In vitro modulation of MMP-2 and MMP-9 in adult human sarcoma cell lines by cytokines, inducers and inhibitors
- Authors:
- Published online on: September 30, 2013 https://doi.org/10.3892/ijo.2013.2113
- Pages: 1787-1798
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Copyright: © Roomi et al. This is an open access article distributed under the terms of Creative Commons Attribution License [CC BY_NC 3.0].
Abstract
Introduction
According to the American Cancer Society, ∼11,280 new soft tissue sarcomas would be diagnosed in 2012 (6,110 cases in males and 5,170 cases in females) and 3,900 Americans (2,050 males and 1,850 females) were expected to die of soft tissue sarcomas (1). Fibrosarcoma and liposarcoma are among the most common types of sarcoma in adults (1). Forty percent of primary bone cancers are chondrosarcomas, malignancies of cartilaginous origin, primarily affecting the cartilage cells of femur, arm, pelvis, knee and spine (2) and 4% of bone cancers are fibrosarcomas, aggressive and highly metastatic cancers of the connective tissue that primarily develops in metaphases of long tubular bones (2,3). Synovial sarcoma, accounting for <5–10% of all soft tissue sarcomas, develops in the synovial membrane of the joints, mainly in the lower limbs, but can also occur in the trunk and head/neck (4). Poor prognosis is attributed to both the aggressive metastatic spread characteristic of these cancers and the lack of efficacy in current treatment modalities to prevent or counteract tumor progression. The overall relative 5-year survival rate of people with soft tissue sarcomas is ∼50% according to statistics from the National Cancer Institute (1).
Numerous clinical and experimental studies have demonstrated that elevated levels of MMPs are associated with tumor growth, cancer progression, metastasis and shortened survival in patients (4,5). Among various MMP types, MMP-2 and MMP-9 play pivotal roles in tumor cell invasion and metastasis by degradation of type IV collagen, a major component of the ECM (6–8). MMP-2 (72 kDa) and MMP-9 (92 kDa) are secreted in their latent zymogenic form and cleaved by other MMPs or proteases to yield the activated forms of 68, 58 and 54 kDa for MMP-2 and 94 kDa for MMP-9.
MMP activity is regulated by and dependent upon environmental influences from surrounding stroma cells, ECM proteins, systemic hormones and other factors (6,9,10). A variety of cytokines and growth factors, such as transforming growth factor (TGF-β), hepatocyte growth factor (HGF), epidermal growth factor (EGF) and tumor necrosis factor (TNF-α) also control MMP activity (11,12). One of the most potent inducers of cancer cell proliferation is the chemical agent phorbol 12-myristate 13-aceteate (PMA). In addition, activity of MMPs is regulated at multiple levels, including transcription, modulation of messenger RNA half-life (translation), secretion, localization, activation and inhibition (13). There is little information available on the effects of various biological and chemical inducers and inhibitors in sarcomas. Among the few studies available, Rutkowski et al (14) investigated the correlations between serum levels of selected pro-inflammatory, hematopoietic and angiogenic cytokines and soluble cytokine receptors with the clinicopathological features and prognosis in soft tissue sarcoma patients. They found significant correlations of serum cytokine levels with tumor size and grade suggesting cytokines may be directly or indirectly involved in the progression of soft tissue sarcomas.
In this study, we investigated the effects of selected cytokines, inducers and inhibitors affecting cancer cell metabolism on the regulation of MMP-2 and MMP-9 activities in chondrosarcoma, fibrosarcoma, liposarcoma and synovial sarcoma cell lines.
Materials and methods
Materials
Human adult sarcoma cell lines chondrosarcoma (SW-1353), fibrosarcoma (HT-1080), liposarcoma (SW-872) and synovial sarcoma (SW-982) along with their culture media were obtained from ATCC. Antibiotics, penicillin and fetal bovine serum (FBS), were obtained from Gibco (BRL, Long Island, NY, USA). Twenty-four well tissue culture plates were obtained from Costar (Cambridge, MA, USA). Gelatinase zymography was performed in 10% Novex pre-cast SDS polyacrylamide gel (Invitrogen Inc.) with 0.1% gelatin in non-reducing conditions. Interleukin 1β (IL-1β), tumor necrosis factor-α (TNF-α), PMA, lipopolysaccharide (LPS), doxycycline, epigallocatechin gallate (EGCG), cyclohexamide, actinomycin-D, retinoic acid and dexamethasone, were purchased from Sigma (St. Louis, MO, USA). The nutrient mixture (NM), prepared by VitaTech (Hayward, CA, USA) was composed of the following ingredients in the relative amounts indicated: Vitamin C (as ascorbic acid and as Mg, Ca and palmitate ascorbate) 700 mg; L-lysine 1000 mg; L-proline 750 mg; L-arginine 500 mg; N-acetyl cysteine 200 mg; standardized green tea extract (80% polyphenol) 1000 mg; selenium 30 µg; copper 2 mg; manganese 1 mg. All other reagents used were of high quality and were obtained from Sigma, unless otherwise indicated.
