Effect of Aspirin on Cell Growth of Human MG-63 Osteosarcoma Line

Nonsteroidal anti-inflammatory drugs (NSAIDs) are commonly used in bone tissue repair treatment for their pharmacological action. The objective of this study was to determine the effect of aspirin, on osteoblast growth, using MG63 cell line as osteoblast model. MTT spectrophotometry results showed that 20, 100, and 1000 μM aspirin doses have an inhibitory effect on growth. Cell cycle analysis revealed that aspirin doses of 100 and 1000 μM arrest the cell cycle in phase GO/G1. Parallel apoptosis/necrosis studies showed no changes in comparison to control cells after treatment with 1 or 10 μM aspirin but a significantly increased percentage of cells in apoptosis at doses of 20, 100, and 1000 μM. We highlight that treatment of osteoblast-like cells with 1000 μM aspirin increased not only the percentage of cells in apoptosis but also the percentage of necrotic cells, which was not observed in aspirin treatments at lower doses.


Introduction
Nonsteroidal anti-inflammatory drugs (NSAIDs) are widely used in orthopaedic surgery and traumatology to reduce pain and inflammation. Animal and cell culture studies have shown that some NSAIDs have an adverse effect on bone tissue through regeneration delay [1][2][3][4][5][6].
The mechanism by which NSAIDs exert their action on cell growth is under debate. Some authors cite the capacity of NSAIDs to inhibit synthesis of prostaglandin (PG), a molecule that is synthesized by osteoblasts and autocrinally favours their growth [7,8]. Others propose that the drug has a direct effect on the cell cycle based on in vitro findings that therapeutic doses of ketorolac, indomethacin, or diclofenac induce cell death in osteoblast cultures from rat foetal calvaria and may suppress bone formation and impair bone remodelling by arresting cell cycle in phase G 0 /G 1 [9,10].
Different NSAIDs were recently reported to affect osteoblast proliferative capacity and modulate other features of this cell population, including differentiation, antigenic profile, and phagocytic capacity [11,12]. However, Arpornmaeklong et al. [13] found that indomethacin and celecoxib inhibit cell growth but have a less clear effect on cell differentiation as determined by alkaline phosphatase and osteocalcin synthesis.
Acetylsalicylic acid (aspirin) is very frequently administered for its anti-inflammatory, antipyretic, antiaggregant, and analgesic properties. However, in contrast to other NSAIDs, few data are available on its effects on bone tissue or on osteoblasts, the cells responsible for bone formation and regeneration. Therefore, the objective of this study was to analyse the effect of aspirin at different doses on osteoblast cell growth, using the human MG63 osteosarcoma cell line. Cells were detached from the culture flask with a solution of 0.05% trypsin (Sigma) and 0.02% ethylene diamine tetraacetic acid (EDTA) (Sigma) and then washed and suspended in complete culture medium with 10% FBS.

Cell Proliferation.
Cell proliferation was determined by the MTT method. Osteoblasts were seeded at 1 × 10 4 cells/mL per well into a 96-well plate without FBS and cultured at 37 • C for 24 hours. Subsequently, the medium was replaced with DMEM containing aspirin at a dose of 0, 0.1, 1, 10, 20, 100, or 1000 μM. At the end of treatments, the medium was replaced with DMEM containing 0.5 mg/mL MTT (Sigma) and incubated for 4 hours. Cellular reduction of the MTT tetrazolium ring resulted in the formation of a dark-purple water-insoluble deposit of formazan crystals. After incubation, the medium was aspirated and DMSO was added to dissolve the formazan crystals. Absorbance was measured at 570 nm with a spectrophotometer (Sunrise, Tecan, Männedorf, Switzerland).

Cell Cycle.
Cultured human MG-63 osteosarcoma cells treated with 1, 10, 20, 100, or 1000 μM of aspirin and untreated control cells were detached from the culture flask by treatment with a solution of 0.05% trypsin (Sigma) and 0.02% EDTA (Sigma) and subsequently washed, and suspended in PBS and prepared for the study of cell cycle as reported by García-Martínez et al. [15]. The suspension obtained was placed in 200 μL PBS with 2 mL ice-cold 70% ethanol and 30% distilled H 2 O and then vigorously mixed. Cells were left for at least 30 min. in the cold and then harvested by centrifugation and resuspended in 800 μL PBS. Cells were microscopically examined and, if clumped, passed through a 25-gauge syringe needle. Cells were then incubated at 37 • C for 30 min. with 100 μL ribonuclease (RNase) (1 mg/mL) and 100 μL propidium iodide (PI). Finally, samples were analyzed by using an argon-ion laser tuned to 488 nm (Fasc Vantage Becton Dickinson), measuring forward and orthogonal light scatter and red fluorescence, determining both area and Esther peak of the fluorescent signal. were included, we calculated the percentage of annexinpositive (apoptotic) cells and PI-positive (necrotic) cells from 2000-3000 cell counts.

