Discovery of a Novel Benzenesulfonamide Analogue That Inhibits Proliferation and Metastasis Against Ovarian Cancer OVCAR-8 Cells.

BACKGROUND: Ovarian cancer has been a salient public health concern in the world. It is necessary to develop novel antitumor drugs to treat ovarian cancer.
PURPOSE: This study investigated the synthesis, antiproliferation ability, antitumor mechanisms in vitro and in vivo of a novel benzenesulfonamide derivative.
METHODS: The novel benzenesulfonamide-1,2,3-triazole hybrid 7c was synthesized from 4-fluorobenzenesulfonyl chloride, prop-2-yn-1-amine and 1-(azidomethyl)-3-phenoxybenzene. The structure of this benzenesulfonamide-1,2,3-triazole hybrid 7c was confirmed by 13C NMR, and 1H NMR. Compound 7c was evaluated for its antitumor effects in vitro and in vivo against ovarian cancer OVCAR-8 cells.
RESULTS: We discovered that the benzenesulfonamide hybrid 7c potently inhibited cell proliferation against ovarian cancer. Especially, it inhibited cell proliferation with an IC50 value of 0.54μM against OVCAR-8 cells. It could inhibit migration and invasion against OVCAR-8 cells in a concentration-dependent and time-dependent manner. In addition, compound 7c affected the Wnt/β-catenin/GSK3β pathway against ovarian cancer OVCAR-8 cells. In vivo study suggested that compound 7c inhibited tumor growth remarkably without obvious toxicity.
CONCLUSION: In conclusion, benzenesulfonamide hybrid 7c could be a lead compound for further antitumor drug discovery to treat ovarian cancer.

Introduction

Ovarian cancer as a salient public health concern remains the deadliest form of gynaecological malignancy.1,2 According to the world health organization, an estimated total of 226,000 cases of ovarian cancer will be diagnosed and 140,200 patients will succumb to this disease every year in the world, representing the seventh most common form of cancer in women.3,4 Therefore, discovery of potent drugs against ovarian cancer is very necessary.

Benzenesulfonamide has become a biologically important object since its presence in the therapeutic application as the antitumor agent.5,6 Benzenesulfonamide derivative 1 (Figure 1) was known as a potent receptor tyrosine kinase inhibitor to treat renal cell carcinoma.7 Benzenesulfonamide derivative 2 was found to have a significant effect on the inhibition of antiapoptotic proteins Bcl2 and BclxL against HT-29 cells and SW620 cells.8 Benzenesulfonamide derivative 2 as a histone deacetylase inhibitor has been directed to treat peripheral T-cell lymphoma.9 In addition, 1,2,3-triazole-based heterocycles have been reported to possess the anticancer activity.10,11 1,2,3-Triazole 4 could arrest cell cycle at the G0/G1 phase in MCF-7 cells.12 1,2,3-Triazole 5 arrested the cell cycle in the G1/S phase and induced apoptosis against A549 cells.13 1,2,3-Triazole 6 exhibited the antiproliferative activity against acute myeloid leukemia cells by inhibiting histone deacetylases and tubulin acetylation.14 Based on these interesting findings, we hypothesised that the benzenesulfonamide-1,2,3-triazole hybrid may display the antiproliferative activity.

Figure 1

Anticancer benzenesulfonamide derivatives and 1,2,3-triazole derivatives.

In continuation of our effort to obtain the bioactive benzenesulfonamide derivative with potent antitumor abilities, we reported a novel benzenesulfonamide analogue containing the 1,2,3-triazole moiety, and furthermore examined its cytotoxic effect against ovarian cancer. We also revealed that this benzenesulfonamide-1,2,3-triazole hybrid as an antitumor agent could suppress OVCAR-8 cells proliferation, migration and invasion via Wnt/β-catenin/GSK3β pathway.