Cell cultures
The sarcoma cell lines were grown in their respective media: fibrosarcoma in MEM, chondrosarcoma in DEM, liposarcoma in MEM and synovial sarcoma in DME, supplemented with 10% FBS, penicillin (100 U/ml) and streptomycin (100 µg/ml) in 24-well tissue culture plates. The cells were plated at a density of 1x105 cells/ml and grown to confluency in a humidified atmosphere at 5% CO2 at 37°C. Serum-supplemented media were removed and the cell monolayer was washed once with PBS and with the recommended serum-free media. The cells were then incubated in 0.5 ml of serum-free medium with various cytokines, mitogens, inducers and inhibitors in triplicates, as indicated: PMA (10, 25, 50, 100 ng/ml); TNF-α (0.1, 1, 10, 25 ng/ml); IL-1β (0.1, 1, 10, 25 ng/ml); LPS (10, 25, 50, 100 µg/ml); EGCG (10, 25, 50, 100 µM) without and with PMA 100 ng/ml; doxycycline (10, 25, 50, 100 µM) without and with PMA 100 ng/ml; NM (10, 50, 100, 500, 1000 µg/ml) with PMA 100 ng/ml, TNF-α 10 ng/ml, or IL-1β 10 ng/ml; retinoic acid (50 µM); dexamethasone (50 µM); actinomycin-D (2 and 4 µg/ml); and cyclohexamide (2 and 4 µg/ml). The plates were then returned to the incubator. The conditioned medium from each treatment was collected separately, pooled and centrifuged at 4°C for 10 min at 3000 rpm to remove cells and cell debris. The clear supernatant was collected and used for gelatinase zymography, as described below.
Gelatinase zymography
Gelatinase zymography was utilized because of its high sensitivity to gelatinolytic enzymatic activity and ability to detect both pro and active forms of MMP-2 and MMP-9. Upon renaturation of the enzyme, the gelatinases digest the gelatin in the gel and reveal clear bands against an intensely stained background. Gelatinase zymography was performed in 10% Novex pre-cast SDS polyacrylamide gel in the presence of 0.1% gelatin under non-reducing conditions. Culture media (20 µl) were mixed with sample buffer and loaded for SDS-PAGE with tris glycine SDS buffer, as suggested by the manufacturer (Novex). Samples were not boiled before electrophoresis. Following electrophoresis the gels were washed twice in 2.5% Triton X-100 for 30 min at room temperature to remove SDS. The gels were then incubated at 37°C overnight in substrate buffer containing 50 mM Tris-HCl and 10 mM CaCl2 at pH 8.0 and stained with 0.5% Coomassie Blue R250 in 50% methanol and 10% glacial acetic acid for 30 min and destained.
Protein standards were run concurrently and approximate molecular weights were determined by plotting the relative mobilities of known proteins. Gelatinase zymograms were scanned using CanoScan 9950F Canon scanner at 300 dpi. The intensity of the bands was evaluated using the pixel-based densitometer program Un-Scan-It, version 5.1, 32-bit, by Silk Scientific Corp. (Orem, UT, USA), at a resolution of 1 Scanner Unit (1/100 of an inch for an image that was scanned at 100 dpi).
