Molecular Medicine Reports Molecular Medicine Reports 1791-2997 1791-3004 D.A. Spandidos 10.3892/mmr.2019.10115 mmr-19-06-4964 Articles Salidroside suppresses the metastasis of hepatocellular carcinoma cells by inhibiting the activation of the Notch1 signaling pathway LuLinlin 1 * LiuShousheng 2 3 * DongQuanjiang 2 XinYongning 3 4 5 Department of Clinical Medicine, Qingdao University, Qingdao University Hospital, Qingdao, Shandong 266003, P.R. China Central Laboratories, Qingdao Municipal Hospital, Qingdao, Shandong 266071, P.R. China Digestive Disease Key Laboratory of Qingdao, Qingdao, Shandong 266071, P.R. China Department of Gastroenterology, Qingdao Municipal Hospital, Qingdao, Shandong 266011, P.R. China Department of Infectious Disease, Qingdao Municipal Hospital, Qingdao, Shandong 266011, P.R. China Correspondence to: Dr Yongning Xin, Department of Infectious Disease, Qingdao Municipal Hospital, 1 Jiaozhou Road, Qingdao, Shandong 266011, P.R. China, E-mail: xinyongning@163.com

Contributed equally

 062019 02042019 19 6 4964 4972 17072018 26032019 Copyright © 2019, Spandidos Publications 2019

Salidroside (SDS) is a phenylpropanoid glycoside isolated from Rhodiola rosea L. It exhibits multiple pharmacological properties in clinical medicine and has been commonly used in traditional Chinese medicine. The present study investigated the inhibitory effects of SDS on tumor invasion and migration, and the expression of metastasis-related genes in highly metastatic hepatocellular carcinoma (HCC) cells (MHCC97H) in vitro. The underlying mechanisms of SDS on the tumor metastasis were also explored. SDS was found to significantly reduce wound closure areas and inhibit cell migration. In addition, SDS markedly inhibited the invasion of these cells into Matrigel-coated membranes. SDS markedly downregulated the expression of Notch1, Snail, COX-2, MMP-2, MMP-9 genes and upregulated the expression of E-cadherin in a dose-dependent manner. Furthermore, SDS inhibited the expression of the Notch signaling target genes, Hey1, Hes1 and Hes5. On the whole, the findings of this study suggest that SDS inhibits HCC cell metastasis by modulating the activity of the Notch1 signaling pathway.

 salidroside hepatocellular carcinoma migration invasion Notch1 signaling pathway Introduction

Hepatocellular carcinoma (HCC) is the most commonly diagnosed primary tumor of the liver, ranking third worldwide in terms of the most lethal types of cancer (1,2). While there are some treatment options available for patients, such as surgical intervention, radiotherapy, locoregional therapy and chemotherapy, the rates of metastasis and relapse remain high for patients with HCC (3,4). Therefore, there is currently an urgent need for improved treatment options in clinical practice.

Salidroside (SDS) acts as a phenylpropanoid glycoside and is one of the most potent antioxidant ingredients that can be isolated from Rhodiola rosea L. It commonly grows at high altitudes and may be found in parts of Asia, Eastern Europe and Canada (5,6). SDS functions as an adaptogen that provides non-specific resistance by suppressing physical, chemical and biological stressors in the body, and has been used as a hepato-protective herb in traditional Chinese medicine for decades (5).

In recent years, SDS has been reported to possess numerous medicinal properties, including antitumor, anti-inflammatory, anti-viral, anti-radiation, antioxidative stress and fatigue-reducing properties (7–16). Most notably, the anticancer properties of SDS have been extensively reported by researchers in both in vitro and in vivo models. SDS has been shown to significantly inhibit the growth of lung, breast and liver cancer through the promotion of the activation of cellular apoptotic pathways, and to inhibit breast tumor growth in vivo (6,17–22). In addition, SDS has been shown to inhibit metastasis, as Sun et al demonstrated that SDS inhibited the migration and invasion of HT1080 human fibrosarcoma cells (23). However, there is limited information about the role of SDS in preventing the metastasis in other forms of cancer, and its underlying mechanisms of action remain unknown.

