The antiproliferative effect of C2-ceramide on lung cancer cells through apoptosis by inhibiting Akt and NFκB
- I-Ling Lin†1,
- Han-Lin Chou†2, 6,
- Jin-Ching Lee2,
- Feng-Wei Chen2,
- Yao Fong3,
- Wei-Chiao Chang4,
- Hurng Wern Huang5,
- Chang-Yi Wu6,
- Wen-Tsan Chang7,
- Hui-Min David Wang8 and
- Chien-Chih Chiu1, 2Email author
© Lin et al.; licensee BioMed Central Ltd. 2014
Received: 27 June 2013
Accepted: 23 December 2013
Published: 6 January 2014
The anticancer effects of ceramide have been reported in many types of cancers but less in lung cancer. In this study, we used C2-ceramide to further investigate its possible anticancer effects and mechanisms on non-small cell lung cancer (NSCLC) H1299 cells. The result of cell proliferation in terms of trypan blue assay showed high dose of C2-ceramide inhibited cell survival after 24 h treatment. The flow cytometry-based assays indicated the effect of apoptosis, chromatin condensation, and G1 arrest in terms of Annexin V/propidium iodide (PI), DAPI, and PI stainings, respectively. Moreover, the decreased protein level of p-Akt, p-NFκB, survivin and cyclin A2 were detected by Western blot assay. Taken together, these results indicated the antiproliferative effect of C2-ceramide is majorly responsible for cell apoptosis in lung cancer H1299 cells.
Approximately 80% of lung cancer belongs to non-small-cell lung cancer (NSCLC) and the other is SCLC histologically. Although smoking is one of the main risk factors for lung cancer, about 10% patients are non-smokers. NSCLC is generally detected and diagnosed at late stage and its prognosis is poor. Therefore, the anticancer drugs for NSCLC treatment remain a challenge.
Akt, a serine/threonine kinase, regulates cell growth, cell cycle progression, survival and anti-apoptosis. Dysregulation of Akt was reported to be observed in various cancers including breast cancer and lung cancer cells. Furthermore, the constitutive activation of Akt has been shown to cause chemoresistant of cancer cells. Similarly, NFκB, an inflammatory-associated transcription factor, is also found to be constitutively activated or aberrantly expressed in lung cancer[7, 8]. Therefore, targeting of Akt and NFκB signaling seems to be a promising strategy for lung cancer therapy[9–12].
Ceramides are important components composed of lipid molecules and can form into sphingolipids when added functional groups on their hydroxyl group such as phosphate choline or monosaccharide. When cells are triggered by certain stimuli, an enzyme called sphingomyelinase would hydrolyze sphingolipids and cause the release of ceramides into cytoplasm, which can undergo many biological processes, such as differentiation, proliferation, growth arrest and apoptosis. Ceramide was reported to act as an important mediator in apoptosis pathways. Exogenous ceramides have been demonstrated to induce anti-proliferation and apoptosis in many cancers. Furthermore, accumulating evidence showed that ceramide inhibits proliferation of cancer cells via inhibiting Akt and NFκB signal pathways[16, 17].
The ceramide-mediated anticancer effects have been reported in many types of cancers such as pancreatic, breast, gastric, hematologic cancer. However, the final outcome of ceramide treatment may depend on the context of cell types. Previous studies showed that knockout of NFκB p65 sensitizes embryonic fibroblasts toward C2-ceramide induced cell death. On the contrary, the above study also found that C2-ceramide induces cell death and activation of NFκB in lung cancer H1299 cells. The effects of C2-ceramide on apoptosis of H1299 cells were investigated previously[22, 23]. In the current study, we examined the growth inhibitory property to NSCLC H1299 cells by C2-ceramide as well as its possible apoptosis mechanism, especially inhibiting Akt and NFκB pathways.
Materials and methods
The H1299 lung cancer cells were maintained in DMEM medium (Invitrogen, Carlsbad, CA USA) containing 10% fetal bovine serum (FBS), 100 U/ml penicillin, 100 μg/ml streptomycin, 0.03% glutamine and 1 mM sodium pyruvate and kept at 37°C in a humidified atmosphere with 5% CO2.
Cell survival assay
Cell survival was determined by the trypan blue dye exclusion assay as previously described[25, 26]. In brief, Cells were seeded at a density of 1 × 105 cells per well. After 24 h of incubation, the cells were treated with C2-ceramide (#A7191, Sigma) at concentrations of 0, 10, 20, and 50 μM for 24 h, then 0.2% trypan blue were added to wells. Finally, the viable cells we are calculated by the Countess® Automated Cell Counter (Invitrogen, Diego, CA, USA). The assay was triplicated and the IC50 was calculated by the slope and intercept accordingly to two concentrations of C2-ceramide between the half-maximal proliferative inhibition.
Apoptosis was detected by annexin/PI staining (Pharmingen, San Diego, CA, USA) as previously described. Briefly, cells were treated with C2-ceramide at concentrations of 0, 10, 20, and 50 μM for 24 h. After collection, cells were treated with 10 μg/ml of annexin V-fluorescein isothiocyanate and 5 μg/ml of PI for analysis with a FACSCalibur™ flow cytometer (Becton-Dickinson).
