- Primary research
- Open Access
PI3-kinase inhibition synergistically promoted the anti-tumor effect of lupeol in hepatocellular carcinoma
© Liu et al.; licensee BioMed Central Ltd. 2013
- Received: 20 June 2013
- Accepted: 28 October 2013
- Published: 1 November 2013
Lup-20(29)-en-3H-ol (Lupeol), a dietary triterpene, has been shown to possess multiple pharmacological activities including anti-tumor effects
In the current study, we noted that low doses of lupeol (<40 μM) promoted the growth of hepatocellular carcinoma (HCC) cells with a significant activation of the PI3-kinase/Akt signaling pathway. We further investigated the combined anti-tumor effect of lupeol and S14161, a newly identified PI3-Kinase inhibitor in vitro and in vivo
The results demonstrated that lupeol and S14161 could exert a synergistic antitumor effect resulting in chemo-sensitization of HCC to low doses of lupeol. Using an in vivo HCC model, we further demonstrated that lupeol and S14161 synergistically inhibited tumor growth without any adverse effects on body weight
Our studies showed that the activation of PI3-kinase/Akt pathway resulted in the tumor-promoting effect with low doses of lupeol. Combining PI3-kinase inhibitor with lupeol could synergistically augment the anti-tumor effect of lupeol and might be an applicable strategy for HCC therapy.
- Hepatocellular carcinoma
- PI3-kinase/Akt signaling
Hepatocellular carcinoma (HCC) becomes the fifth most frequent cancer and the third most common cause of cancer-related mortality in the world, preceded only by lung cancer and stomach cancer [1–4]. Asian countries account for nearly 78% of the roughly 600,000 cases of HCC reported globally each year . Although the prognosis of patients with HCC has marginally improved, a historical 5-year survival rate worldwide is still less than 5%, mainly because of a high potential for vascular invasion, metastasis, and recurrence even after surgical resection . Various approaches have been developed, curative effect is far from perfect due to the highly chemoresistant nature of the tumor and the toxicity of chemotherapeutic agents [4, 7–11]. Therefore, efforts are urgently needed to explore more effective therapeutic agents for treating HCC.
There is a growing interest in dietary substances obtained from natural products because of their minimal toxicity. Emphasis has been placed on triterpenes, due to their wide spectrum of biological activities. They could selectively or preferentially eliminate cancer cells by inhibiting cell cycle progression and by causing apoptosis . One such triterpene which has gained wide attention is lupeol [Lup-20(29)-en-3β-ol]. Extensive research over the last three decades has revealed various important pharmacological activities of lupeol under in vitro and in vivo conditions, including anti-inflammation, anti-arthritis, anti-diabetes, anti-heart diseases, anti-renal toxicity, anti-hepatic toxicity and anti-cancer [13–15]. Lupeol has been reported not only to induce differentiation and inhibit the growth of melanoma and leukemia cells [16–19], but also to inhibit tumor promotion in two-stage mouse skin carcinogenesis through modulating NF-κB and PI3-kinase (PI3K)/Akt pathways , and to inhibit growth and induce apoptosis in both prostate  and pancreatic cancers . Recent studies have also shown that lupeol induced apoptosis of HCC cells SMMC7721 by down-regulating death receptor 3 (DR3) , and also had in vivo and in vitro therapeutic effect for HCC by targeting liver tumor-initiating cells (T-ICs) through modulating PTEN-Akt-ABCG2 pathway . Our previous work also proved anti-HCC efficacy of lupeol and a combined effect with rTRAIL in inducing chemo-sensitization of HCC . Meanwhile, lupeol exhibited very low toxicity. Lupeol administered orally in a dose of 2 g/kg body weight has been reported to produce no adverse effects in rats and mice . However, the toxicity has not been examined in human. On the other hand, our previous results  showed that lupeol could also reduce the cell viability of the normal human liver cells with an IC50 of 90 μmol/L, suggesting that lupeol could exert toxic effect on normal cells. Lupeol concentrations of less than 30 μmol/L do not affect the normal liver cell viability. Lupeol has also been shown by numerous studies to have anti-inflammatory activity in rats and mice at the dose of 25-200 mg/kg [26–28]. Therefore, high doses of lupeol could also inhibit anti-tumor immune responses. Therefore, low dose of lupeol is desirable because it can minimize the toxicity to normal cells and the immune suppressive effect of lupeol if the anti-tumor effect could also be achieved. In the current study, we found that low doses of lupeol could promote tumor growth in vitro and had a very minimal effect on HCC in vivo. We further exploited the underlying mechanisms and demonstrated a synergistic effect of combination treatment with low doses of lupeol and PI3K inhibitor in HCC, which made low dose lupeol possible for tumor treatment.
