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. 2014 Aug 7;111(7):1327–1337. doi: 10.1038/bjc.2014.422

Negative regulation of signal transducer and activator of transcription-3 signalling cascade by lupeol inhibits growth and induces apoptosis in hepatocellular carcinoma cells

K S Siveen 1,8, A H Nguyen 1,8, J H Lee 2,8, F Li 1, S S Singh 1,3, A P Kumar 1,3,4,5, G Low 3,6, S Jha 3,6, V Tergaonkar 7, K S Ahn 2,*, G Sethi 1,3,*
PMCID: PMC4183851  PMID: 25101566

Abstract

Background:

Constitutive activation of signal transducer and activator of transcription signalling 3 (STAT3) has been linked with survival, proliferation and angiogenesis in a wide variety of malignancies including hepatocellular carcinoma (HCC).

Methods:

We evaluated the effect of lupeol on STAT3 signalling cascade and its regulated functional responses in HCC cells.

Results:

Lupeol suppressed constitutive activation of STAT3 phosphorylation at tyrosine 705 residue effectively in a dose- and time-dependent manner. The phosphorylation of Janus-activated kinases (JAKs) 1 and 2 and Src was also suppressed by lupeol. Pervanadate treatment reversed the downregulation of phospho-STAT3 induced by lupeol, thereby indicating the involvement of a phosphatase. Indeed, we observed that treatment with lupeol increased the protein and mRNA levels of SHP-2, and silencing of SHP-2 abolished the inhibitory effects of lupeol on STAT3 activation. Treatment with lupeol also downregulated the expression of diverse STAT3-regulated genes and decreased the binding of STAT3 to VEGF promoter. Moreover, the proliferation of various HCC cells was significantly suppressed by lupeol, being associated with substantial induction of apoptosis. Depletion of SHP-2 reversed the observed antiproliferative and pro-apoptotic effects of lupeol.

Conclusions:

Lupeol exhibited its potential anticancer effects in HCC through the downregulation of STAT3-induced pro-survival signalling cascade.

Keywords: hepatocellular carcinoma, STAT3, SHP-2, lupeol, apoptosis

Hepatocellular carcinoma (HCC) is the most common tumour that originates in the liver, accounting for 70% to 85% of the total liver cancer burden worldwide. It has great heterogeneity with respect to tumour behaviour and disease of the underlying liver, and primarily develops from chronic infections caused by hepatitis B and hepatitis C viruses, alcoholic injury and to a lesser extent from genetically determined disorders such as haemochromatosis (Jemal et al, 2011; Baffy et al, 2012). Untreated HCC has an extremely poor prognosis, with a median survival of 1–8 months and a 5-year survival of ∼3% (Cormier et al, 2006). Existing treatment options including surgical resection and use of chemotherapy and/or radiotherapy are commonly associated with severe side effects, and are also limited by therapeutic resistance and disease recurrence (Cervello et al, 2012; Subramaniam et al, 2013). Hence, identification of novel agents that are nontoxic and efficacious is urgently required for both prevention and treatment of HCC.

The signal transducer and activator of transcription signalling 3 (STAT3) protein belongs to the STAT family of transcription factors that are activated in response to cytokines and growth factors (Ihle, 1996). Ligand-dependent activation of STAT regulatory cascades is involved in the regulation of a variety of critical functions, including cell differentiation, proliferation, apoptosis, angiogenesis, metastasis and immune responses (Wang et al, 2011). The abnormal activation of STAT proteins is frequently associated with unrestricted cell growth and malignant transformation (Grivennikov and Karin, 2010). Most of the major human malignancies as well as tumour-derived cell lines have been reported to contain constitutively activated STAT proteins, especially STAT3 (Johnston and Grandis, 2011). The STAT3 has been classified as an oncogene because the constitutively active STAT3 can mediate oncogenic transformation in cultured cells and tumour formation in nude mice (Burke et al, 2001). The STAT3 and NF-κB are two major transcription factors regulating the ability of pre-neoplastic and malignant cells to resist tumour surveillance, and the inflammatory milieu promoted by these proteins is one of the key properties that tumours must acquire for transformation (Dey et al, 2008; Ghosh et al, 2012). Activation of STAT3 provides a growth advantage to tumour cells, allowing accumulation, and also confers resistance to conventional therapies that rely on apoptotic machinery to eliminate tumour cells (Rajendran et al, 2012; Subramaniam et al, 2013). Thus, pharmacological modulation of STAT3 protein can be considered as an attractive strategy for cancer prevention and treatment.

One major source of pharmacological inhibitors of STAT3 are agents derived from natural sources, as ∼70% of all anticancer drugs being used in clinical therapy are isolated from natural sources or bear a close structural relationship to compounds of natural origin (Newman, 2008). In the present study, we have investigated for the first time the effect of lupeol (Lup-20(29)-en-3H-ol), a naturally occurring dietary pentacyclic triterpene found in a variety of fruits, vegetables and medicinal plants, on STAT3 signalling cascade in HCC cells. The quantification studies have shown that lupeol is present in a significant quantity in olives (3 μg g−1), mangoes (1.80 μg per pulp), aloe leaf (280 μg per dry leaf), elm plant (800 μg per bark), Japanese pear (175 μg  per g twig bark) and ginseng oil (15.2 mg per 100 g of oil) (Siddique et al, 2011). Lupeol has exhibited strong antioxidant, anti-inflammatory, antiarthritic, antimutagenic and antimalarial activities in several previously reported in vitro and in vivo studies (Siddique and Saleem, 2011). Lupeol has been shown to exert substantial antitumour effects in multiple tumour cell lines and cancer models (Siddique and Saleem, 2011) and has been found to target Wnt/β-catenin signalling in human melanoma cells (Tarapore et al, 2010), sensitise castration-resistant prostate cancer cells to antihormone therapy (Siddique et al, 2011), induce apoptosis in head and neck squamous cell carcinoma by suppressing NF-κB activation (Lee et al, 2007), inhibit the self-renewal ability of liver tumour-initiating cells (T-ICs) present in both HCC cell lines and clinical samples (Lee et al, 2011b) and induce apoptosis in human epidermoid carcinoma cells through negative regulation of mitochondrial, Akt/PKB and NF-κB signalling pathways (Prasad et al, 2009).

