A correction has been applied to this article in:
Corrigendum: Terminalia catappa leaf extracts inhibited metastasis of A2058 and A375 melanoma cells via downregulating p-Src and β-catenin pathway in vitro
Chin-Kuo Chang
Shu-Chen Chu
Jing-Yang Huang1,3
Pei-Ni Chen- 1Institute of Medicine, Chung Shan Medical University, Taichung, Taiwan
- 2Institute and Department of Food Science, Central Taiwan University of Science and Technology, Taichung, Taiwan
- 3Department of Medical Research, Chung Shan Medical University Hospital, Taichung, Taiwan
- 4Department of Biochemistry, School of Medicine, Chung Shan Medical University, Taichung, Taiwan
- 5Clinical Laboratory, Chung Shan Medical University Hospital, Taichung, Taiwan
Background: Melanoma is a highly aggressive, lethal, and malignant cancer. Once diagnosed early, it can be easily removed and cured with satisfaction. Although many methods such as surgery, chemotherapy, radiotherapy, and immunotherapy have been used to treat this disease at an advanced stage, the outcomes are poor. Terminalia catappa leaves have been shown to have various biological benefits, including antitumor activity. The specific effects and molecular mechanisms of Terminalia catappa leaf in treating A2058 and A375 melanoma cells in vitro need to be clarified.
Methods: The A2058 and A375 melanoma cancer cells were treated with Terminalia catappa leaf extracts, and then the effect of Terminalia catappa leaf extracts on migration and invasion was examined. The cell migration/invasion capacities of A2058 and A375 cells were investigated by a modified Boyden chamber assay. Zymography was used to clarify the activities of matrix metalloproteinases-2 and urinary type plasminogen activator. We performed a Western blot to verify the related expression of phospho-Src (Tyr416), phospho-Focal adhesion kinase (Tyr397), Vimentin, and β-catenin.
Results: Modified Boyden chamber assays demonstrated that treatment of Terminalia catappa leaf extracts significantly inhibited A2058 and A375 cell migration/invasion capacities. In the zymography results, we showed that Terminalia catappa leaf extracts negatively modulated the activities of matrix metalloproteinases-2 and urinary type plasminogen activator. Western blot indicated that Terminalia catappa leaf extracts reduced the expression of phospho-Src (Tyr416), phospho-Focal adhesion kinase (Tyr397), Vimentin, and β-catenin.
Conclusion: Terminalia catappa leaf extracts affected the antimetastasis of the A2058 and A375 melanoma cell lines by inhibiting the Focal adhesion kinase/Src interaction and Wingless-int1/β-catenin pathways in vitro. Terminalia catappa leaf extracts may serve as an effective chemopreventive agent against metastasis of melanoma cancer.
1 Introduction
Melanoma is a highly aggressive and deadly form of skin cancer caused by various risk factors, including environmental or genetic causes such as UV exposure and sunlight (Lo and Fisher, 2014). Melanoma with increasing incidence and mortality rate has been found in recent decades (Volkovova et al., 2012). Resistance to chemotherapy, radiation therapy and immunotherapy often results in ineffective treatment of the metastatic melanoma. Metastatic melanoma patients with a 5-year survival rate only occupied less than 20% (Sandru et al., 2014). Surgery can cure localized melanoma early, but treatment is ineffective for metastatic melanoma (Yilmaz and Christofori, 2009; Simoes et al., 2015).
During epithelial-mesenchymal transition (EMT), cancer cells aggressively infiltrate the blood vessels and lymphatic system and transfer to other organs or tissues, forming a metastatic tumor. In the process of EMT, inhibition of E-cadherin and promotion of Vimentin, N-cadherin, Focal adhesion kinase (FAK), Src, Snail, and Twist in cell junctions can be initiated at the molecular level (Lamouille et al., 2014). Changes in surface adhesion properties, cell migration and invasion, penetration into vascular or lymphoid tissues, degradation of the extracellular matrix (ECM), and infiltration into nearby tissues are among the various events triggered during cancer metastasis (Westermarck and Kahari, 1999; Gupta and Massague, 2006).