Notch signaling is highly conserved and is often activated in many types of tumors, playing complex roles in tumor development and metastasis (24–30). Previously, Zhou et al (31) reported Notch1 as a novel candidate biomarker for assessing patient prognosis, as well as for the molecular targeted therapy of HCC. This is due to the high expression of Notch1 in HCC tumor tissues, which has been associated with tumor size, tumor grade, metastasis, venous invasion and TNM stage. Patients with a high Notch1 expression were shown to have significantly shorter overall survival times (31).

The downregulation of Notch1 has been previously found to decrease the invasiveness of HCC cells in vitro (32), which is partially attributed to the activation of the Notch1/Snail/E-cadherin pathway (33–36). E-cadherin acts as a homotypic epithelial cell-cell adhesion molecule with anti-invasive properties in certain types of cancer (37–39). The Notch1/matrix metalloproteinase (MMP) pathway has also been found to play an important role in HCC development, as MMPs are proteolytic enzymes in the extracellular matrix (ECM) that contribute to tumor invasion, angiogenesis and metastasis (40–42). Previously, the downregulation of Notch1 in pancreatic cancer and lingual squamous cell carcinoma was shown to inhibit tumor invasion by suppressing the expression of MMP-2 and MMP-9 (28,29,32). In addition, an inhibitor of the Notch signaling pathway effectively inhibited the invasion of HCC cells via MMP-2 and MMP-9 suppression (32), confirming that the Notch1 signaling is closely associated with the metastasis of HCC.

In the present study, we demonstrate that SDS suppresses the metastasis of highly metastatic HCC cells. Genes involved in EMT and metastasis are consisted regulated. Notably, Notch1 signaling activity is inhibited by SDS. Taken together, the findings of this study suggest that SDS suppresses the metastasis of HCC cells through suppression of the activation of the Notch1 signaling pathway.

 Materials and methods <sec> <title>Reagents and antibodies

SDS (purity, >99%) was purchased from the National Institute for the Control of Pharmaceutical and Biological Products (Beijing, China). SDS was dissolved in water and filtered through a 0.22-µm filter prior to use. Hairy and enhancer of split 1 (Hes1; cat. no. BM4488) polyclonal antibodies were purchased from Boster Biological Co. (Wuhan, China). Hairy/enhancer-of-split related with YRPW motif 1 (Hey1; cat. no. 19929-1-AP) and hairy and enhancer of split 5 (Hes5; cat. no. 22666-1-AP) polyclonal antibodies were purchased from ProteinTech Biological Co. (Wuhan, China). Cyclooxygenase (COX)-2 (cat. no. KGYT1073-6), E-cadherin (cat. no. KGYT1453-6), MMP-2 (cat. no. KGYT2798-6) and MMP-9 (cat. no. KGYT1892-6) polyclonal antibodies were purchased from KeyGEN BioTech Corp. (Nanjing, China). Snail (cat. no. bs-21598R) and Notch1 (cat. no. bs-1335R) polyclonal antibodies were purchased from Bioss Biological Co. (Beijing, China). DMEM was purchased from the Gibco; Thermo Fisher Scientific Inc. (Waltham, MA, USA). FBS was purchased from the ExCell Biology Company (Shanghai, China). All other chemicals were of analytical grade and were commercially available.

 Cells and cell culture

The MHCC97H cells (cat. no. KG340) were obtained from KeyGEN BioTech Corp. the HMCC97H cells were cultured in DMEM supplemented with 10% fetal bovine serum (FBS) in a humidified incubator at 37°C with 5% CO2. The cells were harvested following trypsinization (0.25% Trypsin-EDTA) and washed with phosphate-buffered saline (PBS). The cells were subcultured when the cell density reached 80–90% confluency.