PI3K/Akt pathway plays an important role in various types of cancers, including HCC. Akt is important in protecting the cells from various types of apoptotic stimuli and regulating cell proliferation and cell cycle by interacting, either directly or indirectly, with numerous other regulatory proteins [29, 30]. Blockage of Akt signaling by some reagents results in programmed cell death and growth inhibition of tumor cells [31–34]. Therefore, targeted therapies against specific components of this pathway are expected to be efficacious as single agents or in combination in a variety of human cancers. Up to now, many inhibitors of PI3K/Akt pathway have been developed. LY294002 and wortmannin both target the catalytic site p110 of PI3K. Due to their unfavorable pharmaceutical properties, toxicity, and crossover inhibition of other lipid and protein kinases, they were not extensively used in clinical trials . Recently, 8-ethoxy-2-(4-fluorophenyl)3-nitro-2H-chromene (S14161) showed potent anti-leukemia and anti-myeloma activity in vitro and inhibited in vivo tumor growth . S14161 has been shown to have no effect on the cell viability of the normal hematopoietic cells with the concentration as high as 25 μmol/L and no effect on body weight with 100 mg/kg/day intraperitoneal injection for 10 days. The effect of S14161 on HCC has not been determined.
In the present study, we unexpectedly discovered that low doses of lupeol promoted cell growth of HCC cells through the activation of PI3K/Akt pathway. To further improve the anti-tumor efficacy of lupeol, we combined lupeol treatment with S14161. The results demonstrated that lupeol and S14161 could exert synergistic effects inhibiting tumor growth in vitro and in vivo. Our results provided evidence that PI3-kinase/Akt signaling pathway activation promoted tumor growth by low doses of lupeol. Combining PI3K inhibition and lupeol treatment could provide safer and more effective anti-tumor therapeutic regimen.
Cell lines and culture
Human HCC cell lines, HepG2 and SMMC7721, were purchased from Cell Bank, Chinese Academy of Sciences (Shanghai, China). They were maintained in Dulbecco’s modified Eagle’s medium (DMEM) with high glucose (Gibco BRL, Grand Island, NY) supplemented with 10% heat-inactivated fetal bovine serum (Gibco BRL, Grand Island, NY), 10mg/ml penicillin G and 50 μg/ml treptomycin (Shanghai Sangon Biological Engineering Technology & Services Co., Shanghai, China) at 37°C in a humidified atmosphere containing 5% CO2. Cells were harvested using 0.25% trypsin/EDTA (Invitrogen, Carlsbad, CA).
Antibodies and reagents
Lupeol was purchased from Sigma-Aldrich (St. Louis, MO) and a stock solution of lupeol (30 mmol/L) was prepared by resuspension in warm alcohol and dilution in DMSO at 1:1 ratio.
Antibodies against β-actin was purchased from BD Pharmingen (Franklin Lakes, NJ). Antibodies against PI3/K p110δ, phospho-Akt (Thr308) and total-Akt were purchased from Cell Signal Technology (Boston, MA). Cytoplasmic Protein Extraction Kit and BCA Protein Assay Kit were purchased from Beyotime (Nantong, China).
Cell viability assay
The effect of Lupeol and/or S14161 on cell viability was determined by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromide (MTT) assay. Cells were plated at 3 × 103 per well in 100 μl of complete culture medium in 96-well cell culture plates 24 h before the assay. Then cells were treated with different concentrations of related compounds for 48 h. Each concentration was repeated in 5 wells. After incubation for 48 h, 20 μl MTT (5 mg/ml in PBS) was added to each well and incubated for 4 h; then the medium was removed, 0.1 mL of buffered DMSO was added to each well. The absorbance was recorded on a microplate reader at the wavelength of 490 nm. The effect on cell growth inhibition was assessed as percent cell proliferation inhibition wherein vehicle-treated cells were taken as 0% inhibition.