Materials and Methods

Synthesis of the Benzenesulfonamide Derivative

Reagents and solvents were purchased from commercial sources. 4-Fluorobenzenesulfonyl chloride (2 mmol) was reacted with prop-2-yn-1-amine (3 mmol) in the presence of sodium hydroxide (2.5 mmol) and dichloromethane (10 mL) to obtain the intermediate 7b without the further purification.15 Alkyne intermediate 7b (1 mmol), azide derivative (1 mmol), CuSO4.5H2O (0.2 mmol) and sodium ascorbate (0.1 mmol) were dissolved in acetone/H2O (4 mL/4 mL) and stirred for 10 hrs at room temperature. Upon completion of the reactions, the precipitated product 7c was purified with column chromatography on silica gel (hexane/EtOAc = 9/1). The chemical route and NMR data were shown in the .

Cell Culture

Cancer cell lines (MCF7, MGC803, EC109, HepG-2, PC-3, A549, OC-314, KYSE-450 and SK-N-SH) were purchased from GeneChem (Shanghai, China), cancer cell lines (OVCAR-8, SKOV3 and Caov-3) were purchased from Type Culture Collection of the Chinese Academy of Sciences (Shanghai, China). All cells were cultured in RPMI 1640 (Hyclone, Logan, UT, USA), supplemented with 10% foetal bovine serum (Hyclone, Logan, UT, USA) in a humidified CO2 (5%) incubator at 37°C.

Cell Viability Assay

1.0 × 105 cells per well were seeded in the 96-well plates. Following treatment with the compound, the cell viability was detected using the cell proliferation assay kit (Promega Corporation, Madison, WI) according to the manufacturer’s protocol. The absorbance at 570 nm was examined by a microplate reader to analysize the IC50 values.

Migration Assay

OVCAR-8 cell line was seeded and grown in a migration plate (Corning, USA). 20% FBS media or a vehicle was added in the upper bottom for 24 hrs. Fresh medium containing the compound was added to the plates. Images were taken using an inverted microscope (Nikon, Japan).

Invasion Assay

OVCAR cells were seeded in a transwell plate with the invasion membrane (LKT labs, USA). 20% FBS media or a vehicle was added in the upper bottom for 24 hrs. Fresh medium containing the compound was added for 48 hrs. Images were taken using an inverted microscope (Nikon, Japan).

Western Blotting Analysis

OVCAR cells were treated with the compound for 48 hrs. Proteins in the cell lysates were resolved by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, and then transferred to polyvinylidene fluoride membrane. Then, the membranes were incubated with the primary antibodies overnight at 4°C. The protein signals were visualized using the chemiluminescent substrate (KPL, Guildford, UK).

Xenograft Study

Animals were treated according to protocols established by the ethics committee of Zhengzhou University and the in vivo experiments were carried out in accordance with the approved guidelines and approved by the ethics committee of Zhengzhou University. Nude mice were maintained under specific pathogen-free conditions according to the Zhengzhou university committee protocol. OVCAR cells were subcutaneously injected into the right flanks of nude mice. Then, the mice were randomly assigned to the control group and the treatment group. The control group received the vehicle (0.9% NaCl) alone, and the treatment group received the compound for 21 days. The body weight and tumor size of each mouse was measured every other day. All data were analysized by GraphPad software.

Results and Discussion

Globally, ovarian cancer is the seventh most common cancer in women and the eighth most common cause of cancer death, with five-year survival rates below 45%.16 It is necessary to develop the potent anticancer against ovarian cancer. In addition, benzenesulfonamide and 1,2,3-triazole have been reported to possess the antitumor activity.5,17 In this investigation, we synthesized a novel benzenesulfonamide-1,2,3-triazole hybrid and explored its anticancer mechanisms against ovarian cancer.

Chemical Synthesis of the Benzenesulfonamide Hybrid 7c

The novel benzenesulfonamide-1,2,3-triazole hybrid 7c was synthesized in Scheme 1. 4-Fluorobenzenesulfonyl chloride 7a was reacted with prop-2-yn-1-amine in the presence of sodium hydroxide to obtain 7b without the purification.18,19 Compound 7c was readily synthesized from the crude product 7b and the 1-(azidomethyl)-3-phenoxybenzene via click reaction in the presence of copper(II) sulfate pentahydrate. The NMR data of this benzenesulfonamide-1,2,3-triazole hybrid 7c were shown in the .

