Phloretin attenuates STAT-3 activity and overcomes sorafenib resistance targeting SHP-1–mediated inhibition of STAT3 and Akt/VEGFR2 pathway in hepatocellular carcinoma
Hepatocellular carcinoma (HCC) is the most common primary liver malignancy. Phloretin (PH) possesses anticancer, antitumor, and hepatoprotective effects, however, the effects and potential mechanisms of phloretin remain elusive.
Five HCC cells were tested in vitro for sensitivity to PH, Sorafenib (Sor) or both and the apoptosis, signal transduction and phosphatase activity were analyzed. To validate the role of SHP-1, we used PTP inhibitor III and SHP-1 siRNA. Further, we used purified SHP-1 proteins or HCC cells expressing deletion N-SH2 domain or D61A point mutants to study the PH efficacy on SHP-1. The `in vivo studies were conducted using HepG2 and SK-Hep1 and Sor resistant HepG2SR and Huh7SR xenografts. Molecular docking was done with Swiss dock and Auto Dock Vina.
PH inhibited cell growth and induced apoptosis in all HCC cells by upregulating SHP-1 expression and downregulating STAT3 expression and further inhibited pAKT/pERK signaling. PH activated SHP-1 by disruption of autoinhibition of SHP-1, leading to reduced p-STAT3Tyr705 level. PH induced apoptosis in two Sor-resistant cell lines and overcome STAT3, AKT, MAPK and VEGFR2 dependent Sor resistance in HCCs. PH potently inhibited tumor growth in both Sor-sensitive and Sor-resistant xenografts in vivo by impairing angiogenesis, cell proliferation and inducing apoptosis via targeting the SHP-1/STAT3 signaling pathway.
Our data suggest that PH inhibits STAT3 activity in Sor-sensitive and -resistant HCCs via SHP-1–mediated inhibition of STAT3 and AKT/mTOR/JAK2/VEGFR2 pathway. Our results clearly indicate that PH may be a potent reagent for hepatocellular carcinoma and a noveltargeted therapy for further clinical investigations.
KeywordsPhloretin Sorafenib STAT3 SHP-1 hepatocellular carcinoma
Src homology region 2 domain-containing phosphatase-1
Signal transducer and activator of transcription 3
Vascular endothelial growth factor receptor 2
Mitogen-activated protein kinase
Extracellular signal–regulated kinase;
Alpha serine/threonine-protein kinase
mechanistic target of rapamycin
protein tyrosine phosphatase
The Src homology region 2 domain-containing phosphatase-1 (SHP-1) plays a crucial role in glucose homeostasis and lipid metabolism in the liver [7, 8]. SHP-1 is one of the protein tyrosine phosphatase (PTP) members that could suppress STAT3 pathway  and dephosphorylate JAK kinases  and STAT3 directly . SHP-1 has been shown to function as a tumor suppressor to inhibit the tumor growth [12, 13]. Certain target drugs such as dovitinib and SC-2001 are known to induce apoptosis, autophagy, and HCC cell growth inhibition through enhancing the activity of SHP-1 tyrosine phosphatase in HCC [14, 15]. Various STAT3 inhibitors have been designated to directly target STAT3 mainly by inhibiting its dimerization, DNA binding, or nuclear translocation [16, 17]. However, only few of these inhibitors have demonstrated a significant blockade of STAT3 functions. Thus, identifying effective STAT3 inhibitor molecules that could revert the Sor resistance to develop individualized therapeutic strategies for clinical application in cancer is a need.