In the present report, we investigated whether lupeol can mediate its anticancer effects in part through the modulation of the STAT3 activation pathway. We observed that lupeol can indeed negatively regulate both constitutive and inducible STAT3 activation, leading to suppression of proliferation, induction of apoptosis and downregulation of expression of various proliferative, anti-apoptotic and angiogenic gene products in HCC cells.

Materials and methods

Reagents

Lupeol was obtained from Sigma-Aldrich (St Louis, MO, USA). It was resuspended in warm alcohol and diluted in dimethyl sulphoxide (DMSO) to make 10 mM stock solution and stored at 4 °C. Further dilution was done in cell culture medium as required. MTT, Tris, glycine, NaCl, SDS and BSA were purchased from Sigma-Aldrich. Fetal bovine serum (FBS), RPMI-1640, 0.4% Trypan blue vital stain, Lipofectamine 2000 and antibiotic–antimycotic mixture were obtained from Invitrogen (Carlsbad, CA, USA). Mouse monoclonal antibodies to Bcl-xL, Bcl-2, survivin, VEGF and caspase-9 and rabbit polyclonal antibodies to cyclin D1, MMP-9, SHP-2 (SH-PTP2), Bak, Bax, Bid, caspase-3, PARP and IL-6Rα were obtained from Santa Cruz Biotechnology (San Diego, CA, USA). Mouse monoclonal antibodies to STAT3 and caspase-8 and rabbit monoclonal antibodies against phospho- STAT3 (Tyr 705), phospho-specific Src (Tyr 416), Src, phospho-specific Janus-activated kinase 1 (JAK1; Tyr 1022/1023), JAK1, phospho-specific JAK2 (Tyr 1007/1008), JAK2 and Bid (polyclonal) were purchased from Cell Signaling Technology (Beverly, MA, USA). The siRNA for SHP-2 and scrambled control was obtained from Santa Cruz Biotechnology. Goat anti-rabbit-horse radish peroxidase (HRP) conjugate and goat anti-mouse HRP were purchased from Sigma-Aldrich. LIVE/DEAD viability/cytotoxicity kit was purchased from Molecular Probes, Invitrogen (Carlsbad, CA, USA).

Cell lines

Human hepatocellular carcinoma (HCC) cell lines HepG2 and C3A were obtained from American Type Culture Collection (Manassas, VA, USA). The PLC/PRF5, HUH-7 and Hep3B cells were kindly provided by Professor Kam Man Hui, National Cancer Centre, Singapore. All the HCC cells were cultured in Dulbecco's modified Eagle's medium (DMEM) containing 1 × antibiotic–antimycotic solution with 10% FBS.

EMSA for STAT3 DNA binding

The STAT3 DNA binding was analysed by electrophoretic mobility shift assay (EMSA) using a 32P-labelled high-affinity sis-inducible element (hSIE) probe (5′-CTTCATTTCCCGTAAATCCCTA-AAGCT-3′ and 5′-AGCTTTAGGGATTTACGGGAAATGA-3′) as previously described (Bhutani et al, 2007). Briefly, nuclear extracts were prepared from lupeol-treated cells and incubated with the labelled hSIE probe. The DNA–protein complex formed was separated from free oligonucleotide on 5% native polyacrylamide gels. To confirm the specificity, competition using 30-fold excess unlabelled oligonucleotides containing consensus or mutated STAT3 binding sites were added for 20 min at room temperature, after incubation with the radio-labelled oligonucleotides. The dried gels were visualised, and the radioactive bands were quantitated with a Universal Hood II (Bio-Rad Laboratories, Hercules, CA, USA). For additional information, please refer to Supplementary Materials and Methods.

Statistical analysis

Data are expressed as the mean±s.d. In all figures, vertical error bars denote the s.d. The significance of differences between groups was evaluated by Student's t-test and one-way analysis of variance (ANOVA) test. A P-value of <0.05 was considered statistically significant.

Results

Lupeol inhibits constitutive STAT3 phosphorylation in HepG2 cells

The HepG2 cells have been shown to express constitutive STAT3 activation (Rajendran et al, 2011; Lepiller et al, 2013), and hence we set out to determine whether lupeol could inhibit this activation in these cells. The HepG2 cells were incubated with different concentrations of lupeol for 6 h, and the phosphorylation of STAT3 was examined by western blot analysis using antibodies that recognise STAT3 phosphorylation at tyrosine 705. As shown in Figure 1B, lupeol inhibited the constitutive activation of STAT3 in a dose-dependent manner, with maximum inhibition occurring at ∼50 μM. Lupeol had no effect on the expression of STAT3 protein (Figure 1B, lower panel). We also determined the length of incubation time required for the suppression of STAT3 activation by lupeol. As shown in Figure 1C, the inhibition was time dependent, with complete inhibition occurring at ∼6 h, again with no effect on the expression of STAT3 protein (Figure 1C, lower panel).

Figure 1.