Scheme 1

Reagents and conditions: (a) sodium hydroxide, prop-2-yn-1-amine, dichloromethane, rt.; (b) 1-(azidomethyl)-3-phenoxybenzene, sodium ascorbate, CuSO4.5H2O, acetone/H2O = 1:1.

Benzenesulfonamide Hybrid 7c Was a Potential Antiproliferative Agent Against Various Cancer Cell Lines

In order to investigate the antiproliferation ability of compound 7c, MCF7 cells (breast cancer cells), MGC803 (gastric cancer cells), EC109 (esophagus cancer cells), HepG-2 (liver cancer cells), PC-3 (prostate cancer cells), A549 (lung cancer cells), OC-314 (ovarian cancer cells), KYSE-450 (esophagus cancer cells), and SK-N-SH (neuroblastic cancer cells) were treated with compound 7c at different concentrations (control, 2μM, 4μM, and 8μM). From the results of Figure 2, compound 7c displayed the potential antiproliferative activity against all these cancer cell lines. Among them, compound 7c showed the most potent antiproliferation efficiency around 70% and 80% for 48 hrs and 72 hrs at 4μM concentration against ovarian cancer OC-314 cells.

Figure 2

Antiproliferative ability of compound 7c at different concentrations (control, 2μM, 4μM, and 8μM) for 48 hrs and 72 hrs against various cancer cell lines. The data were presented as the mean ± SEM. *P < 0.05, **P < 0.01.

Benzenesulfonamide Hybrid 7c Potently Inhibited Cell Proliferation Against Ovarian Cancer

Based on the preliminary experimental results, concentrations of 0.5μM, 1μM, 2μM, and 4μM were chosen to test the proliferation effects of compound 7c on the cell viability of ovarian cancer cells (OC-314, OVCAR-8, SKOV3, and Caov-3). We added the 5-Fluorouracil as a positive control to do the cytotoxicity assays in cancer cell lines (OC-314, OVCAR-8, SKOV3, and Caov-3). The IC50 values of 5-Fluorouracil against OC-314, OVCAR-8, SKOV3, and Caov-3 cells were 3.12μM, 2.24μM, 22.5μM and 10.7μM, respectively. As shown in Figure 3, OVCAR-8 cells displayed a marked loss in cell viability following the treatment at 2μM and 4μM for 48 hrs. From the results of Figure 3, compound 7c inhibited cell proliferation with IC50 values of 1.82μM, 0.54μM, 3.91μM, and 2.13μM against OC-314, OVCAR-8, SKOV3, and Caov-3 cell lines. These findings supported that the benzenesulfonamide hybrid 7c potently inhibited cell proliferation against ovarian cancer in a concentration-dependent manner.

Figure 3

Benzenesulfonamide 7c potently inhibited cell proliferation against ovarian cancer cell lines (OC-314, OVCAR-8, SKOV3, and Caov-3) in a concentration-dependent manner. The data were presented as the mean ± SEM. **P < 0.01, ***P < 0.001.

Benzenesulfonamide Hybrid 7c Inhibited Migration Against Ovarian Cancer OVCAR-8 Cells

To investigate the effects of benzenesulfonamide hybrid 7c in endothelial cell migration against ovarian cancer OVCAR-8 cells, the migration assay was explored according to the previous reference.20 As shown in Figure 4A and C, the migration rates with the treatment of 7c for 48 hrs at 0.25μM, 0.5μM and 1μM were 62.4%, 37.5% and 7.3%, respectively. From the migration results of Figure 4B and D, the migration rates with the treatment of 7c at 0.25μM for 24 hrs, 48 hrs and 72 hrs were 73.3%, 61.4%, and 20.8%, respectively. All these illustrated that benzenesulfonamide-1,2,3-triazole hybrid 7c could inhibit OVCAR-8 cells migration in a concentration-dependent manner.