Among these promising molecules is Phloretin (PH). PH is a dihydrochalcone flavonoid (C15 H14 O5, Fig. 1b) that is mainly found in fruit, leaves, and roots of apple tree. In general, PH has high safety margin with less side effects. Several previous in vitro and in vivo studies showed that PH is not toxic to several non-cancerous cells such as epithelial breast cells MCF10A  and normal human dermal fibroblast . It has also been reported that PH scavenges ONOO- and inhibits lipid peroxidation in rat liver microsomes . Furthermore, pre- and post-treatment with PH significantly protected the liver from acetaminophen- and carbon tetrachloride (CCl4)-induced hepatotoxicity and reduced the degree of liver damage [20, 21]. Importantly, PH is shown to exhibit anticancer [22, 23], antitumor , and hepatoprotective effects with little side effects . However, the exact mechanism of the antitumor effects of PH in HCC remains uninvestigated. Therefore, the main objectives of the current work were to a) explore the molecular mechanism(s) by which PH inhibits HCC proliferation in vitro and in vivo models and b) assess the role of PH in Sor-resistant xenografts. The results of the current work clearly showed that PH exhibited anticancer potential in vitro and retarded tumor growth via targeting the SHP-1/STAT3 and AKT/VEGFR2 signaling pathway.
PH and Sor were purchased from Sigma-Aldrich (USA) and Selleck Chemicals LLC (Houston, TX). The SHP-1 inhibitor and PTP inhibitor III (CAS 29936-81-0) were purchased from Cayman Chemical (Ann Arbor, MI, USA). Smart-pool siRNA, including control (D-001810-10), SHP-1 (PTPN6) were all obtained from Dharmacon Inc. (Chicago, IL). The mutant SHP-1 constructs (DN1 and D61A) have been generated to mimic the open-form structure of SHP-1 as previously described . Antibodies for immunoblotting such as p-STAT3, STAT3, survivin, p-Akt, Akt, p44/42 MAPK (Erk1/2) (Thr202/Tyr204), ERK, p-VEGFR2, VEGFR2, p- mTOR, mTOR, p-JAK2, JAK2, poly (ADP-ribose) polymerase (PARP) and cleaved caspase 3 were ordered from Cell Signaling Technology (Danvers, MA, USA). SHP-1, cyclin D1, Mcl-1, Ki67, b-actin antibodies were purchased from Abcam (Cambridge, MA, USA). BCA Protein Assay Kit was purchased from Pierce (Rockford, IL, USA).
Human hepatocellular carcinoma cells HepG2, SK-Hep1, Hep3B2.1-7, Huh-7, and PLC-5 were obtained from the American Type Culture Collection (Manassas, VA) and cultured in Dulbecco’s Modified Eagle's Medium (DMEM; GIBCO, MD, USA), containing 10% (v/v) fetal bovine serum (FBS; GIBCO, MD, USA) at 37 °C in a 5% CO2- humidified incubator. All cell lines were authenticated by STR profiling using the AmpFISTR Identifiler PCR amplification kit (Applied Biosystems, Foster City, CA).
Establishment of Sor-resistant cells
Sorafenib-resistant cells HepG2SR and Huh7SR were established as described . In brief, two Sor-resistant HCC cell lines (HepG2SR and Huh7SR) were obtained by chronic exposure to Sor at low doses then increased to higher doses for a long period of time. Their ability of Sor resistance (SR) was further established and confirmed by incubating them with Sor at a starting concentration of 5 μM. Cells were continuously cultured with increasing concentrations of Sor by 1 μM per week for 1–2 months. The re-obtained SR-HCC cells were kept by culturing them in the presence of Sor.
All pathologic samples of patients were obtained following written informed consent. The protocol conforms to the ethical guidelines of the 1975 Declaration of Helsinki as reflected in a priori approval by the institution's human research committee.
Cell proliferation analysis
Cells were seeded in 96-well plate with 5,000 cells per well and were then treated with PH and/or Sor at indicated concentrations for 24, 48 and 72 h. After 24 h of incubation, 20 μl MTT (5 mg/ml) was added. The cultures were solubilized and the spectrophotometric absorbance was measured at 595 nm using a microtiter plate reader (Bio-Rad, USA). The number of viable cells was presented relative to untreated controls. The assay was repeated three times independently.
