- Open Access
IL-1 does not reverse the anti-proliferative effect of aspirin in breast cancer cells
© Sali and Jewell; licensee BioMed Central Ltd. 2006
- Received: 10 February 2006
- Accepted: 04 September 2006
- Published: 04 September 2006
Interleukin- 1 (IL-1) is a multifunctional proinflammatory cytokine. There have been studies suggesting a role in affecting growth and invasiveness of malignant breast cells by either blocking or stimulating growth of cultured MCF-7 breast cancer cells. This effect may be mediated by induction of COX-2. Aspirin is an inhibitor of COX-2 and has been implicated, with other non-steroidal anti-inflammatory drugs (NSAIDS) in prevention and treatment of breast cancer. In this study the in vitro effects of IL-1 and aspirin on growth of MCF-7 human breast cancer cells was examined.
MCF-7 cells were treated with various concentrations of IL-1 and aspirin alone and in combination. Cell growth was assessed by cell number measurement.
Aspirin significantly decreased growth rate in a dose-dependant manner, alone and as a combined treatment with IL-1 with a maximum reduction in growth rate at 300 mg/ml (P < 0.05). Treatment with IL-1 alone showed no significant effect on growth rate of MCF-7 cells (P > 0.05).
This study confirms that aspirin suppresses the proliferation rate of MCF-7 cells both as a single agent and in combination with IL-1. It also suggests that IL-1 alone does not stimulate or inhibit growth of MCF-7 cells.
- Breast Cancer
- Breast Cancer Cell
- Breast Cancer Cell Line
- Insulin Growth Factor Receptor
Interleukin-1 (IL-1) is a pro-inflammatory cytokine affecting many cell types [1, 2]. IL-1 is also present in high levels at tumor sites where it has been shown to have effects on the growth and invasiveness of malignant cells by either inducing growth factors that promote carcinogenesis and tumor metastasis , or by decreasing tumor growth by direct cytotoxic action . It is thought that expression of high levels of IL-1 cause broad inflammation which damages tissue and therefore tumor invasiveness is induced [1, 3]. In addition, IL-1 induce the expression of pro-inflammatory enzymes mainly Cyclooxygenase 2 (COX-2), inducible nitric oxide (iNOS), as well as other cytokines and chemokines. There is also evidence that IL-1 is secreted by various human tumor cells and in most cases increases invasive patterns in the tumor cells; antitumor effects were rarely observed . 90% of invasive breast cancers showed IL-1 expression but to a lesser extent in benign tumors. Furthermore high levels of IL-1 were associated with other parameters of aggressive tumors such as estrogen receptor negativity and p53 gene mutations .
Cyclooxygenase (COX) is an enzyme that catalyses the conversion of arachidonic acid to important biological mediators known as prostanoids (prostaglandins, thromboxanes and prostacyclin) [5, 6]. COX-2 is an inducible form which is not detected in most healthy tissues but can be induced in response to a variety of stimuli such as proinflammatory cytokines (TNF, IL-1), hormones, bacterial polysaccharides and growth factors [5, 7, 8]. Studies over recent years have suggested an important role of COX-2 in tumor formation and progression. Various human malignancies including breast cancer have shown increased expression of COX-2. In one study, intermediate or high levels of COX-2 were detected in 43% of Human Breast cancer carcinomas and in 62.5% of Ductal Carcinoma in Situ, and also COX-2 expression was found in MCF-7 breast cancer cell line induced by HER2 and no COX-2 proteins in MCF-7 cells alone . Davies et al also detected COX-2 protein expression in 63 of 89 breast tumors using immunohistochemical analysis . Costa and colleagues revealed that COX-2 was expressed in 17.4% of breast carcinomas studied, analyzed by both immunohistochemistry and western blotting and that COX-2 was not detected in normal breast tissue. The study also showed that COX-2 expression was associated with angiogenesis, lymph node metastasis and apoptosis in human breast cancer .
NSAIDs are widely used in treating symptoms such as pain and fever associated with inflammation. Epidemiological studies report that these drugs particularly aspirin may be associated with reduced risk of cancer development. Some studies have focused on reduced incidence of colorectal cancer with NSAIDs use , while others have related to breast cancer. One large prospective cohort study by Johnson et al reported a trend of decreasing risk of incident breast cancer among postmenopausal women with frequent use of aspirin but not with other NSAIDs . Another case-control study suggested a 40% reduction in breast cancer incidence in women who reported daily intake of aspirin and other NSAIDs for at least ten years . However some studies found no difference in aspirin intake among women who developed breast cancer and those who did not . The main target of NSAIDs is the COX enzyme and acts by efficiently blocking its activity and thus inhibiting COX2. This therefore inhibits production of several prostaglandins which when elevated may promote carcinogenesis, through increased cell proliferation, immune suppression, tumour promotion and facilitate metastasis . Inhibitory effects by certain COX-2 inhibitors on growth in cancer cell lines have been shown in some studies. DFU, [5,5-dimethyl-3-(3-fluorophenyl)-4-(4-methylsulphonyl)phenyl-2(5H)-furanone], a selective COX-2 inhibitor was found to significantly reduce tumour growth in mice injected with MCF-7 cells and also inhibited growth when MCF-7 cells were cultured for a long period at high drug concentrations . A study by Goel et al found that aspirin inhibited growth in three colon cancer cell lines . Aspirin and its parental compound acetylsalicylic acid causes irreversible inactivation of COX enzyme acting on both COX-1 and -2. In addition to its anti-inflammatory action, aspirin has been known to have anti-proliferative effects as well as anti-apoptotic effects on cancer. This study, therefore aimed to investigate the interactions between the pro-inflammatory cytokine IL-1 and anti-inflammatory aspirin on MCF-7 breast cancer cells.
MCF-7 cells were cultured in DMEM with 10% foetal calf serum. Cells were trypsinized, and 2.0 × 105 cells/ml plated per well in multi well plates. After incubation for twenty four hours, the cells in ten wells from each plate were treated in duplicate with different concentrations of IL-1 or aspirin alone and in combination. Viable cells were counted at 48, 72, 120 and 168 hours and results recorded. Results were analyzed by one-way analysis of variance test (ANOVA).
Aspirin inhibited growth of human breast cancer cell line MCF-7
No effect of IL-1 on growth of MCF-7 cell line
No effect of IL-1 on aspirin-mediated inhibition of proliferation of MCF-7 cells
MCF-7 breast cancer cells were exposed to 5 ng/ml IL-1 followed by three concentrations of aspirin, incubated and viable cells counted for a period of 72 hours. At 300 mg/ml aspirin, a significant reduction in proliferation rate of about 70% was observed (p < 0.05) compared to the control group, and was also significantly different from the other treatment concentrations after 72 hours (Figure 3). Maximal effect of aspirin inhibition was observed after 120 hours at a dose of 300 mg/ml (p < 0.05). Significant inhibition effects were also seen at 3 mg/ml and 30 mg/ml after 120 hours (p < 0.05).
These findings suggest that aspirin is capable of inhibiting growth rate of MCF-7 cells even when combined with IL-1.
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