Background
Chondrosarcoma is the second most common malignancy of bone and it has a poor response to chemotherapy or radiation treatment currently-used, making the management of chondrosarcomas a complicated challenge [
1]. Clinically, surgical resection remains the primary mode of therapy for chondrosarcoma. In the absence of an effective adjuvant therapy, this mesenchymal malignancy has a poor prognosis and therefore, it is important to explore novel and adequate remedies [
2]. Since chondrosarcoma is a type of highly malignant tumor with a potent capacity to invade locally and metastasize distantly [
2], an approach that decreases its ability to invade and metastasize may facilitate the development of effective adjuvant therapy.
Cyclooxygenases (COXs) are the rate-limiting enzymes that catalyze the conversion of arachidonic acid to prostaglandins (PGs). Two COX isoforms with distinct tissue distributions and physiological functions have been identified [
3]. COX-1 is constitutively expressed in many tissues and plays important roles in the control of homeostasis [
4]. Conversely, COX-2 is an inducible enzyme and is activated by extracellular stimuli such as growth factors and pro-inflammatory cytokines [
5]. Recent investigations indicated that over-expression of COX-2 is frequently found in many types of cancer, including colon, lung, breast, pancreas, head and neck cancers [
6‐
9], and is usually associated with poor prognosis and short survival. Identification of four subtypes of the PGE receptor (EP1-EP4) has made it possible to analyze their effects on human cancer cells [
10,
11]. Studies have shown that EP1 is coupled to Ca
2+ mobilization; EP2 and EP4 activate adenylate cyclase, whereas EP3 inhibits adenylate cyclase [
12‐
14]. Furthermore, these studies indicated that cancer cells express multiple subtypes of the PGE receptor and that each subtype might be linked to different actions of PGE
2.
Tumor invasion and metastasis are the critical steps in determining the aggressive phenotype of human cancers. Mortality in cancer patients principally results from metastatic spread of cancer cells to distant organs [
15]. Integrins are a family of transmembrane adhesion receptors comprising 19α and 8β subunits that interact noncovalently to form up to 24 different heterodimeric receptors [
16]. The combination of different integrin subunits on the cell surface allows cells to recognize and respond to a variety of different extracellular matrix proteins including fibronectin, laminin, collagen and vitronectin [
16]. Activation and elevated expression of integrin-coupled signaling effectors have been implicated in the induction of a wide variety of human cancers, including those of the breast, colon, prostate, and ovaries [
17‐
19]. In addition, integrin has also been implicated in metastasis of lung, breast, bladder and colon cancers [
20‐
22].
The contribution of COX-2 to tumorigenesis has been intensively studied. Previous studies have shown that COX-2 modulates cell migration and invasion in several types of cancer cells [
23,
24]. Interaction of COX-2 with its specific EP receptors on the surface of cancer cells has been reported to induce cancer invasion [
25]. However, the effect of COX-2 and EP receptors on migration activity in human chondrosarcoma cells is mostly unknown. Here we found the mRNA expressions of COX-2 and EP1 receptor in chondrosarcoma patients and chondrosarcoma cell lines were significantly higher than in normal cartilage. COX-2 and PGE
2 also increased the migration and α2β1 integrin up-regulation of human chondrosarcoma cells. In addition, EP1 receptor, phospholipase Cβ3 (PLCβ3), protein kinase Cα (PKCα), c-Src and NF-κB signaling pathways were involved.
