The natural polyphenol curcumin induces apoptosis by suppressing STAT3 signaling in esophageal squamous cell carcinoma
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We and others have previously shown that the STAT3 signaling pathway is activated in some esophageal squamous cell carcinoma (ESCC) cells and is required for the survival and growth of these primary ESCC-derived xenografts. It has also been shown that the natural polyphenol curcumin is an effective anti-tumor agent.
Luciferase assay and immunoblotting were performed to examine whether curcumin suppressed STAT3 signaling. CCK-8 assay and xenografts were utilized for analyzing ESCC cell growth in culture and mice. Soft agar assay was carried out to determine the colony formation ability of ESCC cells in the presence or absence of curcumin. Cell death and cell cycle were assessed by In CELL Analyzer 2000. Immunohistochemistry and TUNEL assay were used for detecting apoptosis in ESCC tisuses. Molecular docking was performed to evaluate the interaction of curcumin with JAK2. JAK2 activity was assessed using an in vitro cell-free system. HE staining was used to evaluate the ESCC tissues.
The natural polyphenol curcumin inhibited STAT3 phosphorylation rapidly and blocked STAT3-mediated signaling in ESCC cells. It also induced growth arrest and apoptosis in cultured ESCC cells, which were attenuated by enforced expression of STAT3. Furthermore, curcumin preferentially blocked the growth of primary ESCC-derived xenografts that harbored activated STAT3.
Curcumin is able to exert anti-tumor action through inhibiting the STAT3 signaling pathway. Giving its wide use in traditional medicines with low toxicity and few adverse reactions, it is conceivable that curcumin might be further explored as a unique STAT3 inhibitor for anti-cancer therapies.
KeywordsCurcumin STAT3 Esophageal squamous cell carcinoma Apoptosis PDX model
Cell Counting Kit-8
Esophageal squamous cell carcinomas
- HE staining
Janus kinase 2
Quantitative real-time polymerase chain reaction
Sodium dodecylsulfate polyacrylamide gel electrophoresis
Signal transducer and activator of transcription 3
Tumour necrosis factor alpha
Terminal dexynucleotidyl transferase(TdT)-mediated dUTP nick end labeling
Esophageal cancer is the eighth most common malignancy and the sixth most common cause of death from malignancy worldwide . Esophageal squamous cell carcinoma (ESCC) is the most common type of esophageal cancers and accounts for 90% of the cases, whose 5-year survival rate remains less than 30% . The development of ESCC is a multifactorial, multistage and complex biological process involving multiple gene abnormalities . As early as 1850s, Virchow found that inflammation was associated with cancers . Recent studies demonstrated that inflammation could initiate and promote malignant transformation, whereas the genetic and epigenetic changes of malignant cells could generate the inflammatory microenvironment to further support the progression of the tumor . Noteworthily, large number of studies have shown that inflammation-related smoking, alcohol, diet and human papilloma virus (HPV) are all associated closely with the development of ESCC .
Curcumin is the main natural polyphenol found in the rhizome of Curcuma longa (turmeric). Many studies showed that curcumin has anti-oxidation, anti-growth, antiarthritic and anti-inflammation actions . In particular, it has been reported that curcumin induces apoptosis, inhibits cell proliferation and migration in human leukemia, colon, prostate, renal and non-small-cell lung cancer [7, 8, 9], suggesting that it might be a novel agent for the prevention and treatment of ESCC.
The Janus kinase/signal transducers and activators of transcription (JAK/STAT) pathway plays an essential role in immune response, inflammation, and carcinogenesis [10, 11]. Cytokines bind to the receptors and activates JAKs, which in turn phosphorylates STATs. Dimerized and phosphorylated STATs are then translocated into the nucleus to regulate gene expression. Some of these genes are important in cell proliferation and survival, including cyclins and anti-apoptotic proteins . In particular, STAT3 can be activated in many cells by various cytokines and growth factors, such as IL-6 and EGF family members [13, 14]. Noteworthily, constitutive activation of STAT3 has been found in various human cancers, such as breast cancer, prostate cancer, ovarian cancer, hepatocarcinoma, and it has shown that activation of STAT3 contributes to tumor cell growth, metastasis and angiogenesis [15, 16, 17, 18]. Thus, targeting STAT3 is regarded as a promising strategy for developing novel therapeutics.
In this study, we used ESCC cell lines and four ESCC PDX (patient-derived xenograft) models to further explore the activity and mechanism of curcumin. We found that the compound downregulates STAT3 signaling by suppressing JAK2 activation, leading to inhibition of cell growth and clony formation, cell cycle arrest and apoptosis. Furthermore, preventive use of curcumin significantly inhibited tumor growth in ESCC patient-derived xenografts. These results indicated that curcumin is an effective agent for the preventive treatment of ESCC harboring constitutively activated STAT3.