 Scratch wound closure assay

For the detection of cell migration, the HMCC97H cells were seeded onto a 6-well plate and cultured at 37°C for 24 h. When the cell density reached 60% confluency, the monolayer was scraped away with a sterile tip, as previously described (43). The remaining cells were washed with PBS, and cultured with new medium with 1, 2, or 4 µg/ml of SDS at 37°C for 24 h. Cell migration into the denuded area was quantified using a computer-assisted inverted microscope (IX71; Olympus Corporation, Tokyo, Japan; magnification, ×200).

 Transwell assay for in vitro migration

HMCC97H cell migration was measured using Matrigel-coated Transwell inserts. The cells were cultured in serum-free DMEM at 37°C for 24 h before being trypsinized and seeded at 5×104 cells per upper chamber in 100 µl serum-free DMEM with 1, 2 or 4 µg/ml SDS. The 24-well plate containing the Transwell was cultured in a humidified incubator at 37°C and 5% CO2 for 24 h. Cells in the upper side of the insert membrane were rubbed using a cotton swab. Cells that had migrated to the underside of the insert membrane were stained with 0.1% crystal violet solution for 30 min at 37°C, rinsed in PBS, air-dried, and observed under an inverted microscope (IX71; Olympus Corporation) equipped with a camera to count the number of migrated cells (magnification, ×200). Three fields per insert were scored and averaged.

 In vitro invasion assay

The invasion of the HMCC97H cells in vitro was determined using Matrigel-coated Transwell inserts, as previously described (44). Serum-free DMEM with 2-fold diluted Matrigel (30 µl/well) was placed into the upper chamber of the Transwell filter and incubated for 2 h at 37°C for gelling. Subsequently, 5×104 cells were seeded in the upper chamber and cultured at 37°C for 24 h. The invasion of the cells was assessed using the same techniques as those used for cell migration described above.

 Reverse transcription-quantitative PCR (RT-qPCR)

RT-qPCR was used to determine the expression levels of Notch1, Hes1, Hes5, Hey1, COX-2, Snail and E-cadherin in the SDS-treated HMCC97H cells. The cells were incubated with serum-free DMEM containing 1, 2 or 4 µg/ml SDS for 24 h. Subsequently, the cells were trypsinized, washed in PBS, and total RNA was extracted using TRIzol reagent (Thermo Fisher Scientific Inc.) according to the manufacturer's instructions. First-strand cDNA was synthesized with a reverse transcription kit (Thermo Fisher Scientific Inc.) according to the manufacturer's instructions and used as the template for RT-qPCR. GAPDH was selected as the reference for internal standardization. The primers P1 and P2 specific of GAPDH, P3 and P4 specific of Hes1, P5 and P6 specific of Hes5, P7 and P8 specific of Hey1, P9 and P10 specific of COX-2, P11 and P12 specific of Snail, P13 and P14 specific of MMP-2, P15 and P16 specific of MMP-9, and P17 and P18 specific of E-cadherin (Table I) were designed to amplify the specific fragments of all the genes. qPCR was performed on an ABI 7500 real-time PCR system (Applied Biosystems, Foster City, CA, USA) using the 2X SYBR Premix Ex Taq™ kit (Takara, Shiga, Japan). PCR was carried out in a total volume of 20 µl, containing 10 µl 2X SYBR Premix Ex Taq™, 0.4 µl ROX Reference Dye II (50X), 1 µl diluted cDNA, 0.2 µl primers (20 mmol/l) and 8.4 µl of DEPC-treated water. The thermal profile for RT-qPCR was 94°C for 15 sec, followed by 40 cycles of 94°C for 5 sec, 60°C for 15 sec and 72°C for 35 sec. All reactions were run in triplicate. Dissociation curve analysis of the amplicons was performed at the end of each PCR to confirm that only one PCR product was amplified and detected. Data were analyzed with the comparative Cq method (2−∆∆Cq) based on Cq values for each gene and GAPDH to calculate relative mRNA expression levels (45).

