Introduction
Esophageal cancer (EC) ranks eighth among the cancers with the highest incidence rate worldwide. The reason is that prominent symptoms rarely appear until the advanced stages of the disease. About 20–30% of patients with EC have distant metastasis at the time of the initial diagnosis [
1], which impedes the treatment of EC. The disease has a poor prognosis, with its 5-year survival rate of only 13% [
2]. To lengthen survival in patients with EC, chemotherapy is considered the most important treatment. However, the toxicity of most chemotherapeutic agents to normal tissues presents a major obstacle to successful treatment. Therefore, a highly effective therapy with reduced side effects urgently needed.
Many previous studies proved that combining prescription medications and herbal medicine can improve anticancer properties and reduce side effects [
3‐
5]. Saffron is a Chinese traditional herb. Crocetin, the major constituent of saffron, has drawn research interest for its multiple pharmacological effects, including anticancer properties [
6,
7]. Cytotoxicity in various cancer cell lines, including human gastric cells [
8], colon cancer cells [
9], and cervical cancer cells [
10] has been confirmed. Our previous studies [
11] exerted a marked inhibitory effect on the growth of KYSE-150 cells. Cisplatin (DDP) combination therapy is considered the cornerstone of treatment of many cancers. However, after the initial use of this combined treatment, patients gradually became less sensitive to cisplatin, particularly after a long-term treatment or recurrence. Considerable efforts have been directed toward improving the therapeutic efficacy of cisplatin. Numerous studies combined an anticancer herb with cisplatin to enhance the therapeutic effect of cisplatin [
12,
13], given that many herbs exhibit either no toxicity or reduced toxicity to humans. The present study aimed to investigate whether combined crocetin and cisplatin exerts a synergistic effect on KYSE-150 cells and explore its underlying mechanism by examining phosphatidylinositol 3-kinase (PI3K)-protein kinase B (AKT), mitogen-activated protein kinases (MAPKs), and p53/p21 in KYSE-150 cells, which significantly influence the occurrence, progression, and prognosis of tumors.
Materials and methods
Chemicals and reagents
Crocetin (C20H24O4, molecular weight, 328.4) and dimethyl sulfoxide (DMSO) were supplied by MP Biomedicals (Santa Ana, CA, USA). Crocetin was dissolved in DMSO, stored at − 20 °C, and diluted in a medium prior to each experiment. The final DMSO concentration did not exceed 0.1% throughout the study. Dulbecco’s Modified Eagle’s Medium (DMEM), penicillin, and streptomycin were purchased from Gibco (Gibco Life Technologies, Carlsbad, CA, USA). Pifithrin-α-HBr (ab120478) (PFT-α) was supplied by Abcam (Abcam, Cambridge, UK). 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2-H-tetrazolium bromide (MTT) was purchased from Sigma-Aldrich (St. Louis, MO, USA). Annexin V-FITC/PI Apoptosis Assay Kit was obtained from BestBio (BestBio Co., Ltd, Shanghai, China). Bicinchoninic Acid Protein Assay Kit was purchased from Beyotime Institute of Bioengineering (Jiangsu, China). Horseradish peroxidase-conjugated goat anti-rabbit antibodies were obtained from Wuhan Boster Biological Technology, Ltd. (Wuhan, Hubei, China).
Cell culture
The esophageal squamous carcinoma KYSE-150 cell line was purchased from Japanese Collection of Research Bioresources Cell Bank (JCRB, Osaka, Japan). The KYSE-150 cells were cultured in DMEM supplemented with 10% fetal bovine serum (Zhejiang Tianhang Biological Technology Stock Co., Ltd., Zhejiang, China), 100 units/mL of penicillin and 100 μg/mL of streptomycin cells were maintained at an atmosphere of 5% CO2 and 95% air at 37 °C. When cells in the logarithmic growth phase were used for experiments, each test was performed at least in triplicate.