Colony formation assay
Colony formation assay was conducted as described previously . Briefly, HepG2SR and Huh7SR cells were seeded in 6-well plates (~1000-5000 cells per well) and treated with PH (50 μM). After incubation for 48 h, the cells were washed by PBS and then cultured in normal medium for two weeks. At the end of time point, cells were washed in PBS, fixed with 100% methanol and stained with a filtered solution of crystal violet (5% w/v). Colonies were visualized by Nikon Eclipse TS100 inverse microscope (Nikon Corporation, Japan) and pictures were captured using Nikon E8400 camera.
Cytoplasmic histone-associated DNA fragments were determined by the measurement of apoptotic cells using the Cell Death Detection ELISAPLUS Kit Roche (Indianapolis, IN) according to the manufacturer's instructions.
Approximately 2×105 cells/well seeded in 6-well plates were treated with varying concentrations of PH for 48 h. Thereafter, the cells were collected and washed twice in ice-cold PBS before incubated with 5 μL FITC-Annexin V and 5 μL propidium iodide (PI) at room temperature for 15 min in the dark. Apoptotic cells were detected using an Annexin V-FITC Kit (BD Pharmingen, Franklin Lakes, NJ, USA) according to the manufacturer’s protocol. All samples were analyzed immediately using FACSCalibur flow cytometer (BD, San Jose, CA).
Measurement of caspase-3, -8 and -9 activities
Caspase-3, -8 and -9 colorimetric Assay kits (BioVision, Inc.) were utilized as an additional method to evaluate apoptosis. The results are expressed as relative caspase-3, -8 and -9 activation in cells exposed to PH or Sor or both.
HCC with ectopic STAT3 expression
STAT3 cDNA (KIAA1524) was purchased from Addgene plasmid repository (http://www.addgene.org). HepG2 and SK-Hep1 cells with ectopic expression of STAT3 derived from a single stable clone were exposed to PH. Briefly, following transfection, cells were cultured in the presence of G418 . After eight weeks of selection, surviving colonies arising from stably transfected cells were selected and individually amplified.
Gene knockdown using siRNA
siRNAs targeting STAT3 and AKT with scrambled control siRNAs were purchased from Dharmacon (Thermo Scientific, Chicago, IL, USA). Cells were transfected with siRNAs using Lipofectamine 2000 (Invitrogen Life Technologies, MD, USA) to knockdown gene expression as described previously .
SHP-1 Phosphatase activity
SHP-1 activity was determined by using a RediPlate™ 96 Enzchek™ Tyrosine Phosphatase Assay Kit (Thermo Scientific, Chicago, IL, USA) according to the manufacturer's instructions.
Phospho-Stat3 (Tyr705) Sandwich ELISA Kit (Cell Signaling Technologies) was used to measure p-STAT3 activity according to the manufacturer's instructions.
Cells or the isolated independent tissues were lysed with RIPA Lysis Buffer (Santa Cruz Biotechnology, CA, USA) containing protease inhibitor (Roche Corp., Basal, Swiss) and phosphatase inhibitor (Roche Corp., Basal, Swiss) as described previously . The proteins were separated by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS–PAGE) and transferred to polyvinylidene difluoride (PVDF) membranes. The membranes were then incubated with primary antibodies overnight at 4°C followed by secondary antibodies for 1h at room temperature. Protein bands were visualized with enhanced chemiluminescence.
Real-time reverse transcription PCR
Total RNA was extracted from tumors using TRIzol (Invitrogen) and RNeasy Mini Kit (Qiagen) and subsequently reverse-transcribed to cDNA using the SuperScript Kit (Invitrogen). Quantitative PCR (qPCR) was carried out on the MX3000P real-time PCR system (Stratagen, USA). The amplification specificity was confirmed by the melting curves. Relative mRNA levels were calculated based on the Ct values and normalized using β-actin expression, according to the equation: 2−ΔCt [ΔCt = Ct target gene-Ct β-actin]. All experiments were performed in triplicate.