 Western blot analysis

The HMCC97H cells were cultured with serum-free DMEM with 1, 2, or 4 µg/ml SDS for 24 h. The cells were washed 3 times with ice-cold PBS and harvested in lysis buffer. The lysate was centrifuged at 12,000 × g for 15 min to collect the supernatant. Bicinchoninic acid (BCA) was used to determine the protein concentrations. Subsequently, 40 µg of each sample was loaded onto 12% sodium dodecyl sulfate (SDS)-polyacrylamide gels for electrophoresis and transferred onto nitrocellulose membranes. The membranes were blocked with 4% BSA in PBS at room temperature for 2 h prior to incubation with primary antibodies, which included anti-Notch1 (1:1,000), anti-Hey1 (1:1,000), anti-Hes1 (1:1,000), anti-Hes5 (1:1,000), anti-Snail (1:1,000), anti-COX2 (1:1,000), anti-E-cadherin (1:1,000), anti-MMP-2 (1:1,000), anti-MMP-9 (1:1,000), and anti-GAPDH (1:2,000). The membranes were incubated with the primary antibodies overnight at 4°C and washed 4 times with PBS containing 0.1% Tween-20 (PBST). The membranes were then incubated with HRP-conjugated anti-mouse/rabbit IgG (cat. no. bs-0368R-HRP/bs-0369M-HRP; BIOSS, Beijing, China) diluted at 1:5,000 in PBS for 1 h at room temperature before being washed with PBS-T and detected using the ECL reagent (KeyGEN BioTech Corp.). The signal intensity of each band was quantified with ImageJ software (version 1.6.0; National Institutes of Health, Bethesda, MD, USA), and the results were normalized to those of GAPDH.

 Statistical analysis

Data are presented as the means ± standard errors of the mean (SEM) from 3 or more independent experiments and were evaluated with analysis of variance (ANOVA) followed by Dunnett's test for multiple comparisons. P<0.05 was considered to indicate a statistically significant difference.

 Results <sec> <title>SDS suppresses the migration of HMCC97H cells in vitro

The scratch test and Transwell assay were used to determine the effects of SDS on the migration of the HMCC97H cells. As shown in Fig. 1A, the wound closure was 69.2% complete in the absence of SDS. Following treatment with SDS, the wound closure levels were significantly lower at 58.2, 42.5 and 33.4% in the cells treated with 1, 2 and 4 µg/ml SDS, respectively. The migration of the HMCC97H cells was significantly suppressed by SDS, as shown by Transwell assay. As shown in Fig. 1B, cell migration was reduced to 65.31, 39.68 and 28.12% (relative to the control) following 24 h of treatment with 1, 2 and 4 µg/ml SDS, respectively. These results demonstrated that SDS can effectively suppress HCC cell migration in a concentration-dependent manner.

 SDS suppresses the invasion of HMCC97H cells in vitro

The Matrigel-coated Transwell assay was used to examine the effects of SDS on the invasion of the HMCC97H cells. As shown in Fig. 2, SDS treatment significantly suppressed the invasion of the HMCC97H cells in vitro. Following 24 h of treatment with SDS, the number of invaded cells had decreased to 64.5, 29.0 and 17.5% when treated with 1, 2 and 4 µg/ml SDS, respectively. These results indicated that SDS effectively suppressed the invasion of the HMCC97H cells in a concentration-dependent manner.

 SDS decreases the expression of Notch1, Snail, COX-2, MMP-2 and MMP-9, whereas it upregulates the expression of E-cadherin in the HMCC97H cells

Western blot analysis was performed to investigate protein expression in the HMCC97H cells following treatment with SDS. Since Snail, COX-2, MMP-2, MMP-9 and E-cadherin are closely related to the metastasis of tumor cells (43,46–48), we also investigated the effects of SDS on these genes in the HMCC97H cells. As shown in the Figs. 3 and 4, expression levels of Notch1, Snail, COX-2, MMP-2 and MMP-9 were significantly lower following treatment with SDS (P<0.05). Moreover, E-cadherin expression was markedly increased following treatment with SDS (P<0.05).