Materials and methods
Cells, tissues and chemicals
Esophageal squamous cell carcinoma (ESCC) cell lines EC1, EC9706, KYSE450 and TE13 were provided by Department of Pathophysiology, School of Basic Medicine, Zhengzhou University. All ESCC cell lines were cultured in Dulbecco’s high glucose modified Eagle’s medium (DMEM) supplemented with 10% fetal bovine serum (FBS), 100 μg/ml of penicillin, and 100 units/ml of streptomycin at 37 °C with 5% CO2.
The ESCC tumors used for this study were collected from patients enrolled into the First Affiliated Hospital of Zhengzhou University (Zhengzhou, China) with consensus, and approved by the Ethics Committee of Zhengzhou University. None of these patients had received preoperative chemotherapy or preoperative radiation therapy. The fresh tumor specimens were collected at the time of surgical resection and prepared for implantation in immunodeficient mice. All specimens were examined by two pathologists to confirm the malignant tissues. All the tissues were inoculated into the mice within 2 h after the operations.
Curcumin, Z-VAD-FMK and AG490 were purchased from Selleck Chemicals (Houston, TX, USA). Annexin V-FITC Apoptosis Detection Kit was purchased from Beyotime Biotechnology (Shanghai, China).
Plasmids construction and gene transfection
The human STAT3 cDNA was cloned into pcDNA3.1 vector with a Myc tag as previously described [19, 20]. A STAT3 luciferase construct (STAT3-Luc) was purchased from Beyotime Biotechnology (Shanghai, China). Plasmids were transiently transfected into EC9706 or TE13 cells by Lipofectamine® 2000 (Invitrogen) according to the manufacturer’s instruction.
After transfected with STAT3-Luc or empty vector along with the internal control renilla luciferase by Lipofectamine® 2000 (Invitrogen) for 24 h, TE13 cells were incubated with indicated agents for 12 h, and then stimulated with 50 ng/ml IL-6 (Novoprotein, Shanghai, China) or vehicle control for 20 min. Cells were then prepared for luciferase assay by using Dual-Luciferase® Reporter Assay System (Promega, Madison, WI, USA) as described previously [21, 22].
Whole cell lysates were prepared for immunoblotting as described previously [23, 24, 25]. Equal amounts of total proteins (30 μg) were subjected to SDS-PAGE, transferred onto nitrocellulose, and immunoblotted with specific antibodies. The primary antibodies against phospho-STAT3 (Tyr705), STAT3, phospho-JAK2 (Tyr1007/1008), JAK2, PARP, MCL1, XIAP, Cox2 and iNOS were purchased from Cell Signaling Technology (Danvers, MA). Anti-β-Actin, anti-α-Tublin, anti–mouse IgG and anti–rabbit IgG horseradish peroxidase conjugated antibodies were purchased from Santa Cruz (Santa Cruz, CA). Anti-Myc antibody was purchased from Medical & Biological Laboratories (Tokyo, Japan). Anti-GAPDH antibody was purchased from Abgent (Suzhou, China).
Cell survival analysis
ESCC cells were seeded in 96-well plates at a density of 5000 cells/100 μl and cultured overnight at 37 °C with 5% CO2. After treated with indicated concentrations of curcumin for different times, their survival was measured by CCK-8 assay according to the manufacturer’s protocol as described previously . Absorbance was measured at 450 nm wavelength.
Colony forming assay
The colony forming assay was performed as described previously . EC9706 cells (2.4 × 104/well) were exposed to various concentrations of curcumin in BME agar with 10% FBS, and then cultured for 2 or 3 weeks at 37 °C in a 5% CO2 incubator. Colony numbers were determined by a microscope using Image-Pro Plus software (Media Cybernetics, Inc. Rockville, MD).
Cell cycle and apoptosis analyses
Cell cycle and apoptosis analyses were performed as described previously [25, 26]. EC9706 (1 × 104/well) were seeded in 96-well plates and incubated overnight, and treated with different doses of curcumin (0, 4, 8, 12, 16 μM) for 24 h. For apoptosis detection, the cells were stained with Hoechst (Beyotime, Shanghai, China) and Annexin V–FITC Kit (Beyotime, Shanghai, China). For cell cycle analysis, the curcumin-treated cells were fixed with 4% paraformaldehyde and stained with DAPI (Solarbio, Beijing, China) according to the protocol and protected from the light for 20 min at 37 °C in a 5% CO2 incubator. They were analyzed by In CELL Analyzer 2000.
