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Introduction

Esophageal carcinoma is the 6th frequent cause of cancer-related mortality worldwide (1), and esophageal squamous cell carcinoma (ESCC) accounts for ESCC) accounts for 90% of all esophageal carcinoma cases in Asian countries (2). Although surgical techniques and peri-operative management have progressed, the prognosis for patients with ESCC remains poor (3). Thus, the identification of molecular therapeutic targets which may be used in the treatment of ESCC is one of the most promising avenues of research that lead to an improvement in the survival of patients with this type of refractory cancer. Some of the genetic alterations associated with the development or progression of ESCC have been described (4). However, few of these genes have been demonstrated to be associated with the biological or pathological characteristics of ESCC. Therefore, the identification of novel genes associated with the progression of ESCC is imperative.

The mammalian target of rapamycin (mTOR/p70S6 kinase (p70S6K) signaling pathway is an important intracellular signal transduction pathway, which is closely associated with cell survival and cell proliferation in many types of cancer. Studies have demonstrated that cell proliferation and cell cycle-related proteins (such as cyclin B1 and p27) (4,5), cell apoptosis-related proteins [such as cellular inhibitor of apoptosis protein 1 (cIAP1) and caspase-3] (6,7) and the key proteins [p70S6K and eukaryotic translation initiation factor 4E-binding protein 1 (4EBP1)] (8). Studies have shown that the mTOR pathway activates protein translation and regulates protein synthesis, which is the central regulator of cell growth. mTOR plays an important role in determining cell, tissue and organ size. The mTOR pathway is a key pathway that regulates cell growth and proliferation, which integrates signals from nutrient molecules, energy states and growth factors to regulate a large number of life processes, including autophagy (9–10), ribose body biosynthesis (11,12) and metabolism (13). p70S6K is the main downstream target of mTOR which make an important role in the translation initiation, protein synthesis, cell cycle, cell migration in the mTOR/p70S6K pathway (19). The dysregulation of the pathway is associated with a variety of human diseases, including cancer (14,15), diabetes (16) and leukemia (17,18). 4EBP1 is a downstream effector molecule of mTOR, through which (by phosphorylation) mTOR regulates cancer growth, proliferation and survival. cIAP1 is an inhibitor of apoptosis protein that inhibits apoptosis mainly by inhibiting the activity of caspase-3/7 and the role of nuclear factor (NF)-κB (20). Caspase-3 is the most important terminal cleavage enzyme in the process of apoptosis. It is the terminal executive molecule downstream of the caspase cascade, which is the intersection of the death receptor pathway and mitochondrial pathway. Thus, caspase-3 is also known as death protease (21). Furthermore, the mTOR/p70S6K pathway plays an important role in the growth, proliferation and anti-apoptosis of ESCC (22).

The anticancer activity of cardiac glycosides (the main active ingredients in toad venom) has been a subject of investigation since 1967. Emerging evidence now suggests that cardiac glycosides are able to inhibit cell proliferation and induce the apoptosis of various tumor cell lines. Bufalin, a major bufadeinolide-like cardiac glycoside isolated from the skin and parotid venom glands of the toad (23), has been shown to induce cancer cell death through apoptotic pathways and has been investigted experimentally in a number of types of cancer.

The aim of this study was to evaluate the anti-tumor effects of bufalin by examining its effects on the mTOR/p70S6K signaling pathway and on cell apoptosis in a mouse model of ESCC created by the orthotopic transplanation of tumor cells. We examined the effects of bufalin on the expression of apoptosis-related proteins in order to determine the anti-tumor mechanisms of action of bufalin on a molecular level.

Materials and methods

Cells, antibodies and reagents

The ESCC cell line, ECA109, was provided by the Scientific Research Center of the Fourth Hospital of Hebei Medical University (Hebei, China). A total of 36 Nu/Nu nude mice (half male and half female, aged 4–6 weeks, weighed 18–22 g) purchased from Vital River Laboratory Animal Technology Co., Ltd. (Beijing, China). Our study was approved by the Ethics Committee of the Fourth Hospital of Hebei Medical University. Bufalin was obtained from Shanghai Yuanye Biotechnology Co., Ltd. (Shanghai, China) and rapamycin was purchased from the Beyotime Institute of Biotechnology (Shanghai, China). mTOR, p70S6K, 4EBP1, cIAP1, caspase-3, Bad, Bcl-2, β-actin upstream and downstream primers were all from Shanghai Sangon Biological Engineer ing Co., Ltd., (Shanghai, China). Rabbit anti-mTOR (1612-1), p70S6K (T2921), p-p70S6K (ab2571), 4EBP1 (1557-1), p-4EBP1 (2250-1), cIAP1 (3302-1), Bad (1541-1), Bcl-2 (1017-1) and β-actin monoclonal antibodies, and rat anti-active caspase-3 monoclonal antibody (1476-1) were obtained from Epitomics (Burlingame, CA, USA). The Alpha Innotech UV gel imaging system was from Alpha Innotech Co., (San Leandro, CA, USA) and the Odyssey two-color infrared laser imaging system was from LI-COR Biosciences (Lincoln, NE, USA) The inverted phase contrast microscope was from Nikon (Tokyo, Japan).