Protein preparation and western blot analysis
HCC cells (50% confluent) were treated with 10, 20, 30 μmol/L of lupeol, 1 μmol/L, 3 μmol/L of S14161 alone or in combination with 20 μmol/L lupeol for 48 h in 10% fetal bovine serum-DMEM. Cells were then harvested and cell lysates were prepared using Cytoplasmic Protein Extraction Kit (Beyotime, Nantong, China) and stored at -80°C for later use. The protein content in the lysates was measured by BCA Protein Assay Kit (Beyotime, Nantong, China). For Western blot analysis, 25 μg of protein were resolved over 12% tris-glycine polyacrylamide gels under nonreduced conditions, transferred onto PVDF membranes, and subsequently incubated in blocking buffer (5% nonfat dry milk in PBS) overnight at 4°C. The blots were incubated with appropriate primary antibody, washed, and incubated with horseradish peroxidase (HRP)-conjugated secondary antibody (Dako, Carpinteria, CA). The blots were detected with chemiluminescence (ECL-Kit, Beyotime, Nantong, China) followed by autoradiography. Relative amounts of proteins were quantified by absorbance analysis. The level was normalized to β-actin, a domestic loading control.
A total of 2 × 106 SMMC7721 cells suspended in 200 μl PBS were inoculated s.c. into the right flank of 6- to 8-week-old female athymic nude mice (BALB/c-nu/nu). Treatment was started once the size of the xenograft reached approximately 4 × 4 mm. The mice were randomly assigned into four groups, each consisting of 6 mice. They were treated with intraperitoneal injection for 3 weeks of either (1) 20 mg/kg lupeol in 0.1 mL of corn oil, (2) 20 mg/kg S14161 in 0.1 mL corn oil, (3) 20 mg/kg lupeol plus 20 mg/kg S14161 in 0.1 mL corn oil, or (4) 0.1 mL of corn oil alone as the control group. Lupeol was injected three times/week (total 9 times), while S14161 was injected once/day for five continuous days/week (total 15 times). Animals in all the groups were observed for any apparent signs of toxicity, such as weight loss or mortality during the entire period of study. Tumor growth was assessed weekly by measuring the two greatest perpendicular tumor dimensions. Tumor volume was calculated by the formula: tumor volume (mm3) = [tumor length (mm) × tumor width (mm)2]/2 (34). All animals were sacrificed at the end of 5 weeks. Animal studies were carried out in accordance with the national guidelines for animal experiments and were specifically approved by the Ethical Committee of Soochow University. The body weight and the tumor size were carefully monitored and all efforts were made to minimize suffering.
All data represents at least three independent experiments and results were shown as mean ± SD. Statistical differences between two groups were determined by Student’s t-test. Analysis of variance (ANOVA) analysis was applied for multiple group comparison. A significant difference was considered as p < 0.05.
Low doses of lupeol promoted the viability and activated the PI3K/Akt pathway in HCC cell lines
Synergistic anti-HCC effect of S14161 and lupeol in vitro
We then investigated the activity of the PI3K/Akt pathway with single or combined treatment of low dose lupeol and S14161. As shown in Figure 2E, the expression levels of PI3K subunit p110 and phosphorylated Akt were increased with the 20 μmol/L lupeol treatment. Not surprisingly, the PI3K inhibitor, S14161 slightly reduced the level of phosphorylated Akt at 1 and 3 μmol/L concentrations and this reduction was maintained when S14161 was combined with lupeol treatment. The phosphorylated Akt was also significantly reduced with 3 μmol/L S14161 and the combined treatment with lupeol in HepG2 cells (Figure 2F). These results suggested that PI3K/Akt pathway activation by low doses of lupeol could be reversed by combinational treatment with PI3K inhibitor, S14161.