To investigate whether PH has a therapeutic effect on tumorigenesis in vivo, HepG2 (2 × 106) and SK-Hep1 (3 × 106) cells were injected SC inoculated into the posterior flank of nude mice and treated IP with PH 5 times a week for 3 weeks. Further to extrapolate our in vitro results to in vivo, we injected HepG2SR (3 × 106) and Huh7SR (5 × 106) cells in mice which received daily oral Sor at 10 mg/kg, which was used to maintain the Sor-resistant capacity of both HepG2SR and Huh7SR cells in mice . When tumors became palpable ~100 mm3, animals were randomly divided and received PH, Sor or both. Tumor volume (TV) was calculated as follows: TV = (L × W2)/2 every third day till the animals were sacrificed and tumor weights were measured on day 30 after tumor excision. Survival rate was evaluated by the Kaplan–Meier method. Mice of each group were also monitored for other symptoms of side effects including food and water withdrawal and impaired posture or movement. At the termination of the experiment, the tumor tissues were harvested and used for immunohistochemistry. All procedures for animal experimentation used in the current study were approved by the Institutional Animal Ethics Committee, King Saud University, Riyadh, Saudi Arabia.
In brief, 5 μm-thick paraffin-embedded tumor sections from nude mice were stained for CD31, pSTAT3, Caspase-3, TUNEL and Ki67 using standard immunostaining protocols  and scanned at ×200 magnification. Six fields per section were analyzed and the expression levels of the target markers were semi-quantitatively assessed based on staining intensity by a board-certified pathologist.
Molecular docking with SHP-1
SHP-1 was downloaded from RCSB PDB using pdb id: 3PS5. The protein was first prepared and the active sites were predicted using Discovery studio. his protein was then used for docking purpose using Autdock Vina [31, 32, 33]. Further, PH was docked with AKT1(4EJN). Each crystal structure of mentioned proteins was co-crystallized with a ligand bound at ATP binding site. Centre of mass of each bound ligand was calculated and utilized during molecular docking simulation. AutoDock vina program [31, 32, 33] was used for molecular docking and calculating the binding score of bound ligands of the proteins. Ligand efficacy (LE) of PH and other ligands was calculated as described by Hopkins et al . UCSF Chimera and Ligplot programs were used for visualizing, editing and analysis of ligand and proteins interactions [35, 36].
Statistical analysis was performed with GraphPad Prism (GraphPad Software, San Diego, CA). Student’s t test was used to evaluate statistical significance of differences between two groups and p < 0.05 was considered statistically significant. Measurement values were expressed as mean ± SD.
PH possesses anticancer and apoptotic effects in HCCs and potentiates Sor efficacy
To investigate the anticancer effects of PH against hepatic carcinoma, we first assessed growth inhibition in response to PH, in a panel of five HCC cell lines: SK-Hep1, Hep3B2.1-7, Huh7, PLC5, and one human hepatoblastoma cell line HepG2. Cell viability was determined by MTT assay after treatment for 24, 48 and 72 h. As shown in (Fig. 1c), PH significantly reduced cell viability in a concentration- and time-dependent manner. Next, we examined the apoptotic effect of PH on HCCs. PH alone significantly increased the activation of caspase-3, 8 and 9 in HepG2 and SK-Hep-1 cells as observed with colorimetric assay (Bio Vision, USA) (Additional file 1: FigureS1A). Importantly, inhibition of cellular growth and activation of apoptosis by PH were associated with a significant induction of DNA fragmentation in a concentration-dependent manner in all the five HCC cell lines (Fig. 1d). To further explore the mechanism of cell death mediated by PH in HCCs, we first measured the degree of cell apoptosis using Annexin V/PI staining. PH alone increased the percentage of HCC cells underwent apoptosis (Annexin V+/ PI+ population), a biomarker of apoptosis, in a concentration-dependent manner (Fig. 1e). Second, we studied the effect of PH on caspase-3 cleavage, where we found that PH induced the activation of caspase-3 cleavage and increased cleavage of poly (ADP- ribose) polymerase in all HCC cell line tested (Fig. 1f).