Chromatin condensation assay
5 × 105 H1299 cells were seeded onto a 6-well plate. After 24 h, cells were treated with indicated concentrations (0 to 50 μM) of ceramide for 24 h. After wards, cells were stained with 5 μg/ml of DAPI for 3 mins at 37°C. The level of chromatin condensation was determined by a flow cytometry (Becton-Dickinson). At least 10,000 stained cells were counted and calculated as percentage of chromatin condensation compared to those of the control cells.
Cell cycle distribution
Propidium iodide (PI, Sigma, St. Louis, MO, USA) staining for DNA content measurement was performed as described previously. Briefly, cells were treated with 0, 10, 20, and 50 μM of C2-ceramide for 24 h. After collection, cells were washed twice with PBS before 70% ethanol fixation. After centrifugation, the cells were incubated with 10 μg/ml PI and 10 μg/ml RNase A in PBS for 15 min at room temperature in the dark. Cell cycle analyses were performed using a FACSCalibur flowcytometer (Becton-Dickinson, Mansfield, MA, USA).
Western blot assay was performed as described previously. Briefly, cells were collected for lysate preparation. After centrifugation, and protein concentrations of lysates were determined. Protein lysates for 40 μg were loaded and electrophoresed by 10% SDS-polyacrylamide gel (PAGE) and then transferred to membrane. The membranes were blocked with 5% non-fat milk. Subsequently, it was reacted with primary antibodies against t-Akt (#1081), p-NFκB (Ser536, #2220) and Bax (#1063, Epitomics, CA, USA); t-NFκB (sc-8008), β-catenin (sc-7963) and p-Akt (Ser473, sc-7985, Santa Cruz Biotech, Santa Cruz, CA, USA); Cyclin A2 (GeneTex Co., Cat No. GTX103042); survivin (AnaSpec, San Jose, CA, USA) and β-actin (#sc-8432, Santa Cruz Biotech), and their corresponding secondary antibodies. The ECL™ (Amersham Piscataway, NJ, USA) chemiluminescence detection kit was applied.
All data are presented as mean ± S.D. Comparison between experimental groups and vehicle controls was assessed by one-way ANOVA test.
Anti-proliferative effects of C2-Ceramide-Treated H1299 lung cancer cells
G1 arrest of C2-Ceramide-treated H1299 lung cancer cells
Apoptosis induction of C2-Ceramide-treated H1299 lung cancer cells
Chromatin condensation of C2-Ceramide-treated H1299 lung cancer cells
Modulation of p-Akt and p-NFκB in C2-Ceramide-treated H1299 lung cancer cells
The modulations of ceramide as the strategy for many kinds of cancer therapies have been reported[18–21]. For example, acid ceramidase was regarded as the target for breast cancer therapy because it can hydrolyze ceramide, and thus reduce its intracellular levels. Previous study showed that C2-ceramide is not very harmful to normal cells. For example, the IC50 (24 h) of human dermal neonatal fibroblast (HDNF) cells for C2-ceramide was 66.5 μM, suggesting the moderately selective anti-proliferative effect of C2-ceramide toward cancer cells. In the current study, we found that the C2-ceramide induced apoptosis of H1299 lung cancer cells. It provides the idea that pharmacological modulation of sphingolipid metabolism can enrich the tumor cell ceramide for cancer chemotherapy.
Sometimes the degree of the sub-G1 accumulation may not appear in concert with the apoptosis in terms of Annexin V/PI staining. For example, no sub-G1 accumulation was found in C2-ceramide-treated H1299 lung cancer cells at 24 h treatment, but it still showed the apoptosis-inducible effects in terms of Annexin V/PI and DAPI-based chromatin condensation assays using flow cytometry. Similarly, (-)-Anonaine inhibits growth of H1299 cells without sub-G1 accumulation before 48 h incubation, however, the (-)-Anonaine ends up increasing apoptosis at 72 h treatment. Therefore, the absence of sub-G1 accumulation in C2-ceramide-treated H1299 at 24 h treatment may be due to the detection timing. Furthermore, chromatin condensation was thought to be one of hallmarks in apoptotic cells[32, 33]. However, some study indicated that certain stresses such as heat shock may induce a non-apoptotic chromosome condensation. For example, Plehn-Dujowich’s work found the non-apoptotic chromatin condensation. Accordingly, in our study, the non-apoptosis inducing dose of 20 μM C2-ceramide caused stress-induced chromatin condensation, which may explain the reason that C2-ceramide induces anti-proliferation without apoptosis (Figure 4). Eventually, a higher dose of 50 μM C2-ceramide causes the apoptotic chromatin condensation, resulting in cell death of H1299 cells.
This study was financially supported by grants NSC101-2313-B-037-001, NSC101-2622-B-037-002-CC3 and NSC101-2320-B-037-046-MY3 from the National Science Council, Taiwan; by grant 101-CM-KMU-11 from ChiMei-KMU Joint Research Project; and by grant #NSYSUKMU 102–28 from the NSYSU-KMU Joint Research Project. The authors thank the help from the Statistical Analysis Laboratory, Department of Medical Research, Kaohsiung Medical University Hospital, Kaohsiung Medical University, Taiwan.
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