Degradation of components in the basement membrane and extracellular matrix occurs during metastasis, resulting from the combined action of multiple proteases, such as plasminogen activator (PA), matrix (MMPs), cathepsins, in tumor metastasis and plays a crucial role in the invasion transfer process (Westermarck and Kahari, 1999). The expression of matrix metalloproteinases-2 (MMP-2) has been reported to correlate with various tumors (Stetler-Stevenson, 1999). In addition to MMP, the serine protease urinary type plasminogen activator (u-PA) converts inactive plasminogen to active plasmin and elicits a cascade of the proteolytic process to degrade the extracellular matrix (Baricos et al., 1995). Enhanced activity and expression of MMP-2 have a significant impact on survival and outcomes in human malignancies (Stearns and Stearns, 1996; Talvensaari-Mattila et al., 1998; Kallakury et al., 2001; Yoshizaki et al., 2001). u-PA is present in cellular structures on the leading edge of migrating cells and regulates cell adhesion, migration, invasion, and metastasis (Duffy and Duggan, 2004). Therefore, MMP or u-PA has a controlling effect on cancer metastasis, which will be considered as a feasible method. (Bjorklund and Koivunen, 2005). FAK is overexpressed and hyperphosphorylated in multiple cancer cells, and recent reports have elucidated that this kinase is responsible for cell migration (Fan et al., 2016), survival (Skinner et al., 2016), proliferation (Balsas et al., 2017), and adhesion (Nader et al., 2016). Focal contacts are built at the ECM integration junctions that bring together the cytoskeleton and signaling proteins during cell adhesion, spread, and migration (Maziveyi and Alahari, 2017).
FAK activity can be initiated by ECM or growth factors. Previous studies have found that tyrosine phosphorylation regulates focal contact assembly and can occur rapidly (Parsons, 2003). Using the FAK mutation at Tyr397, a binding site for Src, the study verified that while downregulating cell migration, this mutation releases a pool of active Src that modulates enhanced invadopodia activity (Mousson et al., 2021). Inhibition of the FAK/Src interaction enhances the proteolytic activity of invasive melanoma cells (Mousson et al., 2021). Importantly, Src plays a control role in the expression of E-cadherin (Serrels et al., 2011). In breast cancer cells, inhibition of Src induces a reverted epithelial phenotype associated with an increase in E-cadherin and a decrease of Vimentin, and it blocks cancer cell migration (Liu and Feng, 2010). The oncogenic expression of Src in pancreatic tumor cells was also associated with a reduced expression of E-cadherin in favor of Vimentin (Nagathihalli and Merchant, 2012).
The importance of canonical Wingless-int1 (Wnt) signaling in melanoma initiation is associated chiefly with β-catenin ability to regulate the expression of a wide range of genes of the melanocyte lineage, and its involvement in the regulation of proliferation is probably related to the activation of microphthalmia-associated transcription factor (MITF) expression (Widlund et al., 2002; Larue and Delmas, 2006; Levy et al., 2006; Hoek et al., 2008; Arozarena et al., 2011; Kawakami and Fisher, 2017). β-catenin mediates the transcriptional expression of Wnt target genes (Tarapore et al., 2012; Uzdensky et al., 2013; Kahn, 2014). While the Wnt pathway activation is “turn on”, β-catenin enters the nucleus and engages DNA-bound TCF transcription factors (Behrens et al., 1996) (Molenaar et al., 1996). Numerous studies demonstrated that aberrant activation of Wnt-signaling contributed to malignant cell transformation and neoplastic proliferation with further metastatic dissemination and resistance to treatment (Ring et al., 2014; Galluzzi et al., 2019). In several studies of hepatocellular carcinoma, melanoma, and acute myeloid leukemia, FAK operated upstream of Wnt, while in prostate cancer, Wnt appeared to act upstream of FAK. Furthermore, a study of renal carcinoma revealed that Wnt and FAK might work simultaneously in promoting cancer progression (Worthmuller and Ruegg, 2020). The depletion of FAK in hepatocytes blocked tumor proliferation and prolonged survival in a c-Met/β-catenin-driven hepatocellular carcinoma (HCC) mouse model (Shang et al., 2015), suggesting that FAK is required for c-Met/β-catenin-driven hepatocarcinogenesis. Another study showed that FAK and β-catenin synergistically induced HCC in mice (Shang et al., 2019) and that FAK elicited Wnt/β-catenin signaling, activated cancer stem cell (CSC) traits, and initiated tumorigenicity in HCC cells (Fan et al., 2019).