Synergistic anti-HCC effect of S14161 and lupeol in vivo
Previous studies have focused on the anti-tumor effects and mechanisms of lupeol in HCC. Studies have shown that lupeol induced apoptosis of SMMC7721 cells by down-regulating death receptor 3 (DR3) . Lupoel could also target liver tumor-initiating cells (T-ICs) though modulating PTEN-Akt-ABCG2 pathway . Our previous work also proved anti-HCC efficacy of lupeol and a combined effect with rTRAIL in inducing chemo-sensitization of HCC . In this report, we first described the tumor-promoting role of lupeol at low doses. We discovered that PI3K/Akt pathway was activated by low concentrations of lupeol treatment. We further demonstrated that inhibition of the PI3K/Akt pathway enhanced the antitumor effect of lupeol and the combination therapy of lupeol and S14161 synergistically promoted therapeutic effect on HCC.
PI3K/Akt pathway is critically involved in the control of cell growth, cell survival and malignant transformation . Blockage of PI3K/Akt signaling pathway results in programmed cell death and growth inhibition of tumor cells. An Akt inhibitor, perifosine, showed synergistic antitumor effect with cisplatin in HepG2 cells through down-regulating the expression of Bcl-2 and up-regulating the level of Bax . A PI3K inhibitor, LY294002, also showed synergistic antitumor effect with cisplatin in human pancreatic cancer cells by down-regulating the phosphorylated levels of Bad protein . Recently, S14161 showed potent anti-leukemia and anti-myeloma activity in vitro and inhibited in vivo tumor growth through inhibiting the activity of PI3K . Lupeol has also been reported to inhibit skin cancer in CD-1 mice through inhibition of TPA-induced activation of PI3K and phosphorylated level of Akt at Thr308 . However, this study was performed in vivo at relatively high concentrations of lupeol (1 or 2 mg/mouse). We have also observed inhibition of Akt phosphorylation at 50 μmol/L lupeol or higher in vitro (data not shown). On the other hand, low doses of lupeol could promote PI3K/Akt pathway, especially at 10-20 μmol/L concentrations, which suggested that lupeol could function through different targets that had opposite effects on PI3K/Akt pathway with different affinities.
Many natural products have been found to have multiple targets, which allow them to have multiple pharmacological activities. Lupeol has been shown to exhibit anti-inflammatory, anti-microbial, anti-protozoal, anti-tumor, anti-angiogenic and cholesterol lowering activities . The mechanism of the anti-tumor effect of lupeol was initially thought to be inhibiting NFκB . Wnt/β-catenin pathway was also found to be suppressed by lupeol in treating human melanoma cells . Lupoel could also target liver tumor-initiating cells (T-ICs) though modulating PTEN-Akt-ABCG2 pathway . Recently, lupeol has been found to be a novel androgen receptor inhibitor that may be effective in treating prostate cancer . Therefore, many signaling pathways may work together to exert the anti-tumor effect of lupeol. We propose based on our findings that lupeol may have a target with high affinity that promotes PI3K/Akt activities and tumor cell growth at low doses. At high concentrations of lupeol, the low affinity targets of lupeol dominate and regulate the signaling pathways that eventually lead to the suppression of tumor cell growth.
Taken together, our results demonstrated that lupeol could target to activate PI3-kinase/Akt pathway and promote tumor cell growth at low doses. Combination therapy of lupeol and a PI3-kinase inhibitor, S14161, could synergistically enhance the antitumor effect of lupeol in vitro and in vivo. Therefore, our results support the notion that lupeol combining with PI3-kinase inhibitor may provide more effective anti-HCC regimen.
This work has been supported in part by the grants from National Natural Science Foundation of China (91029703, 81072436 and 81273268), the project funding from Suzhou city (SS201032, SZS201109), Priority Academic Program Development of Jiangsu Higher Education Institutions, Qing Lan project of Jiangsu Province, Jiangsu Provincial Innovative Research Team, and Program for Changjiang Scholars and Innovative Research Team in University (IRT1075). We would like to thank Dr. Dapeng Zhou, MD Anderson Cancer Center, for critical reading of the manuscript.
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