Discussion
The elucidation of the molecular biology of cancer cells in recent years has identified various molecular pathways that are altered in different cancers. This information is currently being exploited to develop potential therapeutic targets. To achieve metastasis, cancer cells must evade or co-opt multiple rules and barriers. Several discrete steps are discernible in the biological cascade of metastasis: loss of cellular adhesion, increased motility and invasiveness, entry and survival in circulation, exit into new tissue, and eventual colonization of a distant site [
30]. The mechanism of metastasis is a complicated and multistage process. Here, we provide evidence that α2β1 integrin acts as a crucial transducer of cell signaling, regulating cell migration and COX-2 act as a critical mediator of the metastatic activity of cancer cells in the tumor microenvironment. In addition, α2β1 integrin mAb, U73122, GF109203X, PP2, PDTC, TPCK, PLC siRNA, PKC mutant, c-Src mutant, IKKα mutant and IKKβ mutant reduced PGE
2-mediated cell migration in SW1353 cells (Additional file
1 - Figure S1). Furthermore, U73122, GF109203X, PP2, PDTC and TPCK also abolished PGE
2-increased α2β1 integrin expression in SW1353 cells (Additional file
2 - Figure S2). Therefore, the same signaling pathways are involved in all chondrosarcoma cells. Moreover, α2β1 integrin mAb, U73122, GF109203X, PP2, PDTC, TPCK and EP1 siRNA reduced PGE
2-mediated cell invasion in JJ012 cells [Transwell filters were precoated with Matrigel basement membrane matrix (BD Biosciences, Bedford, MA)] (Additional file
3 - Figure S3). Therefore, the same signaling pathways are involved in PGE
2-mediated cell invasion in human chondrosarcoma cells.
COX-2 is a pleiotropic enzyme that mediates many physiological functions such as inhibition of cell apoptosis, augmentation of angiogenesis, as well as increased cell motility. These COX-2-mediated functions are mediated in part by various genes such as B-cell lymphoma-2 [
31], myeloid cell leukemia-1, VEGF-A [
32] and metalloproteinases [
33]. However, the effect of COX-2 on migration activity in human chondrosarcoma cells is mostly unknown. Using qPCR analysis, we found that the expression of mRNA levels of COX-2 in human chondrosarcoma tissues and chondrosarcoma cell lines were significantly higher than those in normal cartilage. In this study, we used osteoarthritic cartilage to referee normal cartilage. However, cartilage from osteoarthritic patients may up-regulation COX-2 compared with normal cartilage. Therefore, the expression of COX-2 between normal cartilage, osteoarthritic cartilage and chondrosarcoma needs further examination. On the other hand, most of patient samples were isolated from low grade chondrosarcoma patients. Notably, grade 1 chondrosarcomas are not considered clinically overtly malignant or even locally aggressive lesion. Therefore, it might be possible that increased COX-2 expression was a result of inflammation for metaplasia. The expression of COX-2 in high grade chondrosarcomas are needed further examination. Moreover, primary chondrosarcoma cells and SW1353 or JJ012 cell lines were more migratory than normal chondrocyte. Our data provided the evidence that the expression of COX-2 is associated with a metastatic phenotype of chondrosarcoma cells. COX-2 exert it effects through interaction with specific EP1-4 receptors [
10‐
14]. However, the expression of EP receptors in chondrosarcoma cells is largely unknown. We found that the chondrosarcoma cells expressed EP1-4 receptors. However, EP1 but not other EP receptors was required for PGE
2-induced migration activity. Treatment with butaprost (EP2 agonist), and 11-deoxy-PGE1 (EP2/EP4 selective agonist) failed to up-regulate cell migration. Furthermore, EP1 but not EP3 siRNA inhibited PGE
2-induced cell migration. Therefore, our data suggest a critical role for EP1 receptor in the PGE
2-mediated cell migration in human chondrosarcoma cells.