MTT assay to assess cell proliferation
The effect of crocetin and cisplatin on cell viability was measured by MTT assay as described in a previous study [
14]. KYSE-150 cells were seeded in 96-well plates at a density of 6000 cells/well in complete DMEM and then incubated at 37 °C. After 24 h, the cells were incubated with varying concentrations of cisplatin (0.25, 0.5, 1, 2, 4, and 8 μg/mL) or combined 200 μmol/L of crocetin and 2 μg/mL of cisplatin for 24, 48, and 72 h. After incubation, the medium was aspirated carefully, and the 96-well plate was gently washed with phosphate buffered saline (PBS). Cells were then incubated with MTT. After 4 h, the supernate was discarded, and formazan was dissolved in DMSO. The absorbance of each well was measured at 570 nm in a microplate reader (Tecan Austria GmbH, Grödig, Austria).
Morphologic detection of apoptosis
Cell apoptosis induced by crocetin and cisplatin was determined using the Annexin V-FITC/PI apoptosis kit in accordance with the manufacturer’s instructions. Cells were plated in a 12-well plate at a density of 1.2 × 10
5 cells/well and then treated with different agents (control, 200 μmol/L of crocetin, 0.2 μg/mL of cisplatin, 200 μmol/L of crocetin + 0.2 μg/mL of cisplatin) for 48 h. The cells were subsequently washed thrice with ice-cold PBS and incubated with 5 μL Annexin V-FITC, 10 μL of PI mixed in a 400 μL of buffer solution for 15 min at 37 °C in a humidified atmosphere in the dark. The plate was gently washed three times with PBS. A fluorescent apoptotic cell morphology was observed under an inverted phase contrast microscope and then photographed. Annexin V- or PI-positive cells were identified as apoptotic cells. The numbers of apoptotic cells were expressed as percentages of total cells of each field, and at least three fields were calculated [
15,
16].
Measurement of mitochondrial membrane potential (MMP)
The MMP was measured by inverted-phase contrast microscopy by using the fluorescent dye Rhodamine 123 (Rh123). KYSE-150 cells were plated into 12-well plates and then exposed to crocetin or/and cisplatin for 48 h. After incubation, cells were washed with PBS three times and then incubated with 2 μmol/L Rh123 for 30 min at 37 °C in a humidified atmosphere in the dark. The plate was gently washed three times with PBS. Images of the cells were finally obtained under an inverted phase contrast microscope and analyzed using Image-Pro Plus 6.0.0.260 (Media Cybernetics, USA).
Western blot analysis
After treatment with different drugs for 48 h, the KYSE-150 cells were harvested and lyzed in an ice-cold lysis buffer (1× PBS; 1% NP40; 0.1% SDS; 5 mm EDTA; 0.5% sodium deoxycholate; 1% PMSF) for 30 min. The lysate was cleared by centrifugation at 14,000×
g for 15 min at 4 °C. The supernatant extract was collected and quantified for protein by using the BCA protein assay kit. Equal quantities of cell protein were subjected to electrophoresis in 10 or 12% sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE). The protein was then transferred to polyvinylidene difluoride (PVDF) membranes and subsequently blocked using 5% bovine serum albumin for 1 h at room temperature and was then incubated overnight with primary antibodies at 4 °C. The blots were washed three times with Tris-buffered saline (Guangzhou Whiga Biotechnology Co., Ltd., Guangzhou, China) containing 0.05% Tween-20 (Wuhan Boster Biological Technology, Ltd.) and then incubated with horseradish peroxidase-conjugated anti-rabbit antibodies for 1 h at room temperature. The protein bands were detected by electrochemiluminescence, and the band intensity was measured using ImageJ 1.46r (National Institutes of Health, Bethesda, MA, USA). Each experiment was repeated at least three times. The Western blot antibodies used are listed in Table
1.