Cell culture and tumor model

The ECA109 cells were seeded in 10% fetal bovine serum (FBS) of RPMI-1640 medium and incubated at 37°C in a 5% CO2 incubator. The medium was changed once every 2 to 3 days. A total of 36 nude mice were inoculated with ECA109 cancer cells (each with 0.2 ml injected subcutaneously into the right side of the axillary region) on the first day. The mice were provided with adequate food and water and kept in an environment with a temperature of 21±2°C and relative humidity of 30–70%. No ECA109 cancer cells were injected during feeding. The mice were allowed to feed for 15 days and until the size of the tumors reached approximately 1 cm3. The mice were then randomly divided into 6 groups (n=6 per group) as follows: the model group (saline-treated group), the low-dose bufalin group (0.5 mg/kg, BL group), the medium-dose bufalin group (1 mg/kg, BM group), the high-dose bufalin group (1.5 mg/kg, BH group), the rapamycin group (RAPA group) and the combination group (administered bufalin and rapamycin; BR group). The nude mice were injected for 30 days intraperitoneally according to the dose in each group every day apart from the combination group (once every other day). The mice in the model group were injected with 0.2 ml saline once a day, and those in the rapamycin group were injected with 50 μg/kg rapamycin. The nude mice were sacrificed by cervical dislocation at the end of the treatment period. The tumors were then removed and approximately 0.5 cm3 of the tumor was cut and placed in a refrigerator at −80°C for use in RT-PCR and western blot analysis. The remaining parts of the tumors were fixed in formalin for H&E staining, TUNEL and immunohistochemistry. The tumor inhibition rate was calculated as follows: tumor inhibition (%) = (mean tumor volume of model group - mean tumor volume of intervention group)/mean tumor volume of model group ×100%.

Morphological analysis

The graded ethanol-dehydrated, paraffin-embedded, hematoxylin and eosin (H&E)-stained, xylene-cleared tissue sections were sliced at 4 μm. The H&E-stained sections were observed under a microscope (Axio Scope.A1; Carl Zeiss (Shanghai) Management Limited, Shanghai, China), and the groups were divided according to the necrosis range, that is, focal necrosis, a large area of necrosis, or a larger area of necrosis.

TUNEL assay

The tumor tissues were fixed in 10% neutral formalin, dehydrated, paraffin-embedded and sectioned prior to TUNEL staining. The sections were then digestived with 20 μg/ml proteinase K (Beyotime Institute of Biotechnology) for 15 min. The apoptotic index in the tumor tissue was detected using the ApopTag Peroxidase In Situ Apoptosis Detection kit (EMD Millipore; Bilerica, MA, USA). The results of TUNEL staining were observed under a microscope (Axio Scope.A1; Carl Zeiss (Shanghai) Management Limited). The positive staining was observed in DAB coloring liquid. A total of 10 high power field (HPF) were selected to calculate the proportion of positive cells randomly and the apoptotic index (AI) was the number of positive cells in 100 cells.