Integrins link the extracellular matrix to intracellular cytoskeletal structures and signaling molecules and are implicated in the regulation of a number of cellular processes, including adhesion, signaling, motility, survival, gene expression, growth and differentiation [
3,
34]. Using flow cytometry analysis, we found that PGE
2 increased α2β1 but not α5, β3, α5β1 or αvβ3 integrin expression, which plays an important role during tumor metastasis. Furthermore, PGE
2 also increased the mRNA levels of α2 and β1 integrins. In addition, over-expression COX-2 increased the mRNA expression of α2 and β1 integrins. It has been often reported that α2β1 integrin has revealed the ability to act as critical molecules as regards metastasis the ability of chondrosarcoma cells [
35]. In addition, activation of α2β1 integrin intracellular signal increased migration activity of chondrosarcoma cells [
35]. Similarly, it was found that elevated expression of Cyr61 induced gastric cancer cell migration through α2β1 integrin [
36]. Kawashima et al., also reported that tumour necrosis factor alpha induced migration of osteosarcoma cells via α2β1 integrin [
37]. Collectively, our data also reveal that COX-2 and its downstream effector integrin α2β1, could constitute a potential target for future treatment of metastasis of chondrosarcoma cells.
It has been reported that PLC/PKC/c-Src dependent pathway is involved in EP1 receptor signaling [
28]. In present study, we found PGE
2 increased PLCβ3 phosphorylation in JJ012 cells. Several isoforms of PKC have been characterized at the molecular level and these have been found to mediate several cellular molecular responses [
38]. We demonstrated that PKC inhibitor GF109203X antagonized the PGE
2-mediated potentiation of migration activity and integrin expression, suggesting that PKC activation is an obligatory event in PGE
2-induced α2β1 integrin expression in these cells. This was further confirmed by the result that the dominant negative mutant of PKCα inhibited the enhancement of migration activity by PGE
2. Src, a tyrosin kinase, plays a critical role in the induction of chemokine transcription [
39]. In human aortic endothelial cells, oxidized phospholipids induce IL-8 expression through c-Src activation [
39]. As c-Src has been reported to be a downstream effector of G protein-coupled receptor [
40], we examined the potential role of c-Src in the signaling pathway of PGE
2-induced cell migration and integrin expression. We found that treatment of chondrsarcoma cells with PGE
2 induced increases in c-Src phosphorylation at Tyr416. Taken together, our results provide evidence that PGE
2 up-regulates cell migration and integrin expression in human chondrosarcoma cells via the EP1/PLC/PKCα/c-Src signaling pathway.
Methods
Materials
Anti-mouse and anti-rabbit IgG-conjugated horseradish peroxidase, rabbit polyclonal antibodies specific for PLCβ, PKCα, c-Src, IKK, p-IκBα, IκBα, p65 and the siRNAs against PLCβ and control (negative control for experiments using targeted siRNA transfection; each consisted of a scrambled sequence that would not lead to the specific degradation of any known cellular mRNA) were purchased from Santa Cruz Biotechnology (Santa Cruz, CA, USA). Rabbit polyclonal antibody specific for p-IKKα/β, p-PLCβ3, p-PKCα, p-c-Src and p-p65 were purchased from Cell Signaling and Neuroscience (Danvers, MA). Rabbit polyclonal antibodies specific for α2, α5, β3, αvβ3, α5β1 and α2β1 integrin were purchased from Chemicon (Temecula, CA). PGE
2, 17-phenyl trinor PGE
2, butaprost, sulprostone, 11-deoxy-PGE
1, SC19220 and rabbit polyclonal antibody specific for COX-2, EP1 and EP3 were purchased from Cayman Chemical (Ann Arbor, MI). Valeryl salicylate, NS398, U73122, GF109203X, PP2, PDTC, TPCK and IPTG (isopropyl-β-D-thiogalactopyranoside) were obtained from Calbiochem (San Diego, CA). Celebrex was obtained from Pharmacia Co. (Piscataway, NJ). ON-TARGET smart pool EP1 and EP3 siRNA and ON-TARGET plus siCONTROL Nontargeting pool siRNA were purchased from Dharmacon. The COX-2 IPTG-induced expression plasmid, p-NLR-COX2 was a gift from Dr. W.M. Fu (National Taiwan University) [
41]. The IKKα(KM) and IKKβ(KM) mutants were gifts from Dr. H. Nakano (Juntendo University, Tokyo, Japan). The PKCα dominant negative mutant was a gift from Dr. V. Martin (Louis Pasteur de Strasbourg University, France). The c-Src dominant negative mutant was a gift from Dr. S. Parsons (University of Virginia Health System, Charlottesville, VA). The NF-κB luciferase plasmid was purchased from Stratagene (La Jolla, CA) and luciferase assay kit was purchased from Promega (Madison, MA, USA). All other chemicals were obtained from Sigma-Aldrich (St. Louis, MO, USA).