Quantitative real-time polymerase chain reaction (qRT-PCR)
Total RNA was extracted using RNAiso Plus (Takara Bio Group, Japan) according to the manufacturer’s instructions. cDNA was synthesized from equal quantities of total RNA using the PrimeScriptTM RT reagent Kit with gDNA Eraser (Takara Bio Group, Japan). To determine the mRNA levels of Cyclin D1, MCL1 and IL-6, qRT-PCR was performed using SYBR Green qPCR Master Mix (Clontech Laboratories, Inc., USA) with Roche LightCycler® 480II real-time PCR system (Roche, Basel, Switzerland). The primers used were as follows: Cyclin D1, forward 5’-AGCTGTGCATCTACACCGAC-3′ and reverse 5’-GAAATCGTGCGGGGTCATTG-3′; MCL1, forward 5’-GCGACGGCGTAACAAACT-3′ and reverse 5’-ACCCATCCCAGCCTCTTT-3′; IL-6, forward 5’-GTCCAGTTGCCTTCTCCC-3′ and reverse 5’-GCCTCTTTGCTGCTTTCA-3′; GAPDH, forward 5’-GCACCGTCAAGGCTGAGAAC-3′ and reverse 5’-TGGTGAAGACGCCAGTGGA-3′.
The CDOCKER module of Discovery Studio 3.5 (DS3.5) was used for molecular docking . The crystal structure of JAK2 (PDB entry: 5TQ8)  from the RCSB Protein Data Bank (http://www.rcsb.org) was used as the initial structure for molecular docking. The protein structure was prepared with the Prepare Protein tool in DS3.5 and curcumin was sketched by using DS3.5 and then prepared with the Prepare ligands tool. All parameters were set to default. After preparation of the protein and the compound, curcumin was docked into the active site of JAK2, and all parameters were set to default in the docking process of CDOCKER, the protein conformation was fixed and the docked ligand was flexible.
Protein kinase activity assay
Patient-derived xenograft (PDX) study
The human ESCC PDX model was established in female CB17/SCID mice (Vital River, Beijing, China). The primary tumors that had passed 3 generations of implantations were inoculated subcutaneously. When the tumors became palpable, the mice were divided into the following four groups (n = 8/group): (a) control vehicle (80% DMSO + 20% PBS); (b) curcumin prevention and treatment (Mice were in advance intraperitoneally injected with 100 mg/kg curcumin three times a week for half a month before the formal experiment; 100 mg/kg); (c) curcumin (100 mg/kg); (d) 5-FU(5 mg/kg). Curcumin was intraperitoneal injected three times a week for 4 weeks, and 5-FU was injected continuously for the first 3 days. Body weights and tumors were measured twice a week. Tumors’ volume was calculated as length × width2 × 1/2. The study was approved by the Ethics Committee of First Affiliates Hospital of Zhengzhou University and Basic Medical College of Zhengzhou University.
The paraffin embedding tissue sections were deparaffinized in xylene, treated with a graded series of alcohol and distilled water, and washed thoroughly with TBST. Antigen was retrieval with 0.01 M sodium citrate (pH 6.0) and microwave boiling. Endogenous peroxidase was blocked by using H2O2. After throughly washing with TBST, the slides were incubated overnight at 4 °C with primary antibodies: p-STAT3, Cox-2 and Caspase-3 diluted in 5% BSA-TBST (1:50) respectively. They were then incubated for 15 min with appropriate dilutions of the secondary antibody at 37 °C for 15 min, and were visualized by incubating with DAB for ~ 5 min. All sections were examined under microscope and analyzed using the HistoQuest 4.0 (TissueGnostics, Austria) as described previously .
The paraffin embedding tissue sections were deparaffinized in xylene, treated with a graded series of alcohol and distilled water, and washed thoroughly with PBS. They were then incubated with proteinase K (20 μg/ml in PBS) for 20 min at room temperature, and TUNEL staining was carried out using the in Situ cell death detection kit (KeyGen Biotech Ltd., Nanjing, China) according to the manufacturer’s instructions. TUNEL-positive cells from five independent fields were counted manually.
The results were expressed as mean ± standard deviation (S.D), except otherwise stated. The datas were analyzed by one-way analysis of variance or Student t test, using SPSS version 17.0 (SPSS, Chicago, USA). p < 0.05 was considered statistically significant.
Curcumin inhibited the growth of ESCC cells
Curcumin promoted cell cycle arrest and induced cell apoptosis in ESCC cells
Curcumin inhibited STAT3 activation by suppressing JAK2 phosphorylation in ESCC cells
Curcumin suppressed tumor growth in ESCC PDX models
The clinical pathological features of PDXs
oesophagus squamous cell carcinoma
oesophagus squamous cell carcinoma
oesophagus squamous cell carcinoma
oesophagus squamous cell carcinoma
Curcumin suppressed STAT3 phosphorylation and induced apoptosis in ESCC PDX models
STAT3 can be activated by a variety of cytokines including IL-6, IL-10 and TNFα . Constitutive activation of STATs has been found in a number of tumors, including lymphoma, breast cancer, colorectal cancer and prostate cancer [32, 33, 34, 35]. Many of the physical, chemical and biological stimuli that induce inflammation, including ultraviolet, reflux gastric juice, and endotoxin, can also activate STAT3 by different mechanisms . Moreover, genes induced by STAT3 can also promote the development of inflammation, forming the positive feedback mechanisms of inflammation development . It has been shown that STAT3 is an important regulator for many genes involved in survival, invasion, cycling, and apoptosis of tumor cells [39, 40]. It has been also demonstrated that down-regulation or inhibition of STAT3 signaling can suppress tumor growth in vitro and in animal models . Thus, STAT3 appears to be a desirable drug target for cancer therapy.