Figure 1

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(A) The chemical structure of lupeol. (B) Lupeol suppresses phospho-STAT3 levels in a dose-dependent manner. HepG2 cells (2 × 106 per ml) were treated with the indicated concentrations of lupeol for 6 h, after which whole-cell extracts were prepared and 30 μg of protein was resolved on 10% SDS–PAGE gel, electrotransferred onto nitrocellulose membranes and probed for phospho-STAT3. The same blots were stripped and reprobed with STAT3 antibody to verify equal protein loading. (C) Lupeol suppresses phospho-STAT3 levels in a time-dependent manner. The HepG2 cells (2 × 106 per ml) were treated with the 50 μM lupeol for the indicated times, after which western blotting was performed as described in (B). The same blots were stripped and reprobed with STAT3 antibody to verify equal protein loading. (D) Lupeol suppresses STAT3 DNA-binding ability in a dose-dependent manner in HepG2 cells. The HepG2 cells were treated with the indicated concentrations of lupeol for 6 h; nuclear extracts were prepared and analysed by EMSA using the radiolabelled oligonucleotide containing hSIE as described in the Materials and Methods. (E) Lupeol suppresses STAT3 DNA-binding ability in HepG2 cells. The HepG2 cells were treated with 50 μM lupeol for indicated time points; nuclear extracts were prepared and analysed by EMSA using the radiolabelled oligonucleotide containing hSIE as described in the Materials and Methods. (F) The EMSA competition assay demonstrating specificity of STAT3 binding. Nuclear extracts of untreated HepG2 cells were prepared and analysed by EMSA using radiolabelled oligonucleotide containing hSIE along with 30-fold excess competitor (an unlabelled oligonucleotide probe) and mutator (an unlabelled probe with a mutation that abrogates STAT3 DNA binding). (G) Lupeol causes inhibition of translocation of STAT3 to the nucleus. The HepG2 cells (1 × 105 per ml) were incubated with or without 50 μM lupeol for 6 h and then analysed for the intracellular distribution of STAT3 by immunocytochemistry. The same slides were counterstained for nuclei with 1 μg ml−1 DAPI for 5 min. The results shown are representative of two independent experiments.

Lupeol inhibits STAT3 DNA-binding activity in HepG2 cells

The phosphorylation of STAT3 promotes homodimerisation, and the STAT3 dimers translocate to the nucleus, where they bind to specific DNA response elements in the promoter regions of responsive target genes to regulate their transcription (Johnston and Grandis, 2011; Subramaniam et al, 2013). Hence, we determined whether lupeol can suppress DNA-binding activity of STAT3. The EMSA analysis of nuclear extracts prepared from HepG2 cells showed that lupeol caused a decrease in STAT3 DNA-binding activity in a dose- (Figure 1D) and time-dependent manner (Figure 1E). Addition of excess unlabeled oligonucleotide (competitor; 30-fold molar excess) caused a complete disappearance of the band, whereas mutated oligonucleotide had no effect on DNA binding (Figure 1F).

Lupeol reduces nuclear pool of STAT3 in HCC cells

As nuclear translocation is central towards the functional activity of transcription factors such as STAT3 (Subramaniam et al, 2013), we determined whether lupeol can suppress nuclear translocation of STAT3. Figure 1F clearly demonstrates that lupeol inhibited the translocation of STAT3 to the nucleus in HepG2 cells.

Lupeol suppresses constitutive activation of c-Src

Signal transducer and activator of transcription signalling 3 has also been reported to be activated by soluble tyrosine kinases of the Src kinase families (Yu et al, 1995; Subramaniam et al, 2013). Hence, we determined the effect of lupeol on constitutive activation of Src kinase in HepG2 cells. We found that lupeol suppressed the constitutive phosphorylation of c-Src kinases (Figure 2A). The levels of nonphosphorylated Src kinases remained unchanged under the same conditions.

Figure 2.

Figure 2

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Lupeol inhibits constitutively active STAT3 in HCC cells. (A) Lupeol suppresses phospho-Src levels in a time-dependent manner. The HepG2 cells (2 × 106 per ml) were treated with 50 μM lupeol, after which whole-cell extracts were prepared and 30 μg aliquots of those extracts were resolved on 10% SDS–PAGE, electrotransferred onto nitrocellulose membranes and probed for phospho-src antibody. The same blots were stripped and reprobed with Src antibody to verify equal protein loading. (B) Lupeol suppresses phospho-JAK1 levels in a time-dependent manner. HepG2 cells (2 × 106 per ml) were treated with 50 μM lupeol for indicated time intervals, after which whole-cell extracts were prepared and 30 μg portions of those extracts were resolved on 10% SDS–PAGE, electrotransferred onto nitrocellulose membranes and probed against phospho-JAK1 antibody. The same blots were stripped and reprobed with JAK1 antibody to verify equal protein loading. (C) Lupeol suppresses phospho-JAK2 levels in a time-dependent manner. The HepG2 cells (2 × 106 per ml) were treated with 50 μM lupeol for indicated time intervals, after which whole-cell extracts were prepared and 30 μg portions of those extracts were resolved on 10% SDS–PAGE, electrotransferred onto nitrocellulose membranes and probed against phospho-JAK2 antibody. The same blots were stripped and reprobed with JAK2 antibody to verify equal protein loading. (D) Pervanadate reverses the phospho-STAT3 inhibitory effect of lupeol. The HepG2 cells (2 × 106 per ml) were treated with the indicated concentrations of pervanadate and 50 μM lupeol for 6 h, after which whole-cell extracts were prepared and 30 μg portions of those extracts were resolved on 10% SDS–PAGE gel, electrotransferred onto nitrocellulose membranes and probed for phospho-STAT3 and STAT3. (E) Lupeol induces the expression of SHP-2 protein in HepG2 cells. The HepG2 cells were treated with indicated concentrations of lupeol for 6 h, after which western blotting was performed using SHP-2, SHP-1 and β-actin antibodies. (F) Lupeol induces the expression of SHP-2 in HepG2 cells. The HepG2 cells were treated with indicated concentrations of lupeol for 6 h, after which total RNA was extracted, and the mRNA level of SHP-2 was analysed by RT–PCR. Glyceraldehyde 3-phosphate dehydrogenase (GAPDH) was used as an internal control. (G) Effect of SHP-2 knockdown on lupeol-induced expression of SHP-2. The HepG2 cells were transfected with either SHP-2 siRNA or scrambled siRNA (50 nM). After 24 h, cells were treated with 50 μM lupeol for 6 h and whole-cell extracts were subjected to western blot analysis. (H) The HepG2 cells were transfected with either SHP-2 siRNA or scrambled siRNA (50 nM). After 24 h, cells were treated with 50 μM lupeol for 6 h and whole-cell extracts were subjected to western blot analysis for phosphorylated STAT3. The results shown are representative of two independent experiments.