Cell culture
The human chondrosarcoma cell line (JJ012) was kindly provided by the laboratory of Dr. Sean P Scully (University of Miami School of Medicine, Miami, FL, USA). The JJ012 cells were cultured in DMEM/α-MEM supplemented with 10% fetal bovine serum (FBS) and maintained at 37°C in a humidified atmosphere of 5% CO2. The human chondrosarcoma cell line (SW1353) was obtained from the American Type Culture Collection. The cells were cultured in DMEM/α-MEM supplemented with 10% FBS and maintained at 37°C in a humidified atmosphere of 5% CO2.
Migration assay
The migration assay was performed using Transwell (Costar, NY; pore size, 8-μm) in 24-well dishes. Before the migration assay was performed, cells were pretreated for 30 min with different concentrations of inhibitors, including the U73122, GF109203X, PP2, PDTC, TPCK or vehicle control (0.1% DMSO). Approximately 1×10
4 cells in 100 μl of serum-free medium were placed in the upper chamber, and 300 μl of the same medium containing PGE
2 was placed in the lower chamber. The plates were incubated for 24 h at 37°C in 5% CO
2, then cells were fixed in methanol for 15 min and stained with 0.05% crystal violet in PBS for 15 min. Cells on the upper side of the filters were removed with cotton-tipped swabs, and the filters were washed with PBS. Cells on the underside of the filters were examined and counted under a microscope. Each clone was plated in triplicate in each experiment, and each experiment was repeated at least three times. The number of migrating cells in each experiment was adjusted by the cell viability assay to correct for proliferation effects of the PGE
2 treatment (corrected migrating cell number = counted migrating cell number/percentage of viable cells) [
42].
Flow Cytometric Analysis
Human chondrosarcoma cells were plated in six-well dishes. The cells were then washed with PBS and detached with trypsin at 37°C. Cells were fixed for 10 min in PBS containing 1% paraformaldehyde. After rinsing in PBS, the cells were incubated with rabbit anti-human antibody against α2, α5, β3, αvβ3, α5β1 or α2β1 integrin (1:100) for 1 h at 4°C. Cells were then washed again and incubated with fluorescein isothiocyanate-conjugated goat anti-rabbit secondary IgG (1:150; Leinco Tec. Inc., St. Louis, MO, USA) for 45 min and analyzed by flow cytometry using FACS Calibur and CellQuest software (BD Biosciences, Palo Alto, CA, USA).
Western blot analysis
The cellular lysates were prepared as described previously [
43]. Proteins were resolved on SDS-PAGE and transferred to Immobilon polyvinyldifluoride (PVDF) membranes. The blots were blocked with 4% BSA for 1 hr at room temperature and then probed with rabbit anti-human antibodies against p-PLCβ3, p-PKCα, p-c-Src or p-p65 (1:1000) for 1 hr at room temperature. After three washes, the blots were subsequently incubated with a donkey anti-rabbit peroxidase-conjugated secondary antibody (1:1000) for 1 hr at room temperature. The blots were visualized by enhanced chemiluminescence using Kodak X-OMAT LS film (Eastman Kodak, Rochester, NY, USA).
PKC kinase activity assay
PKC activity was assessed by a PKC Kinase Activity Assay Kit according to manufacturer's instructions (Assay Designs, MI). The PKC activity kit is based on a solid-phase ELISA that uses a specific synthetic peptide as a substrate for PKC and a polyclonal antibody that recognized the phosphorylated form of the substrate.