 SDS inhibits the activation of the Notch1 signaling pathway

Since the Notch1 signaling pathway is closely related to tumor metastasis and SDS can inhibit metastasis (49), we hypothesized that SDS may function through the Notch1 signaling pathway. The activity of the Notch signaling pathway was thus assessed by the expression of its downstream genes, including Hey1, Hes1 and Hes5. As shown in Fig. 5, treatment with SDS significantly reduced the expression levels of these genes (P<0.05). This indicates that SDS likely inhibits the metastasis of cancer cells by halting the activation of the Notch1 signaling pathway.

 Discussion

The Notch1 signaling pathway plays an important role in the differentiation, proliferation and apoptosis of cells during early development, and may eventually contribute to tumorigenesis (50,51). Notch1 plays a paradoxical role in different types of cancer as it is upregulated in several types of tumors and plays complex roles in tumor development and metastasis (24–30). Previously, Notch1 expression has been shown to be associated with the decreased overall survival of patients with breast, colorectal and liver cancers (31,52,53). SDS has been reported to display anticancer properties both in vivo and in vitro. A previous study demonstrated that SDS inhibited the migration and invasion of HT1080 cells (23). Considering the hepatoprotective role of Rhodiola rosea L. in traditional Chinese medicine, in the present study, we aimed to determine whether SDS can inhibit the metastasis of HCC via the Notch1 signaling pathway.

Tumor metastasis leads to the expression of two gene sets, including invasion promotors and invasion suppressors (54,55). E-cadherin acts as a homotypic homophilic epithelial cell-cell adhesion molecule that can inhibit tumor cell invasion (37–39). During the invasion and metastasis of epithelial tumor cells mediated by Notch1, Snail expression is upregulated, while E-cadherin is downregulated. This indicates that Notch1 may mediate metastasis by disrupting the normal expression profiles of Snail and E-cadherin (33).

In the present study, we investigated the effects of SDS on the migration properties of highly invasive HCC cells via the scratch wound closure test and Transwell assay. The results from scratch wound closure assay revealed that wound closure was suppressed by SDS in a concentration-dependent manner (Fig. 1A). Similarly, the results of Transwell assay revealed that cell migration was suppressed by SDS in a concentration-dependent manner (Fig. 1B). This indicates that SDS can inhibit the migration of cancer cells in a concentration-dependent manner. In order to determine the possible underlying mechanisms, we detected the activity of the Notch1 signaling pathway. RT-qPCR was conducted to investigate the transcription of Notch1, the Notch1 signaling pathway relevant genes, Hey1, Hes1 and Hes5, and the migration-associated genes, Snail, COX-2 and E-cadherin, in HMCC97H cells. The expression levels of Notch1, Hey1, Hes1, Hes5, Snail and COX-2 in the HMCC97H cells were significantly decreased following treatment with SDS (Figs. 3 and 5). In addition, the expression of the migration-related gene, E-cadherin, in the HMCC97H cells was markedly increased following treatment with SDS (Fig. 3). Western blot analysis was also conducted to examine the protein expression levels of Notch1, Hey1, Hes1, Hes5, Snail, COX-2 and E-cadherin in the HMCC97H cells following treatment with SDS. SDS was found to significantly inhibit the activation of Notch1, Hey1, Hes1, Hes5, Snail and COX-2, while it markedly promoted the activation of E-cadherin (Figs. 4 and 5). These results indicate that SDS may suppress the migration of HMCC97H cells by inhibiting the activation of the Notch1 signaling pathway.