The Terminalia catappa leaf is biologically active, including antioxidants (punicalagin, punicalin, chebulic acidcoumaric acid, benzoic acid, terfluvina A and B, and their derivatives) (Chen and Li, 2006; Kinoshita et al., 2007), antidiabetic (beta - carotene) (Anand et al., 2015), anticancer (punicalagin) (Naitik et al., 2012), antiviral (ellagic acid) (Tan et al., 1991), anti-inflammatory (triterpene acids, especially ursolic acid and its derivatives) (Fan et al., 2004), antibacterial (flavonoids and flavanols) (Kloucek et al., 2005; Shinde et al., 2009), and hepatoprotective activity (punicalagin, punicalin) (Kinoshita et al., 2007). Terminalia catappa leaf extracts (TCE) effectively inhibits phosphorylation of the ERK1/2 signaling pathway by negatively regulating the activity of the DNA binding factor SP-1 and NF-κB DNA-binding activity, thereby inhibiting u-PA and inhibiting metastasis (Yeh et al., 2014). TCE had an antitumor influence in Ehrlich ascites carcinoma (EAC)-bearing mice with EAC (Pandya et al., 2013) by modulating Lipid Hydroperoxide (LPO) and reinforcing the antioxidant defense system. In this report, our goal was to study the efficacy of TCE on antimetastasis of the A2058 and A375 melanoma cell line and related mechanisms that will contribute to humans.
2 Materials and methods
2.1 Preparation of TCE
Terminalia catappa leaves were obtained from a traditional herbal medicine store in Taichung. Terminalia catappa ethanol extracts were prepared by initial condensation and lyophilization as previously described (Chu et al., 2007). Briefly, 100 g of air-dried leaves were boiled at 70°C with 500 ml of 50% ethanol for 24 h. We removed the solvent by using a vacuum rotary evaporator. These fractions were then lyophilized and stored at −20°C. Next, we dissolved the TCE powder in 50% dimethyl sulfoxide (DMSO) to achieve an indicated concentration with the highest DMSO concentration of less than 0.1%.
2.2 Cell and cell culture
We obtained A2058 and A375 human melanoma cell lines from the Bioresource Collection and Research Center (BCRC, Hsinchu, Taiwan) and cultured them in Dulbecco’s Modified Eagle Medium (DMEM). All cell cultures were kept in a humidified atmosphere at 37°C containing 5% CO2.
2.3 Determination of cell viability (MTT assay)
TCE cytotoxicity was evaluated using an MTT colorimetric assay (Sigma) (Mosmann, 1983; Yang et al., 2008) to analyze cell viability. After seeding in 24-well plates at a density of 5 × 104 cells/well, A2058 cells, A375 and Hs68 cells were treated with TCE, respectively, at a concentration between 0 and 100 μg/ml at 37°C for 24 h. The medium was removed after 24 h of incubation, and the two cells were washed with phosphate-buffered saline (PBS) 3 times and then incubated with 20 μL of MTT (5 mg/ml) (Sigma Chemical Co., St. Louis, MO, United States) for 4 h. The number of viable cells per plate was measured spectrophotometrically at 563 nm after solubilization with isopropanol.
2.4 Determination of urinary type plasminogen activator and matrix metalloproteinase 2 by zymography
MMP-2 in a conditioned medium were examined using gelatin zymography protease assays, as previously described (Chu et al., 2007). To prepare samples, we used a standard sodium dodecyl sulfate gel loading buffer containing 0.01% SDS without β-mercaptoethanol without boiling or reduction. The collected samples were then subjected to 8% sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) (0.75-mm; acrylamide/bis-acrylamide 30/1.2; containing 0.1% gelatin; Sigma). Electrophoresis was performed for 3 h at 140 V in an OWL P-1 apparatus (Alpha Multiservices, Inc., Contoe, TX, United States). After electrophoresis, we used 100 ml of distilled water containing 2% Triton X100 (Sigma) to wash the gels twice. The gels were then incubated in reaction buffer (40 mM Tris-HCl, pH 8.0, 10 mM CaCl2, 0.02% NaN3; Sigma) at 37°C for 12 h, stained with Coomassie brilliant blue R250 and destained with methanol/acetic acid/water (50/75/875, v/v/v; Sigma). The activity of u-PA was verified as previously described (Chu et al., 2007). 2% w/v casein and 20 μg/ml plasminogen (Sigma) were added to 8% SDS-PAGE gels. Electrophoresis and zymography were performed for gelatin zymography.