To answer the question of whether PH could enhance the cancer activity of Sor, we tested the effect of PH and Sor combination on cell proliferation and apoptosis in several HCC cells. Our results showed that Sor or PH alone decreased cell proliferation of HepG2, SK-Hep1, Hep3B2.1-7 cells in a concentration-dependent manner, whereas combination of Sor and PH significantly potentiated the suppression of the cell proliferation (Additional file 2: FigureS2A), while significantly increased the apoptosis as observed by Annexin V and DNA Fragmentation assays (Additional file 2: Figure S2B, S2C). These data not only indicate that PH inhibits HCC cell proliferation through induction of apoptosis but also shed the light on its synergistic effect on the antitumor activity of Sor.
To explore the role of STAT3 and SPH-1 in the anticancer activity of PH, two independent experiments were conducted. First, we measured the effect of combination therapy on p-STAT3 and SHP-1 activities. Our results showed that PH in combination with Sor markedly decreased the p-STAT3 (Additional file 2: Figure S2D, S2E) while enhanced SHP-1 (Additional file 2: Figure S2F) activities as compared to monotherapy. Second, we next examined whether knockdown of STAT3 and Akt by siRNAs could potentiate the anticancer activities of PH in HCC cells. For this purpose, HepG2 and SK-Hep1 cells were transfected with control, STAT3 siRNA or Akt siRNA for 24 h and then further combined for 48 h with PH (Additional file 3: Figure S3A, S3B). Our results show that knockdown of both STAT3 and Akt by siRNA induced apoptosis in both cells, suggesting that PH inhibits Sor-induced STAT3 and Akt activation, thus reversing Sor resistance in HCCs.
PH induced HCC cell death via inhibiting STAT3/AKT/ERK signaling
To further validate the role of STAT3 in PH-induced apoptosis, we generated stable STAT3-overexpressing HepG2 and SK-Hep1 and tested the molecular changes induced by PH treatment. Ectopic expression of STAT3 increased p-STAT3 protein expression (Fig. 2d) and decreased the percentage of apoptotic cells (Fig. 2d), suggesting that activated STAT3 signaling counteracts the apoptotic activity of PH in HCCs. To tested whether these in vitro results are extrapolated into human model, we performed immunohistochemistry (IHC) assay to examine the levels of CD31, SHP1 and pSTAT3 in liver tissues obtained from healthy and HCC patients. IHC staining shows strong SHP-1 correlation with p-STAT3 expression in normal liver and vice versa in human tumor samples (Fig. 2e).
PH increased SHP-1 phosphatase activity by direct interaction
To further validate the role of SHP-1 in PH-mediated molecular events and apoptosis, we tested whether inhibition of SHP-1 either chemically using a specific inhibitor (PTP III) or genetically via transient transfection of SHP-1-targeted siRNAs would alter PH effects in HCC cells. Our results showed that blocking of SHP-1 either using PTP III (Fig. 3d) or siRNA (Fig. 3e) abolished PH-mediated cell death and downregulation of p-STAT3 in both HepG2 and SK-Hep1 cells. PH induced significant cell death and inhibition of STAT3 in HepG2, SK-Hep-1 and Hep3B2.1-7 cells overexpressing SHP-1 (Fig. 3f). This data suggests that PH increases SHP-1 activity by direct interaction that subsequently results in SHP-1–mediated inhibition of p-STAT3.