Results
Inducers and cytokines
Table I shows the quantitative densitometry results from the effects of PMA, TNF-α, IL-1β and LPS on MMP-2 and MMP-9 expression in chondrosarcoma, fibrosarcoma, liposarcoma and synovial sarcoma cell lines
Effect of PMA, TNF-α, IL-1β and LPS on MMP-2 and MMP-9 expression in chondrosarcoma SW-1353 cell line
On gelatinase zymography, SW-1353 cells demonstrated strong expression of MMP-2 and slight expression of MMP-9. PMA treatment had no significant effect on expression of MMP-2 but stimulated MMP-9 expression in a dose-dependent manner (linear trend R2=0.9673), as shown in Fig. 1. TNF-α had a stimulatory effect on MMP-9 (linear trend R2=0.5135) and insignificant effect on MMP-2. IL-1β stimulated MMP-9 and MMP-2. LPS showed slight stimulation of MMP-2 but no significant effect on MMP-9.
Effect of PMA, TNF-α, IL-1β and LPS on MMP-2 and MMP-9 expression in fibrosarcoma HT-1080 cell line
On gelatinase zymography, HT-1080 cells demonstrated strong expression of MMP-2 inactive and faint MMP-2 active, both greater than MMP-9. PMA treatment strongly stimulated MMP-9 expression in a dose-dependent manner (linear trend R2=0.7952) and slightly enhanced MMP-2 active and inhibited MMP-2 inactive, as shown in Fig. 2. TNF-α had a strong stimulatory dose-dependent effect on MMP-9 and a slight enhancement of MMP-2. IL-1β slightly stimulated MMP-9 and had no discernible effect on MMP-2. LPS showed slight stimulation of MMP-2 but no significant effect on MMP-9.
Effect of PMA, TNF-α, IL-1β and LPS on MMP-2 and MMP-9 expression in liposarcoma SW-872 cell line
On gelatinase zymography, SW-872 cells demonstrated MMP-2 and MMP-9 expression. PMA treatment strongly stimulated MMP-9 expression in a dose-dependent manner (linear trend R2=0.617) but had no significant effect on MMP-2, as shown in Fig. 3. TNF-α had a strong stimulatory dose-dependent effect on MMP-9 (linear trend R2=0.6358) and a slight reduction in MMP-2. IL-1β slightly stimulated MMP-9 expression at 1 and 10 ng/ml, then inhibited it at 25 ng/ml and inhibited MMP-2 in dose-dependent manner (linear trend R2=0.865). LPS showed slight dose-dependent inhibition in MMP-2, except at 50 ng/ml, but no significant effect on MMP-9.
Effect of PMA, TNF-α, IL-1β and LPS on MMP-2 and MMP-9 expression in synovial sarcoma SW-982 cell line
On gelatinase zymography, SW-982 cells demonstrated moderate MMP-2 and no MMP-9 expression. PMA treatment strongly stimulated MMP-9 expression in a dose-dependent manner (linear trend R2=0.672) and slightly inhibited MMP-2 expression (linear trend R2=0.797), as shown in Fig. 4. TNF-α had a moderate inhibitory dose-dependent effect on MMP-2 (linear trend R2=0.425) and a slight stimulatory effect on MMP-9 at the highest dose tested, 10 ng/ml (linear trend R2=0.425). IL-1β had no significant effect on MMP-2 or MMP-9 expression. The effects of LPS were not determined.
Chemical inhibitors
Table II shows the quantitative densitometry results from the effects of chemical inhibitors doxycycline, dexamethasone, actinomycin-D and cyclohex-amide on MMP-2 and MMP-9 expression in chondrosarcoma, fibrosarcoma, liposarcoma and synovial sarcoma cell lines
Effect of chemical inhibitors: doxycycline, dexamethasone, actinomycin-D and cyclohexamide on MMP-2 and MMP-9 expression in chondrosarcoma SW-1353 cell line
On gelatinase zymography, SW-1353 cells demonstrated strong expression of MMP-2 and slight expression of MMP-9, with enhanced MMP-9 expression with PMA (100 ng/ml) treatment. Doxycycline with and without PMA (100 ng/ml) treatment showed dose-dependent inhibition of MMP-2 and MMP-9 (linear trends R2=0.894 and 0.910, respectively). MMP-2 was inhibited by 99% and MMP-9 by 96% at 100 µM doxycycline compared to control; PMA-treated SW-1353 showed dose-dependent inhibition of MMP-9 (R2=0.785) with doxycycline treatment compared to control and no significant change in MMP-2. Actinomycin-D showed dose-dependent inhibition of both MMP-2 and -9 (linear trends R2=0.804 and 0.785, respectively). Cyclohexamide showed dose-dependent inhibition of both MMP-2 and -9 (linear trends R2=0.768 and 0.750, respectively). Dexamethasone 50 µM demonstrated no effect on MMP-2 but inhibition of MMP-9.