Figure 4

(A and C): OVCAR-8 cells were treated with 7c for 48 hrs at 0.25μM, 0.5μM and 1μM to evaluate the migration rates. (B and D): OVCAR-8 cells were treated with 7c at 0.25μM for 24 hrs, 48 hrs and 72 hrs to evaluate the migration rates. **P < 0.01 and ***P < 0.001 were considered statistically significant compared with the control.

Benzenesulfonamide Hybrid 7c Could Suppress OVCAR-8 Cells Invasion

In addition, the invasion ability of benzenesulfonamide-1,2,3-triazole hybrid 7c against OVCAR-8 cells was also evaluated by matrigel-coated transwell. Based on the invasion results of Figure 5A and C, the invasion rates with the treatment of 7c for 48 hrs at 0.25μM, 0.5μM and 1μM were 76.1%, 60.2% and 20.3%, respectively. When OVCAR-8 cells were treated with 7c at 0.5μM, the invasion rates for 24 hrs, 48 hrs and 72 hrs were 60.6%, 30.4%, and 9.1%, respectively. The matrigel offered a simulant biologicalstroma, and ovarian cancer OVCAR-8 cells were blocked to invade by the benzenesulfonamide hybrid 7c in a concentration-dependent and time-dependent manner.

Figure 5

(A and C): OVCAR-8 cells were treated with 7c for 48 hrs at 0.25μM, 0.5μM and 1μM to evaluate the invasion effects. (B and D): OVCAR-8 cells were treated with 7c at 0.5μM for 24 hrs, 48 hrs and 72 hrs to evaluate the invasion effects. **P < 0.01 and *P < 0.05 were considered statistically significant compared with the control.

Benzenesulfonamide Hybrid 7c Affected the Epithelial-Mesenchymal Transition Related Markers

The phenomenon that epithelial cells acquire mesenchymal traits, termed as epithelial-mesenchymal transition (EMT), has been observed in physiological and pathological processes, including cancer progression.21 Loss of E-cadherin and increase of N-cadherin expression levels were considered key events in an EMT process where the cell polarity-related cytoskeleton, cell-cell contacting modulators and extracellular matrix were involved.22 Based on the migration and invasion effects of benzenesulfonamide-1,2,3-triazole hybrid 7c against OVCAR-8 cells, the expression levels of EMT related markers (E-cadherin, N-cadherin and Snail-1) were evaluated by Western blot methods. As shown in Figure 6, benzenesulfonamide-1,2,3-triazole hybrid 7c could decrease the expression levels of N-cadherin and Snail-1, and increase the expression level of E-cadherin in a concentration-dependent manner.

Figure 6

OVCAR-8 cells were treated with 7c for 48 hrs at 0.25μM, 0.5μM and 1μM to test the expression levels of EMT related markers (E-cadherin, N-cadherin, and Snail-1). **P < 0.01 and *P < 0.05 were considered statistically significant compared with the control.

Benzenesulfonamide Hybrid 7c Affected the Wnt/β-Catenin/GSK3β Pathway Against Ovarian Cancer OVCAR-8 Cells

Wnt/β-catenin is a conserved cell-signaling system that is involved numerous biological processes such as organogenesis in multicellular organisms cancer pathogenesis and the epithelial-mesenchymal transition (EMT) process.23 Some 1,2,3-triazoles recently described as inhibitors of the wnt/β-catenin signaling pathway.24 In addition, celecoxib as a sulfonamide selective COX-2 inhibitor inhibited human colon cancer cell proliferation by suppressing the Wnt/β-catenin signaling pathway.25 Because of the same 1,2,3-triazole scaffold in the hybrid 7c, we also explored its effects on the wnt/β-catenin signaling pathway. Glycogen synthase kinase-3β (GSK3β) as a serine/threonine protein kinase has been implicated in a wide range of diseases including cancer.26 The inhibition of GSK-3β could lead to β-catenin activation and tumor cell proliferation.27 There is increasing evidence to show that GSK3β was aberrantly activated in various cancer types and related to tumor invasion.28 To further investigate whether compound 7c inhibited OVCAR-8 cells migration and invasion via a wnt/β-catenin signaling pathway, seven wnt/β-catenin pathway-related proteins of Wnt 3a, β-catenin, GSK3β, C-Myc, Cyclin-D, Axin2 and TCF4 were tested in OVCAR-8 cells and examined by Western blot analysis. Western blot analysis showed that the expression level of GSK3β was significantly enhanced after treatment of OVCAR-8 cells with compound 7c compared with the control group (Figure 7). The results exhibited that proteins Wnt 3a, β-catenin, C-Myc, Cyclin-D, Axin2, and TCF4 were significantly downregulated after 48 hrs treatment.