Table 1
Antibodies used in Western blot analysis
PI3K | mAb | 1:1000 | Cell signaling |
p-PI3K | mAb | 1:2000 | Cell signaling |
AKT | mAb | 1:1000 | Cell signaling |
p-AKT | mAb | 1:1000 | Cell signaling |
ERK1/2 | mAb | 1:1000 | Cell signaling |
p-ERK1/2 | mAb | 1:1000 | Cell signaling |
JNK | mAb | 1:1000 | Cell signaling |
p-JNK | mAb | 1:1000 | Cell signaling |
p38 | mAb | 1:1000 | Cell signaling |
p-p38 | mAb | 1:1000 | Cell signaling |
p53 | pAb | 1:1000 | Cell signaling |
p21 | mAb | 1:1000 | Cell signaling |
Bax | mAb | 1:1000 | Abcam |
Bcl-2 | mAb | 1:1000 | Abcam |
Cleaved caspase-3 | mAb | 1:2000 | Cell signaling |
GAPDH | mAb | 1:1000 | Millipore |
Statistical analysis
All data were collected from at least three experiments and expressed as mean ± SEM. The differences among groups—control, crocetin, cisplatin, and combination of agents—were analyzed by one-way ANOVA, followed by the least significant difference post hoc test in SPSS 16. (SPSS, Inc., Chicago, IL, USA). p < 0.05 was considered statistically significant.
Discussion
Cisplatin is a basement chemotherapy for EC, and initial cisplatin responsiveness is highly effective. However, some patients can eventually fall into relapse with cisplatin resistance over time. In addition, the side effect of cisplatin is another issue in cisplatin treatment in the clinical setting. Thus, effective chemotherapy with reduced side effects is urgently needed for EC patients. A growing number of studies have focused on whether the combination of prescription medications and anticancer herbs could achieve a synergistic effect and reduce side effects [
12,
13]. Crocetin, a sort of carotenoid, has reportedly exhibited biomedical properties, including anticancer properties as well as less or non-toxicity to normal cells [
8,
17,
18]. In the present study, we investigated whether crocetin combined cisplatin has synergistic effect in KYSE-150 cells and explored the underlying mechanism. The results we obtained indicated that the combination of crocetin and cisplatin significantly inhibited cell proliferation and induced cell apoptosis in KYSE-150 cells. Mechanistically, this synergistic effect exhibits a close association with the up regulation of p53/p21 expression as well as the activation of mitochondria- mediated apoptosis pathway, as manifested by the overexpression of p53 and p21, loss of MMP, upregulation of Bcl-2, and downregulation of cleaved caspase-3. The synergistic effect was also partially blocked after pifithrin-α was added.
A previous study has shown that tumorigenesis has a close relationship with the cell signaling pathway. In this study, we analyzed the expression of PI3K/AKT, MAPKs, and p53/p21 pathways in KYSE-150 cells. The PI3K/AKT pathway is an intracellular signaling pathway that significantly affects cell proliferation. The phosphorylated PI3K can activate AKT. The activated AKT can further phosphorylate BAD on Ser-136 and prompt it to dissociate from the Bcl-2/Bcl-xl complex, ultimately resisting cell apoptosis. The PI3K/AKT pathway has been proven to be related to the occurrence, progression, and prognosis of EC, as well as resistance to chemotherapy and radiotherapy [
19‐
22]. Moreover, the inhibitor of the PI3K/Akt pathway significantly suppressed cell proliferation and induced cell apoptosis via suppressed Bcl-xl expression. Thus, the PI3K/AKT pathway could be potentially used for cancer treatment. Our results indicated that cisplatin decreased p-PI3K but not p-AKT expression (Fig.
5). These results may be associated with the resistance of KYSE-150 cells to cisplatin [
23]. PI3K/AKT expression was significantly lower in the combined crocetin and cisplatin group than in the cisplatin-only group; however, the reduction was not as much in the crocetin-only group. Thus, we concluded that the PI3K/AKT signaling pathway does not induce the response for combined crocetin and cisplatin to exert a synergistic effect on the KYSE-150 cells.