2.5 Wound healing migration assay
We used silicon culture inserts (Ibidi, Munchen, Germany) with two individual wells. For cell seeding, a wound closure seeding model was managed to determine whether TCE could suppress A2058 cell migration and A375 cell migration, respectively. Each insert was placed in a culture plate, and A2058 or A375 were seeded with 1.5 × 104 cells/well and grown to form a confluent and homogeneous layer. After incubation for 24 h, the culture insert was removed, and the wound zone could be found. The medium was removed and replaced with DMEM containing 1% FBS, and then TCE was added. We incubated the two cells at 37°C and photographed the movement of the cells in the wound zone at 0 h, 24 h, and 48 h using a phase-contrast microscope (×40).
2.6 Cell invasion and migration assays
To validate the motility and invasion, a Boyden chamber assay (Neuro Probe, Cabin John, MD, United States) with a pore size of 8 μm for the migration assay and a matrix barrier of 10 μg/ml Matrigel (BD Biosciences, MA, United States) for the invasion assay, respectively. First, we treated A2058 and A375 cells with TCE at different concentrations (0, 25, 50, and 100 μg/ml) for 24 h. The surviving cells and seeded in a Boyden chamber with 1.5 × 104 cells/well in a serum-free medium and incubated at 37°C for 12 h. For the invasion assay, 10 μg/ml Matrigel® (25 mg/50 ml; BD Biosciences, Bedford, MA, United States) was applied to 8-μm-pore-size polycarbonate membrane filters (Neuro Probe, Cabin John, MD, United States), and the bottom chamber was contained with a traditional medium. Following incubation, the filters were air-dried for 5 h in a laminar flow hood. We fixed invading cells with methanol and stained them with Giemsa (Sigma). We counted cell numbers with a light microscope (CKX41; Olympus), and the migration assay was practiced as described for the Matrigel invasion assay, without the coating (Chen et al., 2006).
2.7 Preparation of total cell lysates
For the preparation of total cell lysates, cells were rinsed twice with PBS and scraped with 0.2 ml of cold RIPA buffer containing protease inhibitor cocktail, then vortexed at 4°C for 10 min. Cell lysates were subjected to 13,000 rpm centrifugation for 10 min at 4°C, and the insoluble pellet was discarded. Briefly, harvested cells were scraped and lysed with buffer A (10 mM HEPES, 10 mM KC1, 0.1 mM EDTA, 1.5 mM MgCl2, 0.2% NP40, 1 mM DTT, and 0.5 mM phenylmethylsulfonylfluoride), followed by vortexing to shear the cytoplasmic membranes were collected by centrifugation at 13,000 rpm for 30 s at 4°C. Finally, we performed a Bradford assay (Bradford, 1976) to verify the concentration of total cell lysates.
2.8 Western blot analysis
A 6 cm dish with seeded cells was incubated for 24 h. TCE was added with an indicated concentration (0, 25, 50, and 100 μg/ml) for 24 h. We used the PRO-PREP protein extraction solution (iNtRON), containing the protease inhibitor, to collect total cell lysates. Subsequently, the cell extracts were microcentrifuged at 13,000 rpm for 30 min at 4°C, and the supernatants were obtained. Cell lysates were separated on a 10% polyacrylamide gel and transferred to a nitrocellulose membrane. And the blot was incubated with 5% non-fat milk in PBS for 1 h to block non-specific binding and then the corresponding antibodies overnight against GAPDH (Santa Cruz Biotechnology Inc., Santa Cruz, CA), Vimentin (Santa Cruz Biotechnology Inc., Santa Cruz, CA), p-Src (Tyr416) (Cell Singling Technology, Inc., Danvers, MA, United States), t-Src (Cell Singling Technology, Inc., Danvers, MA, United States), p-FAK (Tyr397) (Cell Singling Technology, Inc., Danvers, MA, United States), t-FAK (Cell Singling Technology, Inc., Danvers, MA, United States) and β-catenin (Gene Tex. Inc. Irvine, CA, United States). The cells were then incubated at 37°C with an appropriate peroxidase-conjugated secondary antibody for 1 h. Then we used enhanced chemiluminescence (ECL) commercial kit (Amersham Biosciences) to obtain signals and quantitated the relative photographic density by scanning the photographic negatives on a gel documentation and analysis system (AlphaImager 2000; Alpha Innotech Corporation, San Leandro, CA, United States) (Yang et al., 2008).