Figure 7

OVCAR-8 cells were treated with 7c for 48 hrs at 0.25μM, 0.5μM and 1μM to explore the expression levels (Wnt 3a, β-catenin, GSK3β, C-Myc, Cyclin-D, Axin2 and TCF4). **P < 0.01 and ****P < 0.0001 were considered statistically significant compared with the control.

In vivo Antitumor Study of Benzenesulfonamide Hybrid 7c

To elucidate the antitumor effects of benzenesulfonamide-1,2,3-triazole hybrid 7c in vivo, OVCAR-8 xenograft models were used. Tumor-bearing mice were then randomly assigned to two groups (control and 100 mg/kg 7c) with 5 mice per group. The treatment group received intragastric administration of 7c per day for a period of 21 days. The results showed that benzenesulfonamide 7c suppressed OVCAR-8 subcutaneous tumor growth (Figure 8). The average tumor weights of control and benzenesulfonamide-1,2,3-triazole hybrid 7c groups were 1.23 ± 0.30 g and 0.47 ± 0.20 g (inhibitory rate: 61.79%), respectively. The relative tumor volume in the benzenesulfonamide 7c group (100 mg/kg) was reduced. Benzenesulfonamide 7c treatment did not significantly decrease the mouse body weight compared with that of the control. As shown in Figure 8, compound 7c inhibited tumor growth remarkably, suggesting its antitumor efficacy.

Figure 8

In vivo antitumor effects of compound 7c. (A): Tumor volume. (B): Tumor weight. (C): Body weight. (D): Representative tumor size after treatment with compound 7c. **P < 0.01 were considered statistically significant compared with the controls.

Conclusion

In this work, we synthesized a novel benzenesulfonamide-1,2,3-triazole hybrid, and furthermore examined its cytotoxic effect against nine cancer cell lines (MCF7, MGC803, EC109, HepG-2, PC-3, A549, OC-314, KYSE-450, and SK-N-SH). Among them, compound 7c showed the most potent antiproliferation effects against ovarian cancer OC-314 cells with percentages of 32.3% and 20.7% for 48 hrs and 72 hrs at 4μM concentration. In addition, compound 7c inhibited cell proliferation with IC50 values of 1.82μM, 0.54μM, 3.91μM, and 2.13μM against OC-314, OVCAR-8, SKOV3, and Caov-3 cell lines, investigating that compound 7c displayed the potent antiproliferation effects against ovarian cancer.

Furthermore, benzenesulfonamide-1,2,3-triazole hybrid 7c potently inhibited migration and invasion against ovarian cancer OVCAR-8 cells in a concentration-dependent and time-dependent manner. It could decrease the expression levels of Wnt 3a, β-catenin, C-Myc, Cyclin-D, Axin2, TCF4, N-cadherin and Snail-1, and increase the expression levels of E-cadherin and GSK3β. All these results revealed that compound 7c affected the Wnt/β-catenin/GSK3β pathway against ovarian cancer OVCAR-8 cells. Importantly, compound 7c inhibited tumor growth remarkably, while the body weight was almost unchanged, suggesting the antitumor efficacy and low global toxicity. Collectively, we identify that compound 7c could be a lead compound for further antitumor drug discovery to treat ovarian cancer.