and prevent pulmonary metastasis. Previous studies have showed that pulmonary metastasis of osteosarcoma is associated with the progression and termination of primary cancer. Kaya et al.¹² found that the removal of primary cancer could promote the progression of pulmonary metastasis of osteosarcoma. Such relationship between primary tumorectomy and metastasis has also been found in other solid tumors^13-17. Li et al.¹³ investigated the influence of tumorectomy on cancer growth in a cancer-bearing mouse model. They found that primary tumorectomy could accelerate the growth of pre-existing metastatic cancers which was probably related to multiple factors such as increases in angiogenesis and cancer cell proliferation and decrease in cancer cell apoptosis. Streck et al.¹⁴ compared the growth of metastatic liver cancer arising spontaneously from a subcutaneous cancer in mice, and results showed that the weight of metastatic liver cancer was significantly lower in mice without tumorectomy than in those undergoing primary tumorectomy. Compared with the rapid progression of micrometastatic cancer after primary tumorectomy, metastatic cancer always grow slowly provided that primary cancer is left intact. This distinct phenomenon that primary cancer is able to inhibit the growth of micrometastasis is known as CTR ⁹.

The exact mechanism of CTR is not well defined; however, there are several hypotheses to explain this unique phenomenon. Bashford et al.¹⁸ assumed that CTR was induced by immune reaction and called it "concomitant immunity". Several years later, investigators also identified this phenomenon in non-detectable immunogenicity or immunodeficient mice with cancer, and the term "concomitant immunity" was deserted^10,19. Prehn¹⁰ suggested that concomitant resistance could be reasonably explained by the competence of two co-existing cancers. Other hypotheses include nutrient deprivation and anti-mitogens secreted by primary cancers⁷. However, none of above-mentioned hypotheses can explain the molecular biology of concomitant resistance. Recently, some researchers propose that CTR is related to the angiogenic factors secreted by primary cancer^20,21. Scharovsky et al.¹⁵ found that CTR was associated with the ratio of angiogenic factors/anti-angiogenic factors. Kaya et al.¹² found the level of endostatin, an important antiangiogenic factor, decreased significantly after primary resection of osteosarcoma. In the present study, our results also revealed that the levels of VEGF and endostatin decreased dramatically after primary tumorectomy, which was coincident with previously reported.

VEGF and endostatin are both factors secreted by primary cancer and have different half-lives in the serum. The half-life of VEGF is relatively short, and the VEGF level decreases rapidly in the peripheral circulation. However, the half-life of endostatin is much longer and the endostatin can be maintained at a relatively stable level when the primary cancer is kept intact. As a result, a special antiangiogenic circumstance develops accordingly in the internal environment and micrometastasis is restricted from invading and growing. However, the levels of VEGF and endostatin decrease rapidly after primary tumorectomy, and thus the antiangiogenic environment disappears. The hypothesis is that the metastatic tumors may replace the primary tumor and exert antiangiogenetic effect. Undoubtedly, the efficacy could not help it to regain previous powerful steps and gradual pulmonary metastasis has been made on the agenda. Interestingly, Jia et al.²² found that the VEGF₁₆₅ was necessary for the metastatic potential of Fas^- osteosarcoma cells but unrelated to the metastasis of Fas⁺ cells. VEGF₁₆₅ expression decreased in LM7/siRNA₁₆₅ cells and increased in LM7/VEGF clones, while Fas was not correlated with these transfected clones. VEGF₁₆₅ is the strongest stimulator ofr angiogenesis, and the crosstalk of VEGF with other factors is required to be investigated further aiming to elucidate the molecular mechanism of spontaneous metastasis.

Based on our findings, we may speculate that it is necessary to consider additional antiangiogenic treatment after primary tumorectomy. The anti-angiogenic therapy represents a new approach to cure osteosarcoma and has several advantages as compared to traditional adjuvant chemotherapy. The anti-angiogenic therapy can inhibit the cancer growth through interrupting angiogenesis in cancers, and it is more selective and efficient than conventional chemotherapy. Meanwhile, the novel treatment may reduce the incidence of drug resistance because the target of angiogenic inhibitors is vascular endothelial cells which are genetically stable. It is supposed that favorable outcome might be achieved when anti-angiogenic treatment is applied in combination with neoadjuvant chemotherapy²³. Kaya et al.⁸ found that the angiogenic inhibitor (endostatin) could suppress the pulmonary metastasis of osteosarcoma after primary tumorectomy. The anti-angiogenic therapy has clinical significance in preventing pulmonary metastasis of osteosarcoma after primary tumorectomy ^24-26.

Received: October 15, 2012

Review: December 17, 2012

Accepted: January 18, 2013

Conflict of interest: none

Finance source: National Natural Science Foundation of China

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1

Research performed at Tongji University, School of Medicine, Shanghai, China.

Publication Dates

• Publication in this collection
  06 Mar 2013
• Date of issue
  Mar 2013

History

• Received
  15 Oct 2012
• Accepted
  18 Jan 2013
• Reviewed
  17 Dec 2012