MMPs are a family of proteolytic enzymes that contribute to tumor cell invasion, migration and tumor angiogenesis by degrading the basement membrane and other ECM components (23,56–58). The endothelial cell activities, which are essential for new vessel development, can be blocked with MMP inhibitors. In return, MMP inhibitors likely halt the proliferation and invasion of tumor cells (59). Previously, the overexpression of tumor suppressor tissue inhibitors of metalloproteinases (TIMPs) was shown to downregulate the expression of MMP-2 and inhibit the invasion and metastasis of cancer cells (58). Previous studies have indicated that the Notch1 signaling pathway can regulate the activities of MMP-2 and MMP-9 in pancreatic cancer, lingual squamous cell carcinoma and breast cancer (28–30). In HCC cells, the downregulation of Notch1 decreases the expression and proteolytic activities of MMP-2 and MMP-9 (31). This suggests that the Notch1/MMP-2/MMP-9 axis may participate in tumor cell invasion. Previously, Sun et al demonstrated that the SDS decreased MMP-2 and MMP-9 activities, and inhibited the invasion of HT1080 cells (23); however, it remains unknown as to whether the SDS-attributed inhibition of MMP-2 and MMP-9 activities occurs via the Notch1 signaling pathway.

In this study, we examined the effects of SDS on the invasion of HMCC97H cells, and also aimed to elucidate the underlying mechanisms. The results of Transwell assay revealed that SDS suppressed the invasion of MHCC97H cells in a concentration-dependent manner, and the expression levels of MMP-2 and MMP-9 in the MHCC97H cells were significantly reduced following treatment with SDS. In addition, the expression levels of MMP-2 and MMP-9 in the MHCC97H cells were also reduced after SDS treatment. Previous studies have shown that Notch1 mediates the migration and invasion of tumor cells through regulation of MMP-2 and MMP-9 expression and that Notch1 signaling pathway activity can be suppressed with SDS treatment (32,60). Therefore, SDS likely inhibits the migration and invasion of tumor cells by down-regulating the Notch1 signaling pathway.

In conclusion, the findings of this study suggest that SDS suppresses the migration and invasion of HMCC97H cells in a concentration-dependent manner by inhibiting the activation of the Notch1 signaling pathway. The results suggest that SDS may be an effective anticancer agent with minimal adverse effects. Considering the importance of the Notch1 signaling pathway, this may be an excellent biomarker for the development of novel therapies for HCC; however, more profound research into the Notch1 signaling pathway and its role in cancer metastasis is required.

 Acknowledgements

Not applicable.

 Funding

The present study was supported by the Young Scientist Research Foundation of Medjaden Bioscience Limited (grant no. MJR20160051) and the National Natural Science Foundation of China (grant nos. 31770837 and 31800660).

 Availability of data and materials

All data generated or analyzed during this study are included in this published article.

 Authors' contributions

LL and SL conducted the experiment, LL, SL, and QD analyzed the data. LL and SL wrote the manuscript, YX designed the present study and revised the manuscript.

 Ethics approval and consent to participate

Not applicable.

 Patient consent for publication

Not applicable.

 Competing interests

The authors declare that they have no competing interests.

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SDS suppresses the migration of HMCC97H cells in vitro. (A) The migration of the HMCC97H cells was quantified by measuring wound closure areas before and after injury. The wound closure areas were effectively reduced in the groups treated with 2 and 4 µg/ml SDS. (B) Cell migration was quantified under a microscope (magnification, ×200). The numbers of migrated cells were significantly decreased in the groups treated with 1, 2 and 4 µg/ml SDS. All data are presented as the means ± SEM from 3 independent experiments. Asterisks indicate statistically significant differences (*P<0.05 and **P<0.01) compared to the control (0 µg/ml). SDS, salidroside; SEM, standard error of the mean.

SDS suppresses the invasion of HMCC97H cells in vitro. The invasion of the HMCC97H cells was quantified by Matrigel-coated Transwell inserts. Images indicate the invaded cells visualized under a microscope (magnification, ×200) following SDS treatment. The numbers of migrated cells were significantly decreased in the groups treated with 1, 2 and 4 µg/ml SDS. All data are presented as the means ± SEM from 3 independent experiments. Asterisks indicate statistically significant differences (**P<0.01) compared to the control (0 µg/ml). SDS, salidroside; SEM, standard error of the mean.