PH interfered with inhibitory N-SH2 domain and relieved autoinhibition of SHP-1
To investigate the mechanism through which PH increased SHP-1 tyrosine phosphatase activity, we transfected HepG2 and SK-Hep1 cells with wild-type or mutant SHP-1 (dN1 and D61A), thereafter we examined the effect of PH on SHP-1. The intramolecular inhibition of SHP-1 is protected by various biochemical associations between N1 and PTP catalytic domain, such as Asp61 and Lys362 (salt bridge) . Deletion of the autoinhibitory N-SH2 domain (dN1) and single-mutant D61A of SHP-1 was used to mimic the open-form structure of SHP-1. PH co-incubated with purified wild-type or mutant SHP-1 proteins in vitro enhanced the activity of wild-type SHP-1 protein to nearly 2.6 and 2-folds in HepG2 and SK-Hep1 cells, respectively (Fig. 3g). As compared to Sor, sc-43 and sc-60, PH increased the phosphatase activity in recombinant SHP-1 proteins expressing dN1 or D61A mutants in both HepG2 and SK- Hep1 cells. In addition, wild-type SHP-1–transfected HCC cells showed a marked decrease in p-STAT3Tyr705 level (Fig. 3i) and a significant increase in apoptosis (Fig. 3h, Additional file 2: Figure S2G). Whereas no such effect was observed in dN1 or D61A mutant SHP-1–transfected HCCs (Fig. 3i). These findings suggest that PH activates SHP-1 by disruption of autoinhibition of SHP-1, leading to reduced p-STAT3Tyr705 level and eventual induction of apoptosis in HCC cells (Fig. 3j). Thus, SHP-1 targeting is critical in PH-induced anti-HCC activity.
PH overcome Sor resistance in HCCs
Sor-resistant cell lines HepG2SR and Huh7SR were used to study whether PH could overcome the resistance in HCC cell lines and whether p-STAT3 and SHP-1 are involved. Resistance of HepG2SR and Huh7SR cells to Sor has been confirmed by the significant decrease in growth inhibition (Additional file 4: Figure S4A), no significant changes on p-STAT3 protein expression and percentage of apoptotic cells (Additional file 4: Figure S4B), no induction of DNA fragmentation in both resistant cells (Additional file 4: Figure S4C). These results clearly suggest that Sor-resistant cells become refractory to Sor-induced apoptosis.
PH overcome STAT3-, AKT-, MAPK- and VEGFR2-dependent resistance to Sor in HCCs
To further explore the mechanisms of PH effect on Sor-resistant HCC cells, we investigated the effect of PH on the protein expression and activity of p-STAT3 and SHP-1 in Sor-resistant HepG2SR and Huh7SR cells. PH treatment resulted in downregulation of p-STAT3 protein expression and its targets in a concentration-dependent manner (Fig. 4d) with significant decrease in p-STAT3 activity at 50 and 100 μM concentrations using ELISA (Fig. 4e). With regards to SHP-1, PH treatment caused marked increases in SHP-1 activitiy (Fig. 4f) and mRNA (Fig. 4g) levels in both HepG2SR and Huh7SR cells.
STAT3 has been reported to be activated by JAK2 , therefore, we test the effect of PH on JAK2. Our results showed that PH inhibited phosphorylation of JAK2 in a concentration-dependent manner in Sor-resistant cells (Fig. 4d). Previous study has shown that Sor-induced Akt, ERK and VEGFR2 activation has been reported in both Sor-resistant and parental HCC cells [3, 4, 11] and that increased p-Akt, p-ERK and p-VEGFR2 expression is responsible for resistance to Sor. We next examined alterations of the key molecules in the Akt/mTOR, MAPK and VEGFR2 pathways, pathways that have been shown to be responsible for resistance to Sor . Our results showed that Sor-resistant cells expressed higher levels of p- Akt, p-ERK and p-VEGFR2 resulting in upregulation of p-mTOR (Fig. 4d). Importantly, PH treatment downregulated p-Akt, p-ERK, p-VEGFR2 and p-mTOR protein expression in a concentration-dependent manner but did not affect the total protein expression (Fig. 4d).