RT-PCR

Total RNA was extracted using TRIzol reagent (Sangon Biotech (Shanghai) Co., Ltd., Shanghai, China) and the integrity of RNA was determined using the Alpha Innotech Gel imaging system. Total RNA were reverse transcribed into cDNA. At the end of PCR amplification, the PCR amplification products were confirmed and analyzed. The primers for mTOR, p70S6K, 4EBP1, cAIP1, caspase-3 primers were verified by NCBI and β-actin was used as an internal reference gene. The primer sequences were as follows: mTOR (318 bp) forward, 5′-AGTGGACCAGTGGAAAC AGG-3′ and reverse, 5′-TTCAGCGATGTCTTGTGAGG-3′; p70S6K (188 bp) forward, 5′-TACTTCGGGTACTTGGTAA-3′ and reverse, 5′-GATGAAGGGATGCTTTACT-3′; 4EBP1 (156 bp) forward, 5′-ACCGGAAATTCCTGATGGAG-3′ and reverse, 5′-CCCGCTTATCTTCTGGGCTA-3′; cIAP (245 bp) forward, 5′-TCCCAGGTCCCTCGTATCAA-3′ and reverse, 5′-ATCCAGCATCAGGCCACAAC-3′; caspase-3 (116 bp) forward, 5′-TCATTATTCAGGCCTGCCGTGGTA-3′ and reverse, 5′-ATGCATACAAGAAGTCGGCCTCCA-3′. The reaction conditions were as follows: for mTOR: 95°C for 5 min, 95°C for 30 sec, 60.1°C for 30 sec, 72°C for 30 sec; 37 cycles, 72°C for 10 min; for p70S6K: 95°C for 5 min, 95°C for 45 sec, 48°C for 45 sec, 72°C for 1 min, 37 cycles; 72°C for 5 min; for 4EBP1: 95°C for 5 min, 95°C for 30 sec, 48°C for 30 sec, 72°C for 30 sec, 37 cycles; 72°C for 10 min; for cIAP1: 95°C for 5 min, 95°C for 30 sec, 60°C for 50 sec, 72°C for 30 min, 35 cycles; 72°C for 5 min; caspase-3 was 95°C for 5 min, 95°C for 30 sec, 56°C for 45 sec, 72°C for 1 min, 35 cycles; 72°C for 10 min. The results were observed using the Alpha Innotech UV gel imaging system and the grayscale value was then calculated as follows: relative expression amount = grayscale value of target gene/grayscale value of β-actin.

Western blot analysis

Approximately 30 mg fresh tumor tissue was ground and place on ice. This was followed by the addition of 300 μl ice-cold lysis buffer and 2 μl PMSF. The samples were then centrifuged at12,000 × g at 4°C for 15 min. The proteins (50 μg) were denatured at 95°C in metal bath and then subjected to SDS-PAGE and transferred onto PVDF membranes. The membranes were then incubated with the primary antibodies, mTOR, p70S6K, p-p70S6K, 4EBP1, p-4EBP1, cIAP1, active caspase-3, Bad and Bcl-2 (dilution, 1:2,000), diluted in TBST overnight at 4°C in a shaker. We then used an Odyssey two-color infrared laser imaging system to capture and analyze the images after washing the membranes 3 times with TTBS and the grayscale value was then determined.

Immunohistochemistry

Immunohistochemistry was carried out using the EnVision™ immunohistochemistry kit (Agilent Technologies, Santa Clara, CA, USA) according to the manufacturer's instructions. This was followed by the addition of antibodies (mTOR, p70S6K, p-p70S6K, 4EBP1, p-4EBP1, cIAP1, active caspase-3, Bcl-2 and Bad) to the slices and incubation at room temperature for 150 min, paying attention to ensure that the antibodies were in full contact with the tissues. We determined the location of mTOR, p70S6K, p-p70S6K, 4EBP1, p-4EBP1, cIAP1, active caspase-3, Bcl-2 and Bad on the cell membrane, nucleus or cytoplasm. The staining intensity was scored as follows: no color corresponding to 0, canary yellow corresponding to 1, pale brown corresponding to 2, tan corresponding to 3; the percentage of positive cells was negative corresponding to 0, positive cells <10% corresponding to 1, positive cells between 11–50% corresponding to 2, positive cells between 51–75% corresponding to 3, and positive cells >75% corresponding to 4. The product of staining intensity and the percentage of positive cells was negative (−) corresponding to 0, weakly positive (+) corresponding to 1–4, moderate positive (++) corresponding to 5–8 and strong positive (+++) corresponding to 9–12.

Statistical analysis

One-way analysis of variance (ANOVA) was used to determine the differences between the 6 groups and multiple comparisons between groups were made using the Student-Newman-Keuls (SNK) test. The experimental data of the results of immunohistochemistry were examined using the Kruskal-Wallis H test and multiple comparisons between groups were made using the Nemenyi test. The results were considered statistically significant at a vaue of P<0.05.

Results

No obvious abnormalities were observed as regards the dietary habits of the nude mice diet and the mental state of the mice in all the groups (model, BL, BM, BH, RAPA and BR) during the course of medication (P>0.05) (Table I). There were no significant differences in the body weight of the mice in each group prior to treatment (P>0.05), and even post-treatment (P>0.05) (Table II). The tumor size of the mice in each group (model, BL, BM, BH, RAPA and BR) was 1.778±0.176, 1.714±0.188, 1.115±0.124, 0.713±0.122, 0.699±0.079 and 0.506±0.076 cm3, respectively and the tumor inhibition rate was 4.1, 37.6, 60.1, 60.9 and 71.7%, respectively (Fig. 1, Table III). It proved that bufalin has obvious antitumor effect.