Lupeol suppresses constitutive activation of JAK1 and JAK2

Because JAKs phosphorylate STAT proteins when activated by signals from interleukins and other cytokines (Subramaniam et al, 2013), we next analysed whether lupeol can affect constitutive activation of JAK1 in HepG2 cells. We found that lupeol suppressed the constitutive phosphorylation of JAK1 (Figure 2B), with maximum inhibition at 6 h. The levels of nonphosphorylated JAK1 remained unchanged under the same conditions (Figure 2B, bottom panel). To determine the effect of lupeol on JAK2 activation, HepG2 cells were treated for different time intervals with lupeol and phosphorylation of JAK2 was analysed by western blot. As shown in Figure 2C, JAK2 was constitutively active in HepG2 cells and pretreatment with lupeol suppressed this phosphorylation in a time-dependent manner.

Tyrosine phosphatases are involved in lupeol-induced inhibition of STAT3 activation

Several protein tyrosine phosphatases (PTPs) have been implicated in the termination of STAT3 signalling, including SHP-2, PTP1B, PTPɛC, TC45 and SHP-1 (Johnston and Grandis, 2011; Subramaniam et al, 2013). To investigate whether lupeol-induced inhibition of STAT3 tyrosine phosphorylation involves activation of any protein tyrosine phosphatase (PTPase), we treated HepG2 cells with the broad-acting tyrosine phosphatase inhibitor sodium pervanadate and looked for reversal of lupeol-induced suppression of STAT3 activation (Figure 2D). These data suggest that tyrosine phosphatases may be involved in lupeol-induced inhibition of STAT3 activation in HCC cells.

Lupeol induces the expression of SHP-2 in HCC cells

The SHP-2 is a SH-2 containing tyrosine phosphatase involved in the suppression of a variety of cytokine signals, including STAT3 (Wormald and Hilton, 2004). Hence, we next examined whether lupeol can induce the expression of SHP-2 and SHP-1 in HepG2 cells. The cells were incubated with 50 μM lupeol for different time points ranging from 1 to 6 h, and whole-cell extracts were prepared and examined for SHP-2 and SHP-1 protein expression by western blot analysis. As shown in Figure 2E, lupeol significantly induced the expression of SHP-2 protein in HepG2 cells in a time-dependent manner, with maximum expression at 4–6 h, whereas it had minimal effect on the expression of SHP-1 protein. The increase in SHP-2 expression by lupeol correlated with downregulation of constitutive STAT3 activation in HepG2 cells (Figure 1C). The two sets of data point to the fact that stimulation of SHP-2 expression by lupeol mediates the downregulation of constitutive STAT3 activation in HepG2 cells. Whether modulation of SHP-2 by lupeol is also regulated at the transcriptional level was investigated as well. For this, cells were incubated with different concentrations of lupeol for 6 h, and then total RNA was extracted, converted to cDNA and examined for SHP-2 gene expression by reverse transcription–PCR (RT–PCR) analysis. As shown in Figure 2F, lupeol induced the expression of SHP-2 mRNA, with maximum expression at 4 to 6 h of treatment.

SHP-2 siRNA downregulate the expression of SHP-2 induced by lupeol

We determined the effect of SHP-2 siRNA on lupeol-induced SHP-2 expression. As observed by western blot analysis, lupeol-induced SHP-2 expression was effectively inhibited in the cells transfected with SHP-2 siRNA while in the cells treated with the (Figure 2G), sequence-randomised scrambled siRNA oligonucleotide no substantial effect was noticed.

SHP-2 siRNA reversed the inhibition of STAT3 activation by lupeol

We next determined whether the suppression of SHP-2 expression by siRNA abrogates the inhibitory effect of lupeol on STAT3 activation. Western blot analysis shows that lupeol failed to suppress STAT3 activation in the cells transfected with SHP-2 siRNA (Figure 2H). However, lupeol caused downregulation of STAT3 activation in cells transfected with scrambled siRNA. These results suggest the pivotal role of SHP-2 in suppression of STAT3 phosphorylation by lupeol.

Lupeol inhibits inducible STAT3, JAK1 and JAK2 phosphorylation in HCC cells

Because IL-6 induces STAT3 phosphorylation, we next determined whether lupeol could inhibit IL-6-induced STAT3 phosphorylation in HCC cells. In Hep3B cells incubated with lupeol for different times, IL-6-induced STAT3, JAK1 and JAK2 phosphorylation was suppressed by lupeol in a time-dependent manner. Exposure of cells to lupeol for 4 h was sufficient to substantially suppress IL-6-induced STAT3 phosphorylation in Hep3B cells (Figure 3A). These results suggest that lupeol can also downregulate inducible STAT3 activation in HCC cells. Moreover, IL-6-induced STAT3 phosphorylation was blocked by neutralising IL-6 receptor antibodies, thereby indicating the specificity of STAT3 phosphorylation induced by IL-6 in Hep3B cells (Figure 3A, last lane).

Figure 3.