Effect of chemical inhibitors: doxycycline, dexamethasone, actinomycin-D and cyclohexamide on MMP-2 and MMP-9 expression in fibrosarcoma HT-1080 cell line
On gelatinase zymography, normal HT-1080 cells demonstrated strong expression of MMP-2 with PMA-induced expression of MMP-9. Doxycycline treatment of HT-1080 cells showed dose-dependent inhibition of MMP-2 and MMP-9 (linear trends R2=0.780 and 0.798, respectively). PMA-treated HT-1080 showed dose-dependent inhibition of MMP-9 (R2=0.543) with doxycycline treatment compared to control and no significant change in MMP-2. Actinomycin-D showed dose-dependent inhibition of MMP-2 (linear trend R2=0.978). Dexamethasone 50 µM demonstrated no effect on MMP-9 but inhibited MMP-2 by 38%. The effect of cyclohexamide was not determined.
Effect of chemical inhibitors: doxycycline, dexamethasone, actinomycin-D and cyclohexamide on MMP-2 and MMP-9 expression in liposarcoma SW-872 cell line
On gelatinase zymography, normal SW-872 cells demonstrated MMP-2 and MMP-9 expression. Doxycycline treatment of SW-872 cells showed enhanced secretion of MMP-9 at 10 and 25 µM and inhibition of MMP-9 at 50 and 100 µM. MMP-2 expression was not appreciably affected at lower concentrations of doxycycline, but was significantly inhibited at 50 and 100 µM (linear trend R2=0.739). PMA-treated SW-872 cells showed dose-dependent inhibition of MMP-9 (R2=0.922) with doxycycline treatment compared to control and no significant change in MMP-2. Dexamethasone 50 µM inhibited SW-873 secretion of MMP-2 by 84% and MMP-9 by 99%. The effects of cyclohexamide and actinomycin-D were not determined.
Effect of chemical inhibitors doxycycline, dexamethasone, actinomycin-D and cyclohexamide on MMP-2 and MMP-9 expression in synovial sarcoma SW-982 cell line
On gelatinase zymography, normal SW-982 cells demonstrated strong expression of MMP-2 and undetectable level of MMP-9. The effects of doxycycline, actinomycin-D, dexamethasone, cyclohexamide and retinoic acid on SW-982 cell expression of MMP-2 and -9 were not determined.
Natural inhibitors
Table III shows the quantitative densitometry results from the effects of natural inhibitors EGCG, the NM and retinoic acid on MMP-2 and MMP-9 expression in chondrosarcoma, fibrosarcoma, liposarcoma and synovial sarcoma cell lines.
Effect of EGCG, nutrient mixture and retinoic acid on MMP-2 and MMP-9 expression in chondrosarcoma SW-1353 cell line treated with inducers
On gelatinase zymography, SW-1353 cells demonstrated strong expression of MMP-2 and slight expression of MMP-9. EGCG inhibited MMP-9 and MMP-2 in a dose-dependent manner, with total inhibition of MMP-2 and 95% inhibition of MMP-9 at 100 µM (linear trends R2=0.809 and 0.933, respectively). NM inhibited MMP secretion in a dose-dependent manner with virtual total inhibition of MMP-9 at 500 µg/ml (linear trend R2=0.713) and MMP-2 at 1000 µg/ml (linear trend R2=0.860). PMA (100 ng/ml) treatment profoundly enhanced MMP-9 expression. EGCG inhibited MMP-9 and MMP-2 in a dose-dependent manner, with total inhibition of MMP-9 and 96% inhibition of MMP-2 at 100 µM (linear trends R2=0.892 and 0.336, respectively), as shown in Fig. 5. NM demonstrated dose-dependent inhibition of MMP-2 and MMP-9 expression levels of PMA-treated SW-1353 total block of MMP-2 and virtually total inhibition of MMP-9 secretion at 1000 µg/ml (linear trends R2=0.831 and 0.833, respectively), as shown in Fig. 6. SW-1353 cells treated with TNF-α (10 ng/ml) showed strong expression levels of MMP-9 and MMP-2. TNF-α-treated cells showed slight stimulation of MMP-2 and -9 at low concentrations of NM and strong inhibition at concentrations of NM 100 µg/ml and higher, with linear trends R2=0.796 and 0.641, respectively, as shown in Fig. 7. SW-1353 cells treated with IL-1β (10 ng/ml) showed strong expression of MMP-9 and slight expression of MMP-2. NM treatment of IL-1 β -treated cells showed enhanced expression of both MMPs at low concentrations of NM and strong inhibition of both MMP-2 and MMP-9 at concentrations of NM 100 µg/ml and higher, as shown in Fig. 8. Retinoic acid showed strong inhibition of MMP-2 and MMP-9 at the dose tested (50 µM).