Figure 1 The change of nude mice tumor volume before and after treatment. *P<0.05 vs. model.

Table I The mental state and dietary habits of the nude mice during the course of medication.

Table I

The mental state and dietary habits of the nude mice during the course of medication.

Groups	Mental state	Dietary habits
		Fodder consumption (g)	Post-treatment
Model	Good	3.2±0.3	4.5±0.1
Low-dose bufalin	Good	3.4±0.3	4.4±0.3
Medium-dose bufalin	Good	3.5±0.2	4.6±0.3
High-dose bufalin	Good	3.8±0.2	4.9±0.2
Rapamycin	Good	3.4±0.3	4.6±0.5
Combination	Good	3.6±0.2	4.6±0.1

[i] Values are expressed as the means ± SD (n=3). Pairwise comparision between each group, P>0.05.

Table II Average weight of nude mice in the transplanted model before and after treatment.

Table II

Average weight of nude mice in the transplanted model before and after treatment.

Groups	Body weight (g)
	Pre-treatment	Post-treatment
Model	20.9±2.4	27.9±3.0
Low-dose bufalin	20.8±1.5	28.2±1.9
Medium-dose bufalin	20.8±2.1	27.9±2.9
High-dose bufalin	20.9±2.7	28.1±2.8
Rapamycin	20.9±1.9	27.9±2.0
Combination	20.8±2.1	27.8±2.6

[i] Values are expressed as the means ± SD (n=3). Pairwise comparision between each group, P>0.05.

Table III Average tumor volume and inhibiting rate of the transplanted mode before and after treatment.

Table III

Average tumor volume and inhibiting rate of the transplanted mode before and after treatment.

Groups	Tumor volume (cm3)		Tumor inhibition (%)
	Pre-treatment	Post-treatment
Model	0.199±0.103	1.778±0.176	–
Low-dose bufalin	0.194±0.111	1.714±0.188	3.6
Medium-dose bufalin	0.206±0.099	1.115±0.124a	37.3
High-dose bufalin	0.197±0.079	0.713±0.122a	59.9
Rapamycin	0.192±0.126	0.699±0.079a	60.7
Combination	0.203±0.121	0.506±0.076a	71.5

{ label (or @symbol) needed for fn[@id='tfn3-ijmm-40-02-0357'] } Values are expressed as the means ± SD (n=3).

a P<0.05, vs. model group.

Morphology of cells in tumor tissue

We observed the morphological changes in the tumor tissue isolated from the nude in each group mice with orthotopically transplanted tumors. The hematoxylin and eosin (H&E)-stained sections were observed under a microscope. Tumor necrosis was evident in all the groups, apart from the model group in which necrosis was hardly evident. The tissues from the BL group exhibited the most extensive focal necrosis; the tisues from the BM group exhibited a large area of necrosis; the tissues from the BH, RAPA and BR groups exhibited large areas of necrosis and cancer cell clumps were scattered in the necrotic tissues (Fig. 2).

Figure 2 The morphology of nude mice transplanted tumor (by H&E staining, x20 magnification). (A) Model; (B) low-dose bufalin; (C) medium-dose bufalin; (D) High-dose bufalin; (E) rapamycin and (F) combination.

Bufalin promotes cell apoptosis in ESCC tumor tissue, as shown by TUNEL assay

Apoptotic nuclei were stained brownish yellow. The apoptotic indexes of each treatment groups (BL, BM, BH, RAPA and BR) were significantly higher (13.67, 16.17, 10.83, 10.33 and 8.5%) than those of the model group (2.17%); those of the BM group were the highest (Fig. 3).

Figure 3 Apoptotic morphology of nude mice transplanted tumor cells, the arrow in the image refers to the apoptotic cells (by TUNEL labeling, ×40 magnification). (A) Model; (B) Low-dose bufalin; (C) medium-dose bufalin; (D) high-dose bufalin; (E) rapamycin and (F) combination. (G) Apoptotic index of cells in transplanted tumors.