2.9 Statistical analysis
Data are indicated as mean ± SD, and each experiment was performed in triplicate. Statistical significances were analyzed by two-way analysis of variance (ANOVA) with post hoc Tukey’s test.
The p-value <0.05 was indicated as statistically significant.
3 Results
3.1 The influence of TCE on the viability of A2058, A375 and Hs60 cells
The cytotoxic effects of TCE at various concentrations (0–100 μg/ml) on A2058 cells and A375 cells are shown in Figures 1A,B. The assay showed that even at the highest concentration of 100 μg/ml. TCE did not alter the viability of A2058 and had a little impact on A375 cells compared to controls. In addition, the effect of TCE on the cell viability of normal Hs60 fibroblasts was also investigated. As shown in Figure 1C, TCE did not alter the viability of Hs60 cells.
FIGURE 1
FIGURE 1. The effects of TCE cell viability. (A) A2058, (B) A375 cells and (C) normal dermal fibroblastHs68 were treatedwith TCE (0, 25, 50, 100 μg/ml), respectively, for 24 h by MTT assay. The values represent the means ± SD of at least three independent experiments. Comparisons were performed using two-way ANOVA with post hoc Turkey’s test (***p < 0.05).
3.2 Reduced effect of TCE on the activity of MMP-2
As shown in Figures 2A,B, TCE treatment in A2058 and A375 cells for 24 h and 48 h can reduce the activity of the MMP-2 protein, and this reduction was dose-dependent.
FIGURE 2
FIGURE 2. Effects of TCE on the activity of MMP-2. A2058 cells and A375 were treated with (0, 25, 50, 100 μg/ml) of TCE for 24 h and 48 h, respectively, then subjected to gelatin and casein zymography to analyze the activities of MMP-2 (A, B). The values represented the means ± SD of at least three independent experiments. Comparisons were performed using two-way ANOVA with post hoc Turkey’s test (***p < 0.05).
3.3 Reduced effect of TCE on the activities of u-PA
Figures 3A,B showed that TCE treatment in A2058 and A375 cells for 24 h and 48 h can suppress the activity of the u-PA protein, and this suppression was dose-dependent.
FIGURE 3
FIGURE 3. Effects of TCE on the activity of u-PA. A2058 cells and A375 were treated with (0, 25, 50, 100 μg/ml) of TCE for 24 h and 48 h, respectively, then subjected to gelatin and casein zymography to analyze the activities of u-PA (A, B). The values represented the means ± SD of at least three independent experiments. Comparisons were performed using two-way ANOVA with post hoc Turkey’s test (***p < 0.05).
3.4 Inhibitory effect on the motility of A2058 and A375 cells by TCE
Regarding the cell migration, we observed that after 24 h at concentration 0 μg/ml, 25 μg/ml, 50 μg/ml with TCE, the A2058 cells migrated and covered approximately 15%–35% of the wound area quantified in time zero for all abutment discs, the A375 cells 2%–13%. And after 48 h at concentration 0 μg/ml, 25 μg/ml, 50 μg/ml with TCE, the A2058 cells migrated and covered approximately 21%–97% of the wound area quantified in time zero for all abutment discs, the A375 cells 1%–32%. Lower migration was observed on A375 when compared to A2058. Initial wound edges marked initial cell migration and were used to identify the decrease in wound width throughout the experiment. Migration distances were showed separately during periods 0–24 h (migration during first 24 h period) and 0–48 h (during second 24 h period). On the two images recording period after wounding (0–24 h) (0–48 h) at 0 μg/ml, 25 μg/ml, 50 μg/ml 100 μg/ml with TCE, significant differences migration distance were found for A2058 discs when compared to the control (Figure 4A, ***p < 0.05), whilst no difference in motility was found on A375 discs after wounding (0–24 h) at 25 μg/ml concentration with TCE (Figure 4B, ***p < 0.05). Experiments are showed in triplicates (mean ± SD, ***p < 0.05).