Statistical
Analysis. R software (version 2.9.2, Auckland, New Zealand) was used for data analysis. Mean values (±standard deviation) were calculated for each variable. A two-way repeated-measures analysis of variance (ANOVA) was performed to examine the effects on proliferation, cell cycle, and apoptosis/necrosis induction, considering treatment (aspirin), time (24 h), and concentration (0.1, 1, 10, 20, 100, or 1000 μM). When a significant interaction was identified, the Bonferroni correction was applied for planned pair-wise comparisons. P < 0.05 was considered significant. At least three experiments were performed for each culture.

Discussion
The anti-inflammatory properties of NSAIDs, including aspirin, derive from their powerful inhibitory effects on cyclooxygenase metabolites such as prostaglandin E2 [16]. Consequently, some authors attribute the adverse effect 4 The Scientific World Journal of NSAIDs on osteoblasts to a reduced synthesis of prostaglandins, which act as bone cell growth factors, as a result of the inhibition of cyclooxygenase enzymes [17]. However, there is some controversy concerning the adverse effect of NSAIDs on osteoblast growth [10,18]. The disparate results obtained may be due to multiple factors, including dosage, treatment duration, and the species in question [13,17]. In this study, the proliferative capacity of cells from the MG-63 cell line was not significantly inhibited by 24 h treatment with 0.1, 1, or 10 μM aspirin but was significantly inhibited by 24 h treatment with 20, 100, and 1000 μM aspirin. Therefore, this NSAID does not have an adverse effect on bone cell proliferation in vitro at the therapeutic dose range used in the clinical setting (1 to 10 μM). It was previously reported that the dose of NSAIDs is a key factor in the effect on cell proliferation as well as on cell differentiation and migration [19].
The effect of different doses on the growth of the MG63 line is closely related to the effects observed on the cell cycle. Thus, the negative effect on growth at 100 and 1000 μM aspirin may be explained by the significant increase in the percentage of cells in phase G0/G1 versus the control group. Ann V and PI staining showed that the reduced cell growth at 20 and 100 μM doses was attributable to apoptosis rather than necrosis. In contrast, treatment with a 1000 μM produced an increase in necrotic cells as well as cells in apoptosis.
We highlight that treatment of the MG63 line with therapeutic doses of aspirin (1-10 μM) did not cause cell death, cell cycle changes, or modifications in apoptosis/necrosis induction. In contrast, therapeutic doses of ketorolac, indomethacin, or diclofenac induced cell death in osteoblast cultures from rat foetal calvaria and may suppress bone formation and impair bone remodelling by cell cycle arrest in G 0 /G 1 phase [9,10]. In another in vitro study, 24 h treatment with indomethacin or nimesulide at therapeutic doses also reduced osteoblast growth capacity and produced significant changes in the cell cycle, which was again arrested in G 0 /G 1 phase [12].
A recent cohort study of subjects exposed and not exposed to NSAIDs and opioids observed no difference in bone mineral density over time but reported excessive risk of fractures in users of some NSAIDs, although not in those receiving aspirin [20]. These results are consistent with the present in vitro data.
Furthermore, another important aspect of aspirin, from a clinical standpoint, is that when the lipoxin pathway 5 is activated in the presence of aspirin, acetylation of the cyclooxygenase 2 enzyme present at inflammation sites not only inhibits further production of prostanoids, but also induces the synthesis of 15-hydroxyeicosatetraenoic acid, which is then transformed into 5(S)-epoxytetraene in leukocytes in the presence of 5-lipoxygenase. The 5(S)epoxytetraene intermediate is then transformed to 15epilipoxins or aspirin-triggered lipoxins, which are more bioactive than native lipoxins and have more powerful resolving properties [21,22].
In conclusion, aspirin at therapeutic doses appears to have no adverse effect on osteoblast growth, unlike some other NSAIDs. Growth was only reduced at higher doses, by cell cycle arrest and apoptosis induction. These findings support the use of aspirin in the treatment of inflammation and pain in bone lesions requiring tissue regeneration. Given reports that indomethacin and diclofenac can increase cell adhesion and reduce the migration of different cell populations [23][24][25], further research is warranted to determine whether aspirin may exert action on the cell adhesion or migration of osteoblasts, other key factors in the regenerative process.