To further investigate the mechanism through which PH increased SHP-1 and decreased p-STAT3 in Sor-resistant cells, we knocked down SHP-1 using siRNA to address whether SHP-1 is mediating Sor resistance. As shown in Fig. 4h, while PH treatment increased SHP-1 and repressed p-STAT3 proteins with inhibition of colony formation, SHP-1 silencing abolished the inhibitory effects of PH on p-STAT3 and colony formation in Sor-resistant cells. These results not only indicate the critical role of SHP-1 in PH-induced inhibition of cell growth, but also suggest that targeting SHP-1 by PH could overcome Sor resistance.
PH combination with Sor synergizes the antitumor effect in SR-HCCs
PH inhibited tumor growth via a SHP-1/STAT3-related signaling pathway in vivo
Angiogenesis plays important role in tumor growth, progression and metastasis . Therefore, we examined whether PH inhibits angiogenesis in vivo. Immunostaining with CD31 markedly decreased angiogenesis in tumor tissues in both HepG2 (Fig. 6g) and SK-Hep1 (Additional file 5: Figure S5A) xenografts treated with PH in a dose-dependent manner. Significant decrease in p-STAT3 expression in both HepG2 (Fig. 6g) and SK-Hep1 (Additional file 5: Figure S5F) xenografts was observed. TUNEL labelling and caspase-3 expression revealed a high induction of apoptosis by a factor of 9 and 10 in HepG2 (Fig. 6g) and 8 and 11 in SK-Hep1 (Additional file 5: Figure S5F) with PH 50 mg/kg. There was a significant decrease in Ki67+ cells in PH treated tumors (Fig. 6g; Additional file 5: Figure S5F). These results suggest that PH inhibits tumor growth by impairing angiogenesis, cell proliferation and inducing apoptosis in both HepG2 and SK-Hep1 tumors.
Further, we tested the combined effect of PH and Sor on the tumor volume in both HepG2 and SK-Hep1 xenografts. PH (50 mg/kg) alone decreased the tumor volume by 75% and 71%, whereas Sor alone (20 mg/kg) decreased the tumor volume by 54% and 51% in HepG2 and SK-Hep1 xenografts, respectively (Additional file 5: Figure S5A). Importantly, combination therapy of PH and Sor produced an additive decrease in tumor volume by 83% and 89% in both cells, respectively (Additional file 5: Figure S5A). However, no significant changes in body weight loss or other clinical signs of toxicity were observed in any groups (Additional file 5: Figure S5B). Further we examined whether the potentiation effect of combined therapy of PH and Sor on tumor volume is associated with synergistic effect on SHP-1 and p-STAT3. Additional file 5: Figure S5D shows that a synergistic increase in SHP-1 activity with a further decrease in p-STAT3 activity and downstream proteins as compared to monotherapy. No histological differences were observed in various organs between the control and PH treated groups (Additional file 5: Figure S5C). These results suggest that PH acts as a potent STAT3 inhibitor and SHP-1 enhancer, and thus induces its anti–hepatocellular carcinoma effect via a STAT3-related signaling pathway.
PH possessed antitumor effect against Sor-resistant xenograft tumors
We further investigated the effect of PH, Sor or combination treatment on SPH-1 and p-STAT3 expression in HepG2SR and Huh7SR xenografts. In consistency with the in vitro and in vivo results, Western blot assay results showed a significant decrease in p-STAT3 protein expression and its downstream targets (Fig. 7c) and an increase in SHP-1 activity (Fig. 7d). In addition, immunostainings for CD31, p-STAT3, caspase-3 and ki67 showed that Sor had a weak inhibitory effect on cell proliferation with weak pro-apoptotic activity against Sor-resistant tumors (Fig. 7e), whereas, PH significantly decreased CD31, p-STAT3 and Ki67 expression while induced caspase-3 activity in both HepG2SR and Huh7SR xenografts. These Inhibitory effects were also observed in combination with Sor but is not significant as compared to PH alone. Together, our data indicate that PH inhibited the tumor growth both in vitro and in vivo through a STAT3 inhibition mechanism involving SHP-1.