Reporter assay
The chondrosarcoma cells were transfected with reporter plasmid using Lipofectamine 2000 (Invitrogen) according to the manufacturer's recommendations. Twenty-four hours after transfection, the cells were treated with inhibitors for 30 min, and then PGE
2 or vehicle was added for another 24 hr. Cell extracts were then prepared, and luciferase and β-galactosidase activities were measured [
42,
44].
Quantitative real time PCR
Total RNA was extracted from cancer cells using a TRIzol kit (MDBio, Taipei, Taiwan). The reverse transcription reaction was performed using 2 μg of total RNA that was reversely transcribed into complementary DNA using oligo(dT) primer. The quantitative real time PCR (qPCR) analysis was carried out using a Taqman® one-step PCR Master Mix (Applied Biosystems, CA, USA). One hundred ng of total cDNA were added per 25-μl reaction with sequence-specific primers and Taqman® probes. Sequences for all target gene primers and probes were purchased commercially [GAPDH was used as internal control (Applied Biosystems, CA, USA)]. qPCR assays were carried out in triplicate with an StepOnePlus sequence detection system. The cycling conditions were 10-min polymerase activation at 95°C followed by 40 cycles at 95 °C for 15 s and 60 °C for 60 s. The threshold was set above the non-template control background and within the linear phase of target gene amplification in order to calculate the cycle number at which the transcript was detected (denoted CT).
Patients and specimen preparation
Upon approval by the local ethics committee, specimens of tumor tissue or normal cartilage tissue were obtained from patients, who had been pathologically diagnosed with chondrosarcoma or knee osteoarthritis (the articular cartilage was collected) and had undergone surgical resection at the China Medical University Hospital. The chondrosarcoma patient group consisted of 6 females and 11 males and ranged in age from 22 to 68 years (mean, 48 years). The histologic grade of chondrosarcoma was checked. Cytologically, increased cellularity and cytological atypia are the most important features, and these characteristics are used to determine the grade of the chondrosarcoma [
45]. Eleven patients were alive without disease, one was alive with disease, two died without disease, and three died of causes secondary to progressive disease. The overall survival estimate at 5 years was 90%. The recurrence rate for patients with adequate surgical margins was 10%, compared with 75% for patients with inadequate margins. Tissue specimens were ground and then sonicated in a TRIzol kit. The mRNA level was analyzed using qPCR analysis.
For primary cultures from human chondrosarcoma cells, the samples were cleaned of surrounding fat, connective tissue and blood vessels. Thereafter, tissue samples were minced into pieces using a razor blade. Minced samples were transferred into 50 ml Falcon tubes, spun down at 1000 r.p.m. for 5 min and rinsed twice with fresh PBS. Digestion was performed with 1 mg collagenase II/ml PBS at 37°C for 50 min in a shaking water bath. Cell suspension was pipetted up and down at least twice during incubation. After digestion, pure FBS was added to a minimum concentration of 10% to inactivate the collagenase, followed by a centrifugation step as described above. Cells were then cultured in Dulbecco's modified Eagle's medium/α-modified Eagle medium supplemented with 10% FBS and maintained at 37°C in a humidified atmosphere of 5% CO
2[
46].
Primary cultures of human chondrocytes were isolated from articular cartilage as described previously [
47]. The cells were grown in plastic cell culture dishes in 95% air-5% CO2 with Dulbecco's modified Eagle's medium which was supplemented with 10% FBS, 2 mM-glutamine, penicillin (100 U/ml) and streptomycin (100 μg/ml).
Statistics
The values given are means ± S.E.M. The significance of difference between the experimental groups and controls was assessed by Student's t test. The difference was considered significant if the p value was < 0.05.
Competing interests
The authors declare that they have no competing interests.
Authors' contributions
Conceived and designed the experiments: CT
Performed the experiments: JL, YF and CC
Analyzed the data and provided the suggests: CHu, HC, WY, CHs and LJ.
All authors read and approved the final manuscript.