Effect of EGCG, the nutrient mixture and retinoic acid on MMP-2 and MMP-9 expression in fibrosarcoma HT-1080 cell line treated with inducers
On gelatinase zymography, normal HT-1080 cells demonstrated strong expression of MMP-2 with PMA-induced expression of MMP-9. EGCG inhibited MMP-2 in a dose-dependent manner, with linear trend R2=0.720; PMA-treated HT-1080 cells showed MMP-2 and induced MMP-9 expression, which were inhibited in a dose-dependent manner, with linear trends R2=0.452 and 0.475, respectively, as shown in Fig. 9. NM inhibited secretion of MMP-2 and MMP-9 by uninduced HT-1080 cells in a dose-dependent manner, with linear trends R2=0.510 and 0.546, respectively. NM showed dose-dependent inhibition of MMP-2 and -9 expression in PMA-treated cells with linear trends R2=0.866 and 0.678, respectively, as shown in Fig. 10. HT-1080 cells treated with TNF-α (10 ng/ml) showed strong expression levels of MMP-9 and MMP-2. TNF-α-treated cells showed slight stimulation of MMP-2 and -9 at low concentrations of NM and strong inhibition at concentrations of NM 100 µg/ml and higher, with linear trends R2=0.880 and 0.855, respectively, as shown in Fig. 11. HT-1080 cells treated with IL-1β (10 ng/ml) showed a strong expression of MMP-9 greater than MMP-2. NM treatment of IL-1β-treated cells showed dose-dependent inhibition of both MMP-2 and MMP-9, with linear trends R2=0.934 and 0.861, respectively, as shown in Fig. 12. The effect of retinoic acid was not determined.
Effect of EGCG, the nutrient mixture and retinoic acid on MMP-2 and MMP-9 expression in liposarcoma SW-872 cell line treated with inducers
On gelatinase zymography, SW-872 cells demonstrated MMP-2 and strongly stimulated MMP-9 with PMA (100 ng/ml) treatment. EGCG inhibited both MMP-2 and -9 in a dose-dependent manner, with linear trends R2=0.914 and 0.787, respectively; PMA (100 ng/ml)-treated SW-872 cells showed MMP-2 and strongly enhanced MMP-9 expression, which were inhibited by EGCG in a dose-dependent manner, with linear trends R2=0.560 and 0.782, respectively, as shown in Fig. 13. NM treatment of SW-872 cells treated with PMA showed dose-dependent inhibition of MMP-2 and MMP-9, with linear trends R2=0.820 and 0.898, respectively, as shown in Fig. 14. The effects of retinoic acid were not determined.
Effect of natural inhibitors: EGCG, the nutrient mixture and retinoic acid on MMP-2 and MMP-9 expression in synovial sarcoma SW-892 cell line treated with inducers
On gelatinase zymography, SW-892 cells showed strong MMP-2 expression and induction of MMP-9 with PMA (100 ng/ml) treatment. EGCG inhibited MMP-2 in a dose-dependent manner, with linear trend R2=0.878; PMA (100 ng/ml)-treated SW-982 cells showed MMP-2 and induced MMP-9 expression, which were inhibited by EGCG in a dose-dependent manner, with linear trends R2=0.881 and 0.459, respectively, as shown in Fig. 15. SW-982 cells treated with PMA showed dose-dependent inhibition of MMP-2 and MMP-9 expression with NM treatment, with linear trends, R2=0.855 and 0.694, respectively, as shown in Fig. 16. Effects of retinoic acid were not determined.