Figure 3

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Lupeol downregulates IL-6-induced phospho-STAT3 in HCC cells. (A) The Hep3B cells (2 × 106 per ml) were treated with 50 μM lupeol for the indicated times and then stimulated with IL-6 (10 ng ml−1) for 15 min. One set of Hep3B cells were preincubated for 18 h in the presence of neutralising IL-6 receptor antibody (1 μg ml−1) before stimulation with IL-6 to serve as a positive control. Whole-cell extracts were then prepared and analysed for p-STAT3 by western blotting. The same blots were stripped and reprobed with STAT3 antibody to verify equal protein loading. (B) The Hep3B cells (2 × 106 per ml) were treated with 50 μM lupeol for the indicated times and then stimulated with IL-6 (10 ng ml−1) for 15 min. One set of Hep3B cells were preincubated for 18 h in the presence of neutralising IL-6 receptor antibody (1 μg ml−1) before stimulation with IL-6 to serve as a positive control. Whole-cell extracts were then prepared and analysed for p-JAK1 by western blotting. The same blots were stripped and reprobed with JAK1 antibody to verify equal protein loading. (C) The Hep3B cells (2 × 106 per ml) were treated with 50 μM lupeol for the indicated times and then stimulated with IL-6 (10 ng ml−1) for 15 min. One set of Hep3B cells were preincubated for 18 h in the presence of neutralising IL-6 receptor antibody (1 μg ml−1) before stimulation with IL-6 to serve as a positive control. Whole-cell extracts were then prepared and analysed for p-JAK2 by western blotting. The same blots were stripped and reprobed with JAK2 antibody to verify equal protein loading. (D) The PLC/PRF5 cells (5 × 105 per ml) were transfected with STAT3-luciferase (STAT3-Luc) plasmid, incubated for 48 h and treated with indicated doses of lupeol for 6 h and then stimulated with EGF (100 ng ml−1) for 2 h. Whole-cell extracts were then prepared and analysed for luciferase activity. The results shown are representative of two independent experiments. *P<0.05. Abbreviation: DN=dominant negative.

Lupeol suppresses EGF-induced STAT3-dependent reporter gene expression in HCC cells

Our above results showed that lupeol inhibited the phosphorylation and nuclear translocation of STAT3. We next determined whether lupeol affects STAT3-dependent gene transcription. When PLC/PRF5 cells transiently transfected with the pSTAT3-Luc construct were stimulated with EGF, STAT3-mediated luciferase gene expression was increased. Transfection with dominant-negative STAT3 blocked this increase, indicating specificity. When the cells were pretreated with lupeol, EGF-induced STAT3 activity was inhibited in a dose-dependent manner (Figure 3D).

Lupeol downregulates the expression of various antiproliferative, anti-apoptotic and angiogenic gene products in HCC cells

The persistently activated STAT3 proteins in tumour cells promote a permanent alteration of various oncogenic genes that control cellular processes such as proliferation, survival, invasion, angiogenesis and chemoresistance (Wang et al, 2011). Treatment of HepG2 cells with lupeol was found to downregulate the expression of the cell cycle regulator (cyclin D1), the antiapoptotic proteins (Bcl-xL, survivin), the angiogenic gene product VEGF and an important matrix metalloproteinase-9 (MMP-9) that is involved in the degradation of cellular matrix, all of which have been reported to be regulated by STAT3. Their expression decreased in a time-dependent manner, with maximum suppression observed at ∼48 h (Figure 4A). We also found that mRNA expression of survivin and Mcl-1 was modulated by lupeol treatment in a time-dependent manner, with maximum reduction observed at ∼24 h after treatment (Figure 4B).

Figure 4.

Figure 4

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Lupeol suppresses expression of STAT3-regulated gene products involved in proliferation, survival and angiogenesis. (A) The HepG2 cells (2 × 106 per ml) were treated with 50 μM lupeol for indicated time intervals, after which whole-cell extracts were prepared and 30 μg portions of those extracts were resolved on 10% SDS–PAGE, membrane sliced according to molecular weight and probed against cyclin D1, Bcl-xL, survivin, VEGF and MMP-9 antibodies. The same blots were stripped and reprobed with β-actin antibody to verify equal protein loading. The results shown are representative of two independent experiments. (B) The HepG2 cells (3 × 105 per ml) were treated with 50 μM lupeol for the indicated time intervals, after which cells were harvested after treatment and RNA samples were extracted. Then, 1 μg portions of the respective RNA extracts was used for reverse transcription to generate corresponding cDNA. Real-time PCR was performed to measure the relative quantities of mRNA. Each RT product was targeted against Mcl-1 and survivin probes, with GAPDH as endogenous control for measurement of equal loading of RNA samples. Results were analysed using Sequence Detection Software version 1.3 provided by Applied Biosystems. Relative gene expression was obtained after normalisation with endogenous GAPDH and determination of the difference in threshold cycle (Ct) between treated and untreated cells using 2-ΔΔCt method. (C) Treatment with lupeol decreases binding of STAT3 to VEGF promoter. Chromatin immunoprecipitation (ChIP) assay was performed in HepG2 cells to examine binding of STAT3 on VEGF promoter. Cells were treated with lupeol for indicated time and crosslinked. The cell pellets were processed for ChIP as detailed under Supplementary Materials and Methods. Ratio of quantitative real-time PCR signal in STAT3 immunoprecipitate relative to IgG (negative control) immunoprecipitate is plotted. Mean±s.d. of three experiments (*P<0.05).

Exposure of HCC cells to lupeol decreases binding of STAT3 to VEGF promoter

In order to understand the mechanism of decrease in STAT3-regulated gene expression, we next performed ChIP experiments. For this, lupeol- or vehicle-treated cells were crosslinked at indicated time post lupeol treatment, and in vivo binding of STAT3 was investigated. Treatment with lupeol resulted in a significant decrease in STAT3 binding to VEGF promoter in a time-dependent manner (Figure 4C). These data suggest that upon exposure to lupeol, a decrease in expression of STAT3 target genes is observed because of a decreased STAT3 binding to its promoter.

Lupeol inhibits the proliferation of HCC cells in a dose- and time-dependent manner

As treatment with lupeol was found to downregulate the expression of cyclin D1, a gene involved in cell proliferation, we investigated whether lupeol can inhibit the proliferation of various HCC cells using the MTT assay. Lupeol inhibited proliferation of C3A, HepG2, PLC/PRF5 and HUH-7 cells in a dose- and time-dependent manner (Figure 5A).