FIGURE 4
FIGURE 4. The effects of TCE on the cell migration of A2058 and A375 cells. (A,B) Photographs showed wound closure of A2058 and A375 cells treated with TCE (0, 25, 50, 100 μg/mL) and 0, 24, 48 h. Cell wound healing assay was performed as described in the Materials and Methods. % Wound coverage was determined by the rate of cells moving forward the scratched area upon time. The values of percentagewound closure ± SD of at least three independent experiments. Comparisons were performed using two-way ANOVA with post hoc Turkey's test (***p < 0.05).
3.5 Inhibitory effect on migration and invasion of A2058 and A375 cells by TCE
It demonstrated that TCE significantly suppressed the invasion of A2058 and A375 cells in a concentration-dependent manner, only 38% and 20% remained after treatment of 100 μg/ml with TCE, respectively (Figures 5A,C), 38% and 22% left after cell migration (Figures 5B,D).
FIGURE 5
FIGURE 5. Effects of TCE on cell invasion and migration of A2058 and A375 cells. After being treated with TCE at a concentration of (0, 25, 50, 100 μg/mL) for 24 h, cell invasion and migration assay were then performed as described in the Materials and Methods. Representative images of A2058 and A375 cells on the lower side of membrane at different time points in the (A,C) invasion and (B,D) migration assay. A representative number of invading cells through the Matrigel and membrane were counted under the microscope for 10 random fields at a 3,200 magnification. The results were statistically evaluated using two-way ANOVA with post hoc Turkey's test (***p < 0.05). The results from 3 repeated and separate experiments were similar.
3.6 Down-regulated effect of the vimentin, p-FAK (Tyr397), p-Src (Tyr416), and β-catenin pathways by TCE
Since the inhibitory effect of TCE on cell migration/invasion and proteinases has been revealed, the effects of TCE on the β-catenin pathways were investigated by Western blot to clarify the underlying mechanisms. The Western blot results indicated that TCE could reduce the phosphorylation of β-catenin and p-Src (Tyr416) (Figures 6A,B) in A2058 and A375 cells. Additionally, TCE could also inhibit the expressions of Vimentin and p-FAK (Tyr397) in A2058 cells (Figure 6C).
FIGURE 6
FIGURE 6. A2058 and A375 cell lines were pretreated with TCE and then incubated for 24 h. The cells lysates were subjected to SDS-PAGE followed by western blotswith anti-β-catenin, anti-p-Src (Tyr416), anti-t-Src, anti-GAPDH (A, B) and anti-Vimentin, anti-p-FAK (Tyr397), anti-t-FAK, anti-GAPDH for A2058 (C), as described in Methods Section 2.8. The bar graph shows the statistical results of protein expression (D–F). The values represented the means ± SD of at least three independent experiments. Comparisons were performed using two-way ANOVA with post hoc Turkey’s test (***p < 0.05).
4 Discussions
In the past, our laboratory has also studied TCE in other cancer metastases (Chu et al., 2007; Yang et al., 2010; Yeh et al., 2012; Chung et al., 2021). We demonstrated that TCE negatively affected metastasis in various cancers, including hepatocellular carcinoma, oral cancer, human glioblastoma, and lung cancer. To explore in-depth the effect and mechanism of TCE in anticancer metastasis, we used various verification methods to analyze the actual biological results of TCE on the antimetastasis of melanoma in vitro. First, we found that TCE could reduce the expression of MMP-2 and u-PA, respectively, for 24 and 48 h in the zymography assay (Figure 2 and Figure 3). As we know, MMP-2, and u-PA pose an essential role during metastasis. Effective down-regulation of the function of MMP-2 and u-PA by TCE led to the depletion of ECM (Baricos et al., 1995). It showed that the down-regulated expression of MMP-2 lost its fundamental ability to facilitate metastasis activity under the effect of TCE. In the movement wound healing assay, TCE significantly hindered the moving ability of the A2058 and A375 cell lines at a concentration of 50 μg/ml and 100 μg/ml with TCE (Figure 4). Whether TCE could suppress the invasion and migration of A2058 and A375 melanoma cell lines, which we expected to elucidate, should be further addressed. In the invasion and migration assay, we verified that the A2058 and A375 cell lines were suppressed and unable to invade and migrate successfully (Figure 5).