Discussion
Experimental and clinical studies have shown a correlation between increased MMPs and tumor progression and metastasis (6,7). Thus, knowledge of MMP regulation is of importance for developing therapeutic strategies. MMP expression is regulated at both pre- and post-transcriptional levels. Extracellular factors, including cytokines, growth factors and inducers and inhibitors, have been implicated in the regulation of MMP expression in different types of tumor cells (15,16). Though few cytokine and growth factor studies have been conducted on sarcomas, some research has documented elevated serum levels of VEGF, IL-2 and bFGF in sera of patients with soft tissue sarcomas (17,18); VEGF serum levels correlated significantly with tumor size and histological grade (17). Serum cytokine levels significantly correlated with tumor size and grade suggesting involvement of cytokines in the progression of soft tissue sarcomas (14). Rutkowski et al found elevated cytokines and soluble cytokine receptors involved in bone destruction and bone formation in 46% of adult bone sarcoma patients, suggesting they have an essential role in the progression of malignant bone tumors (19).
In this study, we compared MMP secretion patterns by cytokines, PMA and LPS in four adult sarcoma cell lines that express MMP-2 and MMP-9 to different extents. In addition, we investigated the effect of inhibitors doxycycline and EGCG and others, such as dexamethasone, retinoic acid and agents that affect transcription and translation levels, such as actinomycin-D and cyclohexamide. Furthermore, we tested a nutrition mixture that had inhibitory effects on MMP-2 and MMP-9 expression. We found that fibrosarcoma HT-1080, chondrosarcoma SW-1353, liposarcoma SW-872 and synovial sarcoma SW-982 normally expressed both MMP-2 and MMP-9. Treatment of all these cell lines with PMA strongly upregulated expression of MMP-9 in a dose-dependent manner. However, the effect on MMP-2 was variable; PMA-treated fibrosarcoma and chondrosarcoma cells showed slightly stimulated MMP-2 expression, while PMA showed no effect on liposarcoma expression of MMP-2 and inhibition of MMP-2 was seen in PMA treatment of synovial sarcoma. TNF-α had an inhibitory effect at 0.1-10 ng/ml and a stimulatory effect at 25 ng/ml on MMP-9 and an inhibitory effect at 0.1 ng/ml and stimulatory effect at 10–25 ng/ml on MMP-2 in chondrosarcoma SW1353 cells. In fibrosarcoma cells TNF-α strongly stimulated MMP-9 and slightly stimulated MMP-2. In liposarcoma cells, TNF-α strongly stimulated MMP-9 and showed slight up and down activity on MMP-2. Synovial sarcoma showed inhibition of MMP-2 with TNF-α and slight stimulation of MMP-9 at 10 ng/ml. IL-1β stimulated MMP-9 and MMP-2 in chondrosarcoma cells, enhanced levels of both MMPs at 1 ng/ml but decreased levels at 25 ng/ml in fibrosarcoma, inhibited MMP-2 and enhanced MMP-9 at 1 and 10 ng/ml and downregulated at 25 ng/ml in liposarcoma cells. LPS showed slight stimulation of MMP-2 in chondrosarcoma and fibrosarcoma and slight inhibition of MMP-2 in lipo sarcoma, but no significant effect on MMP-9 in these cell lines.
Doxycycline and EGCG inhibited MMP-2 and MMP-9 expression in a dose-dependent fashion in all cell lines tested. Sensitivity to doxycycline was nearly equivalent in MMP-2 expression, but fibrosarcoma expression of MMP-9 was significantly more sensitive to doxycycline than were the other cell lines. MMP-2 expression was downregulated by 99% by doxycycline 100 µM in chondrosarcoma by 100% in fibrosarcoma and by 99% in liposarcoma. MMP-9 expression was downregulated by doxycycline 100 µM in chondrosarcoma and liposarcoma by 96 and 86%, respectively, while fibrosarcoma MMP-9 expression was completely blocked at 25 µM. Sensitivity of cell lines to EGCG varied in MMP-2 expression, with total block at 25 µM in synovial sarcoma, 50 µM in fibrosarcoma and liposarcoma and 96% block in chondrosarcoma at 100 µM. PMA-induced MMP-9 expression was blocked by EGCG at 25 µM in synovial sarcoma and 100 µM in fibrosarcoma and virtually blocked at 100 µM in chondrosarcoma and liposarcoma. Actinomycin-D, cyclohexamide, retinoic acid and dexamethasone inhibited MMP-2 and -9 in chondrosarcoma and fibrosarcoma cells.