Figure 5.

Figure 5

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(A) The HepG2, PLC/PRF5, HUH-7 and C3A cells (5 × 103 per ml) were plated in triplicate, treated with indicated concentrations of lupeol and then subjected to MTT assay after 24, 48 and 72 h to analyse proliferation of cells. The s.d. values between triplicates are indicated. (B) The HepG2 cells (2 × 106 per ml) were treated with 50 μM lupeol for the indicated times, after which the cells were washed, fixed, stained with PI and analysed for DNA content by flow cytometry. (C) The HepG2 cells were treated with 50 μM lupeol for the indicated times, whole-cell extracts were prepared, separated on SDS–PAGE and subjected to western blotting against Bak, Bax and Bcl-2 antibodies. (D) The HepG2 cells were treated with 50 μM lupeol for the indicated times, whole-cell extracts were prepared, separated on SDS–PAGE and subjected to western blotting against Bid and cleaved Bid antibodies. The same blots were stripped and reprobed with β-actin antibody to show equal protein loading. (E) The HepG2 cells were treated with 50 μM lupeol for the indicated times, whole-cell extracts were prepared, separated on SDS–PAGE and subjected to western blotting against pro-caspase-8, pro-caspase-9, pro-caspase-3 and cleaved caspase-3 antibodies. The same blot was stripped and reprobed with β-actin antibody to show equal protein loading. (F) The HepG2 cells were treated with 50 μM lupeol for the indicated times, and whole-cell extracts were prepared, separated on SDS–PAGE and subjected to western blot against PARP antibody. The same blot was stripped and reprobed with β-actin antibody to show equal protein loading. The results shown are representative of two independent experiments.

Lupeol causes the accumulation of the cells in the sub-G1 phase of the cell cycle

To further confirm that lupeol inhibits proliferation of HCC cells through induction of apoptosis, we analysed cell cycle distribution after PI staining. We found that lupeol increased the accumulation of the cell population in the sub-G1 phase after treatment for 6, 12 and 24 h in a time-dependent manner, indicative of cellular apoptosis (Figure 5B).

Lupeol upregulates the expression of Bak and Bax and downregulates Bcl-2

We found that lupeol-treated HepG2 cells had an increase in the expression of the pro-apoptotic proteins Bak and Bax, with maximum upregulation observed at 48 h (Figure 5C). The expression of another important anti-apoptotic protein, Bcl-2, was also substantially inhibited by lupeol in a time-dependent manner (Figure 5C).

Lupeol modulates the expression of Bid

Whether lupeol can modulate the expression of pro-apoptotic protein, Bid, was also examined. We found that treatment with lupeol decreased the expression of full-length Bid in a time-dependent manner in HepG2 cells (Figure 5D). In addition, we noticed that lupeol treatment caused an increase in the level of cleaved Bid.

Lupeol activates caspases and induces PARP cleavage in HCC cells

Whether suppression of constitutively active STAT3 in HepG2 cells by lupeol leads to apoptosis was also investigated. In HepG2 cells treated with lupeol, there was a time-dependent activation of the initiator caspases 8 and 9 (Figure 5E). The levels of these pro-caspases were reduced upon treatment with lupeol, with maximum effects observed at ∼48 h. There was an increase in the levels of cleaved caspase-9 that correlated with the decrease in pro-caspase-9 upon treatment with lupeol. There was also a time-dependent activation of the effector molecule pro-caspase-3, with a concomitant increase in cleaved form of caspase-3 in a time-dependent manner (Figure 5E). Activation of downstream caspases led to the cleavage of a 118-kDa poly(ADP-ribose) polymerase (PARP) protein into an 85-kDa fragment (Figure 5F). This result clearly suggests that lupeol induces caspase-3-dependent apoptosis in HepG2 cells.

Transfection with SHP-2 siRNA abrogates antiproliferative/pro-apoptotic effects of lupeol in HCC cells

The effect of silencing of the SHP-2 gene on the antiproliferative effects of lupeol was investigated using HepG2 cells transfected with SHP-2 or scrambled siRNA before treatment with lupeol. We found that lupeol decreased the proliferation of cells and that transfection with SHP-2 siRNA reversed the antiproliferative effects of lupeol (Figure 6A). These results suggest that SHP-2 plays a major role in inhibiting tumour cell proliferation through inhibition of STAT3 activation. As we found that lupeol-induced suppression in STAT3 activation was mediated through the induction of SHP-2, we investigated whether silencing of SHP-2 with siRNA can abrogate lupeol-induced apoptosis in HepG2 cells. Apoptosis was analysed through the examination of intracellular esterase activity by live/dead assay. Transfection with SHP-2 siRNA abolished lupeol-induced apoptosis (Figure 6B), and the percentage of apoptotic cells was reduced from 32.7% to 11.4%, whereas transfection with control siRNA had no significant effect on apoptosis (a decrease from 32.7% to 30.4%).

Figure 6.