Effects of SDS on the expression of Notch1, Snail, COX-2, MMP-2, MMP-9 and E-cadherin in the HMCC97H cells. The cells were treated with 1, 2, and 4 µg/ml SDS. (A-F) The expression levels of Notch1, Snail, COX-2, MMP-2, MMP-9 and E-cadherin were measured by RT-qPCR, and the data were normalized to the GAPDH gene as an internal control. Data are presented as the means ± SEM from 3 independent experiments. Asterisks indicate statistically significant differences (*P<0.05 and **P<0.01) compared to the control (0 µg/ml). SDS, salidroside; COX-2, cyclooxygenase-2; MMP, matrix metalloproteinase; SEM, standard error of the mean.

Effects of SDS on the expression of Notch1, Snail, COX-2, MMP-2, MMP-9 and E-cadherin in HMCC97H cells. The cells were treated with 1, 2 and 4 µg/ml SDS. (A-F) The protein expression levels of Notch1, Snail, COX-2, MMP-2, MMP-9 and E-cadherin were measured by western blot analysis. Bands were scanned and quantified and the results were normalized to GAPDH. Data are presented as the means ± SEM from 3 independent experiments. Asterisks indicate statistically significant differences (*P<0.05 and **P<0.01) compared to the control (0 µg/ml). SDS, salidroside; COX-2, cyclooxygenase-2; MMP, matrix metalloproteinase; SEM, standard errors of the mean.

Effects of SDS on the expression of Hey1, Hes1 and Hes5 in HMCC97H cells. The cells were treated with 1, 2 and 4 µg/ml SDS. (A-C) The mRNA expression levels of Hey1, Hes1 and Hes5 were measured by RT-qPCR and the data were normalized to the GAPDH gene as an internal control. (D-F) Hey1, Hes1, and Hes5 protein expression levels were measured by western blot analysis. Bands were scanned and quantified and the results were normalized to GAPDH. Data are presented as the means ± SEM from 3 independent experiments. Asterisks indicate statistically significant differences (*P<0.05 and **P<0.01) compared to the control (0 µg/ml). SDS, salidroside; Hes1, hairy and enhancer of split 1; Hes5, hairy and enhancer of split 5; Hey1, hairy/enhancer-of-split related with YRPW motif 1; RT-qPCR, reverse transcription-quantitative PCR; SEM, standard errors of the mean.

Table I. Sequences of the primers used in this study.

Gene Sequence (5′-3′) Amplicon size (bp)
Notch1 F-TCAGCGGGATCCACTGTGAG
R-ACACAGGCAGGTGAACGAGTTC 104
Hes1 F-CTGAGCACAGACCCAAGTGT
R-GAGTGCGCACCTCGGTATTA 115
Hes5 F-GAAAAACCGACTGCGGAAGC
R-GACGAAGGCTTTGCTGTGCT 184
Hey1 F-CGGCTCTAGGTTCCATGTCC
R-GCTTAGCAGATCCCTGCTTCT 162
COX-2 F-ATAACCCCGCCAAAAGGGG
R-CTGAGTACCAGGTCTGCAGTG 145
Snail F-CGAGTGGTTCTTCTGCGCTA
R-GGGCTGCTGGAAGGTAAACT 160
MMP-2 F-GATGACATCAAGGGCATTCAGGAGC
R-ATCTTTTCCGGGAGCTCAGGCC 254
MMP-9 F-CCAAGGATACAGTTTGTTCCTCGTG
R-GGTTCAGGGCGAGGACCATAGA 177
E-cadherin F-GTCAGTTCAGACTCCAGCCC
R-TGTAGCTCTCGGCGTCAAAG 196
GAPDH F-CATCTTCTTTTGCGTCGCCA
R-TTAAAAGCAGCCCTGGTGACC 202

F, forward; R, reverse; Hes1, hairy and enhancer of split 1; Hes5, hairy and enhancer of split 5; Hey1, hairy/enhancer-of-split related with YRPW motif 1; COX-2, cyclooxygenase-2; MMP, matrix metalloproteinase.