In metastasis, u-PA could convert plasminogen to plasmin, eliciting MMP-2 to degrade ECM (Chen et al., 2011). u-PA interacted with integrin-β1 and then mediated FAK to increase the downstream cascade of the metastatic mechanism. Inhibited expression of u-PA decreased the degradation activity of ECM and consequently obstructed the signaling pathway of metastasis. FAK in cells plays a pivotal role in assembling various proteins to respond further once the metastatic mechanism is initiated (Sulzmaier et al., 2014). The FAK-Src complexes phosphates Paxillin Tyr118, facilitating the combination of ERK2 and paxillin. Excellular regulated protein kinases 2 (ERK2) phosphating paxillin triggers FAK combining with paxillin and activates FAK. FAK Tyr925 was phosphated by Src and influenced the generation of paxillin and vinculin complexes (Mitra and Schlaepfer, 2006). Furthermore, Rho/Rac/Cdc42 or MAPK, which mediates cell migration and morphology, can be enhanced by interacting upstream signaling pathways between FAK Tyr925 and Src. In Western blot, we discovered that p-Src was inhibited in our study. The β-catenin pathway was also negatively regulated. After TCE treatment, the Src and β-catenin signaling pathways were hindered in the A2058 and A375 melanoma cell lines (Figure 5). TCE had the effect of tempering the FAK/Src interaction and β-catenin signaling pathway from the investigation of Vimentin, p-FAK (Tyr397) and p-Src (Tyr416), and β-catenin which were negatively regulated in Western blot (Figure 6).
The expression of p-FAK (Tyr397) and p-Src (Tyr416) protein was suppressed in Western blot (Figure 6). Previous studies showed that melanoma cells might be hindered in accelerating invadopodia activity, and subsequently, Vimentin was suppressed (Liu and Feng, 2010; Nagathihalli and Merchant, 2012; Mousson et al., 2021). Involvement in regulating melanocyte proliferation, β-catenin is most likely associated with the activation of MITF expression (Larue and Delmas, 2006). Wnt and FAK might simultaneously encourage renal carcinoma progression in a previous study (Shang et al., 2015). Interestingly, we found that TCE inhibited the expression of FAK and β-catenin in our research. It may suggest that TCE could influence the effect of metastasis of A2058 and A375 melanoma cell lines.
In conclusion, our study raveled about the possibility of adjuvant treatment of melanoma in the future. Our study demonstrated that TCE had an effect on antimetastasis in the A2058 and A375 melanoma cell line in vitro.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Author contributions
C-KC contributed to the writing and submission. All authors contributed to the article and approved the publication.
Acknowledgments
The authors thank Y-SH, P-NC, and S-CC for providing many helpful expert opinions on this research.
Conflict of interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.
Supplementary material
The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2022.963589/full#supplementary-material
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Keywords: Terminalia catappa, melanoma, antimetastasis, matrix metalloproteinases-2, Wnt/βcatenin pathways
Citation: Chang C-K, Chu S-C, Huang J-Y, Chen P-N and Hsieh Y-S (2022) Terminalia catappa leaf extracts inhibited metastasis of A2058 and A375 melanoma cells via downregulating p-Src and β-catenin pathway in vitro. Front. Pharmacol. 13:963589. doi: 10.3389/fphar.2022.963589
Received: 07 June 2022; Accepted: 02 September 2022;
Published: 27 September 2022.
Edited by:
Chien-Shan Cheng, Shanghai Jiao Tong University, ChinaReviewed by:
Hong Zhang, Johns Hopkins Medicine, United StatesShalom Nwodo Chinedu, Covenant University, Nigeria
Mohammad Ali, State University of New York-Binghamton, United States
Copyright © 2022 Chang, Chu, Huang, Chen and Hsieh. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Pei-Ni Chen, peini@csmu.edu.tw; Yih-Shou Hsieh, csmcsh@csmu.edu.tw