Figure 6

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(A) Gene silencing of SHP-2 abolishes lupeol-induced suppression in tumour cell proliferation. The HepG2 cells were transfected with SHP-2 siRNA or control siRNA for 48 h and then treated with 50 μM lupeol for 24, 48 and 72 h. Mitochondrial dehydrogenase activity was measured at 24, 48 and 72 h after lupeol treatment. Cell proliferation was analysed by measuring absorbance at 570 nm. *P<0.05. (B) Silencing of SHP-2 suppresses lupeol-induced apoptosis. The HepG2 cells were transfected with SHP-2 siRNA or control siRNA for 48 h and treated with 50 μM for 24 h. Apoptosis was measured by live/dead assay. Values represent the mean number of apoptotic cells±s.d. Magnification × 100. (C) Wound-healing assay for evaluating effect of lupeol on the migration of HepG2 cells. An IBIDI culture insert (IBIDI GmbH) consists of two reservoirs separated by a 500 μm thick wall created by a culture insert in a 35 mm Petri dish. For migration assay, an equal number of HepG2 cell (70 μl; 5 × 105 cells per ml) were added into the two reservoirs of the same insert and incubated at 37 °C/5% CO2. After 12 h, the insert was gently removed creating a gap of ∼500 μm. The cells were treated with 50 μM lupeol for 12 h before being exposed to 100 ng ml−1 CXCL12 for 24 h. Width of wound was measured at time 0 and 24 h of incubation with and without lupeol in the absence or presence of CXCL12. The representative photographs showed the same area at time 0 and after 24 h of incubation. (D) Lupeol suppresses invasion of HepG2 cells. The HepG2 cells (2 × 105 cells) were seeded in the top chamber of the Matrigel. After preincubation with or without 50 μM lupeol for 12 h, transwell chambers were then placed into the wells of a 24-well plate, in which we had added either the basal medium only or basal medium containing 100 ng ml−1 CXCL12 in a predetermined arrangement. After incubation for 24 h, cell invasion was analysed and columns represent mean number of invaded cells. *P<0.05.

Lupeol suppresses CXCL12-induced HepG2 cell migration and invasion

Constitutively expressed STAT3 is involved in the expression of MMP-2 and MMP-9 that play a major role in tumour metastasis (Dechow et al, 2004; Li et al, 2006). Hence, whether suppression of constitutively active STAT3 in HepG2 cells by lupeol leads to inhibition in cell migration and invasion was also investigated. Effect of lupeol on HepG2 cell migration was analysed using an in vitro wound-healing assay. We found that HepG2 cells migrated faster under the influence of CXCL12 and this effect was significantly abolished on treatment with lupeol (Figure 6C). Using an in vitro invasion assay, we also found that CXCL12 significantly induced the invasion of HepG2 cells and that lupeol significantly abrogated the invasive activity (Figure 6D).

Discussion

The pivotal aim of this study was to determine whether lupeol exerts its anticancer effects through the abrogation of the STAT3 signalling pathway in HCC cells. We found that this triterpene suppressed both constitutive and inducible STAT3 activation in human HCC cells in parallel with the inhibition of JAK1, JAK2 and Src activation. Lupeol also downregulated the expression of STAT3-regulated gene products, including cyclin D1, Bcl-2, Bcl-xL, survivin, VEGF and MMP-9 proteins. It also caused the inhibition of proliferation, increased accumulation of cells in sub-G1 phase and significantly attenuated migratory and invasive potential of HCC cells. Aberrant STAT3 activation has been linked to oncogenesis in a variety of human tumours including HCC, and our studies indicate for the first time that lupeol may also exert its anticancer effects through the modulation of STAT3 signalling cascade.

Whether investigated by western blot analysis for STAT3 phosphorylation at tyrosine 705 residue, by nuclear translocation or by EMSA experiments, we noticed that lupeol substantially suppressed STAT3 activation in HCC cells. We found that lupeol also suppressed STAT3 activation induced by IL-6, one of the many tumour cell growth factors that activate STAT3 (Bromberg and Wang, 2009). The doses required to inhibit STAT3 activation were more or less comparable to rationally designed pharmacological blockers that inhibit STAT3 dimerisation (Fuke et al, 2007). The inhibitory effects of lupeol on STAT3 phosphorylation correlated with the suppression of activation of upstream protein tyrosine kinases (c-Src, JAK1 and JAK2) in a time-dependent manner in HCC cells. Prior studies have indicated that Src and JAK kinases activities cooperate to mediate constitutive activation of STAT3 in tumour cells (Garcia et al, 2001). Our data also indicate that lupeol may abrogate cooperation of Src and JAKs involved in tyrosyl phosphorylation of STAT3 in HCC cells. The roles of JAKs and Akt have been implicated in IL-6-induced STAT3 activation (Ihle, 1996; Chen et al, 1999). We found that IL-6-induced STAT3, JAK1 and JAK2 activation was also suppressed by lupeol in HCC cells. We further noticed that lupeol also suppressed nuclear translocation and EGF-induced reporter activity of STAT3. This suggests that this triterpene could manifest its effect on both constitutive and inducible STAT3 activation through multiple mechanism(s). We postulate that STAT3 inhibitory effects of lupeol as reported here can substantially contribute to its previously reported growth inhibitory and apoptotic effects in HCC cells (Baffy et al, 2012). Interestingly, it has been previously documented that lupeol can also target liver tumour-initiating cells through phosphatase and tensin homologue modulation in both HCC cell lines and clinical samples (Lee et al, 2011b). Because CD24+ liver stem cells can also drive self-renewal and tumour initiation through STAT3-mediated regulation of NANOG gene (Lee et al, 2011a), it is feasible that STAT3 inhibitory effects of lupeol may also mediate its liver stem cell-targeting effects.

The phosphorylation of STAT3 plays a key role in proliferation, survival and angiogenesis of tumour cells (Yue and Turkson, 2009). Diverse types of cancer, including head and neck (Li et al, 2013), multiple myeloma (Kannaiyan et al, 2011), prostate (Shanmugam et al, 2011), breast (Kim et al, 2013) and lymphomas and leukaemias (Zhang et al, 2002), express constitutively active STAT3. The suppression of constitutively active STAT3 in HCC cells by lupeol raises the possibility that this novel STAT3 inhibitor might also target deregulated STAT3 activation in other types of tumour cells. Moreover, it has been reported that lupeol can also abrogate several oncogenic signal transduction cascades including NF-κB, PI3K/Akt and Wnt/β-catenin in tumour cells (Siddique and Saleem, 2011). Interestingly, it has been found that STAT3 can indeed prolong NF-κB nuclear retention through acetyltransferase p300-mediated RelA acetylation, thereby interfering with NF-κB nuclear export (Lee et al, 2009). Thus, it is quite feasible that the inhibition of STAT3 activation may also mediate suppression of NF-κB signalling by lupeol.