Curcumin is a yellow pigment commonly used as a dietary spice and as a component of tranditional medicine in China and India, primarily for anti-neoplasms and anti-inflammation . Although the compound has not been developed as a drug in modern medicine, it is conceivable that identification of proper biomarkers, such as activated STAT3, might significantly promotes its clinical trials and potential applications in the not-so-distant future. Whasun Lim et al.  found that curcumin suppressed proliferation and migration, and induced apoptosis on human placental choriocarcinoma. Gallardo et al.  also showed that curcumin inhibited invasive capabilities of breast cancer cells. Our previous study demonstrated that NF-κB signaling pathway was activated in a subgroup of esophageal squamous cell carcinoma (ESCC), and curcumin inhibited ESCC cell proliferation and induced apoptosis [45, 46, 47]. Therefore, exploring the effect of curcumin on STAT3 signaling may provides novel therapeutic strategies for ESCC.
In this study, we found that curcumin inhibited the growth of different ESCC cell lines (Fig. 1). It induced cell cycle arrest at S phase and promoted apoptosis dose-dependently in EC9706 and TE13 cells (Fig. 2). Both constitutive and IL6-induced STAT3 activations were strongly inhibited by curcumin treatment in EC9706 and TE13 cells (Fig. 3). Noteworthily, Cox2, which catalyzes the conversion of arachidonic acid to prostaglandins, is inducible by many cytokines in an STAT3-dependent manner [48, 49]. It is highly expressed in many premalignant and malignant lesions, including nasopharyngeal carcinoma, lung cancer, breast cancer [50, 51, 52]. A number of studies indicated that Cox2 plays an important role in apoptosis, angiogenesis and tumor invasion . In the present study, we found that the expression of Cox2 was markedly inhibited by curcumin in PDX of ESCC (Fig. 6e-h). We also found that overexpression and activation of STAT3 all decreased the sensitivity of ESCC cells to curcumin (Fig. 2e-g), and the STAT3 inhibition enhanced curcumin-induced ESCC cell death (Fig. 2h). Thus, the effect of curcumin on ESCC cells requires the inhibition of STAT3-mediated signaling.
In the animal experiments, we evaluated the potential therapeutic as well as chemopreventive action of curcumin. Interestingly, as shown in Fig. 5a-c, preventive administration of curcumin was markedly more effective in inhibiting PDXs derived from EG2, EG37 and EG60 than giving curcumin only after innoculation of tumors. In these PDXs, curcumin inhibited STAT3 phosphorylation and the expression of STAT3-regulated Cox2 (Fig. 6e-h). Furthermore, TUNEL assay revealed that apoptosis in the tumor tissues were significantly increased by curcumin treatment (Fig. 6c and d). Taken together, our data indicated that curcumin inhibited JAK2 and blocked the activation of STAT3, leading to decreased expression of STAT3-regulated genes and increased apoptosis in ESCC cells and primary tumors. Therefore, the natural product might be used as an effective chemoprevent agent for ESCC.
STAT3 signaling is an important mechanism for the development of at least certain ESCC. In this study, we showed that curcumin may inhibit JAK2 and blocked STAT3 signaling pathway, resulting in growth inhibition and apoptosis of these ESCC cells. Therefore, STAT3 system appears to be an effective target in ESCC and curcumin is able to target the system to prevent and treat ESCC.
This work was supported by the National Natural Sciences Foundation of China (U1304813), the Science Foundation of the Henan Province of China (17A310032), Young Teacher Special Fund of Zhengzhou University (1421328055), Foundation and Frontier Technology Research Project in Henan Province (142300410325) and Natural Science Foundation of Jiangsu Province (BK20171231).
Availability of data and materials
All data generated or analyzed during this study are included in this published article.
YL, XW, SZ, XiaZ, JZ, XiaoZ, XC, WY, ZD, JZ and XX performed the experiments. YY, XX and FT wrote and edited the manuscript. XX and FT designed the research project. All authors read and approved the final manuscript.
Ethics approval and consent to participate
This study was approved by the Review Board and Ethical Committee of Zhengzhou University.
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
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