Over-expression and hyperactivation of STAT3 has been reported in various human tumors. STAT3 and MAPK play an important role in signal transduction cascades, which take part in cellular physiological growth, development, mitogenesis and differentiation, and cellular malignant transformation . One of the novel strategies to prevent sustained STAT3 over-expression in cancer cells is through the activation of intrinsic regulators such as SHP-1 . This effect is supported by the findings of several studies revealed that loss of SHP-1 leads to constitutive activation of STAT3. In addition, SHP-1 has been shown to dephosphorylate STAT3 directly to silence the JAK/STAT pathway . The current study provides the first evidence that PH demonstrates a significant anti-proliferative effect in HCCs via STAT3 pathway inhibition. Our data suggest that PH inhibits the JAK/STAT3 signaling pathway by stimulating Tyr705 dephosphorylation of STAT3 and inhibiting p-JAK2. PH also upregulates SHP-1 activity and induces SHP-1-dependent p-STAT3 downregulation.
Activation of the AKT/mTOR and RAS/MAPK cascades is frequently observed and associated with aggressive tumor phenotypes and poor prognosis in human HCC . SHP-1 is a negative regulator of the cell cycle, as well as inflammatory and JAK/STAT pathways in cancer progression . We have observed that PH significantly decreased expression of p-ERK p-Akt and p-mTOR in all tested HCCs. Inhibiting SHP-1 using specific inhibitor, PTP inhibitor III, upregulates p-STAT3 and rescues the SC-43-induced apoptosis. The antiproliferative activity of PH was significantly counteracted by SHP-1 knockdown using siRNA suggesting that PH mainly targets SHP-1 and downregulates p-STAT3, and thus inhibits cell proliferation and induces apoptosis. The dN1 mutant showed slight increase in SHP-1 activity in both HCCs, but it was not significant, whereas D61A mutants demonstrated a significant increase in SHP-1 activity only in HepG2 not in SK-Hep1 indicating that D61 site of the inhibitory N-SH2 domain is crucial for PH-induced SHP-1 upregulation, although it behaves differently in HepG2 compared to SK-Hep1 cells. This could be explained by its flexible orientation and unknown mechanism for searching of phospho-tyrosine activators . PH-induced downregulation of p-STAT3 was found in HCCs cells expressing wild-type (WT) of SHP-1. However, ectopic expression of dN1 and D61A restored the expression of p-STAT3. Together, the data suggest that PH may affect SHP-1 by switching the confirmation from autoinhibitory (closed) to active (open). Our in vivo studies recaptured our findings in vitro, that PH showed significant antitumor activity via inhibition of p-STAT3 and upregulation of SHP-1 activity in HCC- xenografts and improved the overall survival.
In summary, our study demonstrated the preclinical activity of PH, which inhibits hepatic carcinoma in vitro and in vivo and prolonged mouse survival via molecular targeting of STAT3/Akt/mTOR/JAK2/VEGF2 pathways. PH holds promise as an adjuvant drug for HCC treatment and is equally as potential as Sor. This may represent an alternative strategy in the treatment of HCC.
The publication of this article was funded by the Qatar National Library, Qatar. The graphical abstract was created with BioRender.com
SS and AA generated the idea, designed the experimental protocol designed study. SS acquired, analyzed and interpreted data; performed statistical analysis and wrote the manuscript. AGM and HMK drafted and revised the manuscript. PT performed docking studies. All authors read and approved the final manuscript.
College of Medicine and Pharmacy Research Centers and Deanship of Scientific Research, King Saud University, Riyadh, Saudi Arabia.
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There are no financial or other interests with regard to this manuscript that might be construed as a conflict of interest. All of the authors are aware of and agree to the content of the manuscript and their being listed as an author on the manuscript.
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