In addition, we determined the expression of mitogen-activated protein kinases in KYSE-150 cells. MAPKs include the extracellular signal-regulated kinase 1 and 2 (ERK1/2), JNK, and p38, which are involved in cell proliferation, differentiation, mitosis, and apoptosis. The activation of ERK1/2 phosphorylated Bim and/or Bad reduced the sensitivity of cells to apoptosis and promoted cell proliferation [
24]. The phosphorylated p38 and JNK could induce cell apoptosis; however, several studies found that p38 could also induce cell proliferation and anti-apoptosis, particularly in an inflammatory environment [
25,
26]. Overexpression of ERK1/2, p38, and JNK occurred in esophageal cancer patients [
27‐
29]. However, suppression of the expression of ERK1/2 and p38 induced prominent cell apoptosis in carcinoma cells [
30,
31]. The expression of Aquaporin 5 was positively correlated with drug resistance in colon cancer, and silencing of Aquaporin 5 suppressed p38 MAPK signaling and improved drug resistance in colon cancer cells. In addition, using a p38 inhibitor could also exert a similar effect [
32]. Therefore, the recovery of the normal expression of MAPKs is important for EC treatment. In the current study, the combined crocetin and cisplatin treatment markedly down-regulated the levels of p-ERK1/2 and p-p38 but showed no significant decrease compared with the crocetin-only treatment (Fig.
6). These results suggested that the synergistic effect of crocetin and cisplatin was not attributable to the MAPK pathway either.
Finally, we explored the p53/p21 pathway in the KYSE-150 cells. P53 is encoded by the tumor suppressor gene p53, which plays an important role in the regulation of cell cycle, cell apoptosis, and inhibition of angiogenesis. P21, widely known as cyclin-dependent kinase inhibitor 1, regulates cell cycle progression. Activated p21 could induce the arrest of cell growth. P21 is highly controlled by p53. An increasing number of evidence confirmed that the occurrence of EC exhibits a close correlation with high mutant p53 expression and low p21 expression [
33]. However, mutant p53 lost it normal function. Thus, restoring the normal function of p53 is key to cancer treatment. The results of our study indicated that the expression levels of p53 and p21 were higher with the combined crocetin and cisplatin treatment than with the single treatments. Adding pifithrin-α, a wild-type p53 inhibitor, partially restored cell proliferation and rescued the cells from death. Moreover, p53 induced cell apoptosis via up-regulated expression of Bid, another pro-apoptotic protein in the Bcl-2 family. Overexpression of p53 could trigger mitochondria-mediated apoptosis pathway and induce the disruption of MMP, downregulation of Bcl-2, cyto-C release, and activation of caspase-3. Our results indicated that compared with the single treatments, combined crocetin and cisplatin markedly increased cleaved caspase-3 expression and decreased Bcl-2 expression. However, adding pifithrin-α partially blocked this mitochondria-mediated apoptosis pathway. Therefore, we concluded that the synergistic effect of combined crocetin and cisplatin was closely associated with the p53/p21 pathway.
Conclusion
To date, our study is the first to demonstrate that the synergistic effects of crocetin and cisplatin on inhibition of cell proliferation and pro-apoptotic effect in KYSE-150 cells. The underlying mechanism was associated with the up regulation of the p53/p21 pathway and induction of the mitochondria-mediated apoptosis pathway, as shown by the disruption of MMP. Crocetin combined cisplatin also decreased Bcl-2 expression and increased cleaved caspase-3 expression. However, as our study examined only one cell line, more cell lines and in vitro experiments should be tested. In addition, the mechanism under the synergistic effect of crocetin and cisplatin still need further investigate. How to modulate p53/p21 pathway to obtain the synergistic effect? Such as MDM2, which is an important regulator of the p53 and function as ubiquitin ligase that recognizes the N-terminal trans-activation domain and as an inhibitor of p53 transcriptional activation. Nevertheless, our study clearly indicated that combined crocetin and cisplatin exhibits a synergistic effect and can provide a potential treatment for EC patients.
Authors’ contributions
TL and HW designed the study. SL performed the experiments and wrote the articles. XS helped to performed the experiments and collected the data, TO and YQ participated in the statistical analysis. All authors read and approved the final manuscript.