The nutrition mixture inhibited MMP-2 and MMP-9 expression in a dose-dependent fashion in all PMA-treated cell lines. Synovial sarcoma was most sensitive to NM with block of MMP-2 at 500 µg/ml and MMP-9 at 100 µg/ml. Liposarcoma showed block of MMP-2 at 500 µg/ml and MMP-9 at 1000 µg/ml, while fibrosarcoma and chondrosarcoma showed block of MMP-2 at 1000 µg/ml and virtual block of MMP-9 at 1000 µg/ml. MMP-2 and-9 expression of chondrosarcoma and fibrosarcoma cells treated with TNF-α 10 ng/ml were downregulated by NM treatment in a dose-dependent manner with MMP-2 block at 1000 µg/ml NM and MMP-9 total block at 500 µg/ml NM in fibrosarcoma and 99% block at 1000 µg/ml in chondrosarcoma. MMP-2 and-9 expression of chondrosarcoma and fibrosarcoma cells treated with IL-1β 10 ng/ml were downregulated by NM treatment in a dose-dependent manner with MMP-2 block at 1000 µg/ml NM and MMP-9 total block at 100 µg/ml NM in fibrosarcoma and at 1000 µg/ml in chondrosarcoma.
The nutrition mixture studied, which contains lysine, proline, ascorbic acid and green tea extract among other micro-nutrients, has been shown to have anti-tumor and anti-invasive potential in vivo and in vitro (20). Of interest, a previous study demonstrated significant correlation between NM inhibition of Matrigel invasion and NM modulation of the MMP-2 and -9 activities of the sarcoma cell lines studied (21). Significant negative correlations were found between NM modulation of Matrigel invasion inhibition and MMP-2 secretion with fibrosarcoma HT-1080 (r= −0.911), chondrosarcoma SW-1353 (r= −0.942), liposarcoma SW-872 (r= −0.957) and synovial sarcoma SW-982 (r= −0.878). Previous in vivo studies of the dietary effects of NM 0.5% on xenograft tumor growth of fibrosarcoma and synovial sarcoma cells in nude mice support these results in that they demonstrated significant inhibition of xenograft tumor growth: 59%, p=0.0005 in fibrosarcoma HT-1080 xenografts (22) and 44%, p=0.01 in synovial sarcoma Hs 701.T xenografts (23).
NM was designed by focusing on physiological targets in cancer progression and metastasis as documented in clinical and experimental studies. The nutrient mixture was formulated by selecting nutrients that act on critical physiological targets in cancer progression and metastasis, as documented in both clinical and experimental studies. Combining these micro-nutrients expands metabolic targets, maximizing biological impact with lower doses of components. A previous study of the comparative effects of NM, green tea extract and EGCG on inhibition of MMP-2 and MMP-9 secretion of different cancer cell lines with varying MMP secretion patterns, revealed the superior potency of NM over GTE and EGCG at equivalent doses (24). These results can be understood from the more comprehensive treatment offered by the combination of nutrients in NM over individual components of NM since MMP-2 and MMP-9 are mediated by differential pathways.
Optimal ECM structure depends upon adequate supplies of ascorbic acid and the amino acids lysine and proline to ensure proper synthesis and hydroxylation of collagen fibers. In addition, lysine contributes to ECM stability as a natural inhibitor of plasmin-induced proteolysis (25,26). Manganese and copper are also essential for collagen formation. There is considerable documentation of the potency of green tea extract in modulating cancer cell growth, metastasis, angiogenesis and other aspects of cancer progression (27–31). N-acetyl cysteine and selenium have demonstrated inhibition of tumor cell MMP-9 and invasive activities, as well as migration of endothelial cells through ECM (32–34). Ascorbic acid demonstrates cytotoxic and antimetastatic actions on malignant cell lines (35–39) and cancer patients have been found to have low levels of ascorbic acid (40,41). Low levels of arginine, a precursor of nitric oxide (NO), can limit the production of NO, which has been shown to predominantly act as an inducer of apoptosis (42).
In conclusion, our results show that cytokines and inhibitors regulate MMP-2 and MMP-9 expression in adult sarcoma cell lines, suggesting the clinical value of targeting these proteases for management of sarcomas and their pathogenesis.
Acknowledgements
This study was funded by Dr. Rath Health Foundation (Santa Clara, CA), a non-profit organization.
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