Under normal conditions, both the amplitude and duration of receptor-induced STAT3 activation are tightly controlled by a variety of endogenous protein regulators (Cervello et al, 2012; Subramaniam et al, 2013). Numerous PTPs are involved in the regulation of JAK/STAT signalling, including SHP1, SH-PTP2, CD45, PTP1B, TC-PTP, PTPRT and PTP-BL (Xu and Qu, 2008). The SHP2 is a ubiquitously expressed SH2 domain-containing PTP. The STATs can be inactivated by SHP-2 in both the cytoplasm and the nucleus (Shuai and Liu, 2003). We found that pervanadate treatment could reverse the lupeol-induced downregulation of STAT3 in HCC cells, thereby possibly suggesting the involvement of a tyrosine phosphatase. Indeed, we noticed that lupeol treatment substantially increased the expression of SHP-2 at both protein and mRNA levels that correlated with downregulation of constitutive STAT3 phosphorylation. Transfection with SHP-2 siRNA reversed the STAT3 inhibitory effect of lupeol, thereby further implicating a critical role of this phosphatase in lupeol-induced abrogation of STAT3 activation. Interestingly, the multikinase protein tyrosine inhibitor sorafenib approved by FDA for the treatment of HCC has also found to act through a similar molecular mechanism and inhibit STAT3 activation through the induction of a phosphatase (Yang et al, 2010).

Once activated in malignant cells, STAT3 can induce the expression of a subset of genes whose products are important. Cancer cells harbouring aberrant STAT3 activity display elevated levels of anti-apoptotic (Bcl-2, Bcl-xL and survivin), cell cycle regulatory proteins (cyclin D1, c-Myc) and invasive/angiogenic gene products (MMP-9 and VEGF) (Page et al, 2011). Moreover, constitutively active STAT3 has been demonstrated to mediate uncontrolled malignant cell proliferation and directly contribute to tumourigenesis (Yue and Turkson, 2009). We analysed the effect of lupeol on proliferation and noticed that this triterpene could significantly suppress growth potential of four different HCC cell lines (HepG2, PLC/PRF5, C3A and HUH-7) in a dose- and time-dependent manner. The downregulation of cyclin D1 expression by lupeol directly correlated with suppression in proliferation as observed in various HCC cell lines. Constitutive activation of STAT3 contribute to the upregulation of Bcl-xL in ovarian cancer cell lines that contributes to the survival advantage of human ovarian carcinoma (Burke et al, 2001). Activation of STAT3 signalling can also induce expression of survivin gene that was found to confer resistance to apoptosis in human breast cancer cells (Gritsko et al, 2006). Hence, tumour cells containing persistently activated STAT3 are more resistant to environmental apoptotic cues and conventional chemotherapies that rely on the apoptotic pathway for chemotherapy-induced cell death. Thus, the downregulation of the expression of Bcl-2, Bcl-xL and survivin is likely linked with lupeol's ability to induce apoptosis that is evident by increase in accumulation of lupeol-treated cells in the sub-G1 phase, processing of the initiator caspases (caspase-8 and -9), activation of the effector caspase-3 and cleavage of PARP in HCC cells.

Our results also show that silencing SHP-2 can abrogate the inhibitory effect of lupeol on STAT3 activation, as well as abolish the antiproliferative and pro-apoptotic effects of lupeol. These findings suggest that lupeol is inhibiting tumour cell proliferation and inducing apoptosis through upregulation of SHP-2 and concomitant inhibition of STAT3 activation. The downmodulation of VEGF expression is in line with a recent report in which siRNA targeting VEGF inhibits HCC growth and tumour angiogenesis in vivo (Raskopf et al, 2008). The suppression of MMP-9 protein expression as observed here may contribute to the inhibitory effects of lupeol on the migratory and invasive potential of HCC cells. Overall, our findings indicate that lupeol interferes with several oncogenic molecules involved in tumour initiation and progression in HCC cells.

In conclusion, our data convincingly demonstrate that lupeol can negatively regulate both constitutive and inducible STAT3 activation through the suppression of upstream kinases and induction of phosphatase SHP-2 in HCC cell lines, making it a potentially effective suppressor of tumour cell survival and proliferation. Because of its potential efficacy in suppression of the deregulated STAT3 activation and low toxicity profile, lupeol may emerge as a novel candidate for HCC therapy. Additional studies in animals are required to validate these findings under in vivo settings.

Acknowledgments

This work was supported by grants from National Medical Research Council of Singapore (Grant R-184-000-211-213) to GS. KSA was supported by a grant from the Kyung Hee University in 2013 (KHU-20130546). This work was also supported by the Korea Science and Engineering Foundation (KOSEF) grant funded by the Korean Ministry of Education, Science and Technology (MoEST) (No. 2011-0006220). SJ was supported by grants from Cancer Science Institute of Singapore (R-713-006-014-271), Office of the Deputy President (Research & Technology) (R-713-000-132-133) and School of Medicine (R-713-000-132-733) at the National University of Singapore. APK was supported by grants from Singapore Ministry of Education Tier 2 (MOE 2012-T2-2-139), Academic Research Fund Tier 1 (R-184-000-228-112) and Cancer Science Institute of Singapore, Experimental Therapeutics I Program (Grant R-713-001-011-271).

Footnotes

Supplementary Information accompanies this paper on British Journal of Cancer website (http://www.nature.com/bjc)

This work is published under the standard license to publish agreement. After 12 months the work will become freely available and the license terms will switch to a Creative Commons Attribution-NonCommercial-Share Alike 3.0 Unported License.

Supplementary Material

Supplementary Information
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