Bufalin affects the expression of apoptosis-related genes

The mRNA expression levels of mTOR and cIAP1 gradually decreased in the treatment groups (BL, BM, BH, RAPA and BR) compared to the model group, whereas the mRNA expression levels of caspase-3 gradually increased; significant differences were observed (P<0.05). It should be noted that no significant differences were observed between the model and BL groups (P>0.05), and between the BH and RAPA groups (P>0.05). The mRNA expression levels of p70S6K and 4EBP1 did not differ significantly between the groups (P>0.05; model, BL, BM, BH, RAPA and BR) (Fig. 4).

Figure 4 The expression of mTOR, P70S6K, 4EBP1, cIAP1 and caspase-3 mRNA in orthotopic transplanted tumor of human esophageal squamous cell carcinoma (ESCC) in nude mice. (A) RT-PCR analysis of mTOR, P70S6K, 4EBP1, cIAP1 and caspase-3 mRNA levels in each proup. (B) The relative expression of mTOR, P70S6K, 4EBP1 in each proup. (C) The relative expression of cIAP1 and caspase-3 in each proup. *P<0.05 vs. mode.

Bufalin increases the expression of apoptotic proteins, and decreases that of anti-apoptotic proteins

The protein expression levels of mTOR, p-p70S6K, p-4EBP1, cIAP1 and Bcl-2 gradually decreased in the treatment groups (BL, BM, BH, RAPA and BR) compared to the model group. However, the protein levels of caspase-3 and Bad gradually increased, with significant differences between the each groups (P<0.05). Again, it should be noted that no significant differences were observed between the model and BL groups (P>0.05), and between the BH and RAPA groups (P>0.05). No statistically significant differences were observed in the protein expression levels of p70S6K and 4EBP1 (P>0.05) between the (model, BL, BM, BH, RAPA and BR) (Fig. 5).

Figure 5 The expression of mTOR, P70S6K, p-P70S6K, 4EBP1, p-4EBP1, cIAP1, active caspase-3, Bad, Bcl-2 protein in orthotopic transplanted tumor of human esophageal squamous cell carcinoma (ESCC) in nude mice. (A) Western blotting of mTOR, P70S6K, p-P70S6K, 4EBP1, p-4EBP1, cIAP1, active caspase-3, Bad and Bcl-2 protein levels in each groups. (B) The relative expression of mTOR, P70S6K, p-P70S6K, 4EBP1, p-4EBP1 in each groups. (C) The relative expression of cIAP1, active caspase-3, Bad and Bcl-2 in each groups. **P<0.05 vs. model; #P<0.05 vs. medium-dose bufalin; *P<0.05 vs. rapamycin and high-dose bufalin.

Immunohistochemistry assay

The immunoreactive scores for mTOR, p-p70S6K, p-4EBP1, cIAP1 and Bcl-2 gradually decreased in each treatment group (BL, BM, BH, RAPA and BR) (Fig. 6), whereas those for active caspase-3 and Bad gradually increased compared to the model group (Fig. 7), with significant differences observed (P<0.05). However, no significant differences were observed between the model and BL groups (P>0.05), and between the BH and RAPA groups (P>0.05). The immunoreactive scores for p70S6K, 4EBP1 did not differ significantly between the groups (model, BL, BM, BH, RAPA and BR (P>0.05) (Fig. 8).

Figure 6 Immunohistochemical staining of mTOR, p-P70S6K, p-4EBP1, cIAP1 and Bcl-2 in nude mice transplanted tumor (×40 magnification). (A) Model; (B) low-dose bufalin; (C) medium-dose bufalin; (D) high-dose bufalin; (E) rapamycin and (F) combination.

Figure 7 Immunohistochemical staining of active caspase-3, Bad in nude mice transplanted tumor (×40 magnification). (A) Model; (B) low-dose bufalin; (C) medium-dose bufalin; (D) high-dose bufalin; (E) rapamycin and (F) combination.

Figure 8 Immunohistochemical staining of P70S6K, 4EBP1 in nude mice transplanted tumor (x40 magnification). (A) Model; (B) low-dose bufalin; (C) medium-dose bufalin; (D) high-dose bufalin; (E) rapamycin and (F) combination.

Discussion

Bufalin is one of the main components extracted from toad venom and is used in traditional Chinese medicine (TCM) (23). It is known to exert anti-tumor effects. Bufalin has been shown to exert anti-tumor, diuretic, cardiac, blood pressure-promoting, anesthetic, anti-inflammatory, anti-radiation and antitussive effects and has been shown to inhibit the Na+/K+-ATP enzyme (23). Krenn and Kopp suggested that the most effective composition of bufalin had digoxin-like immunoreactive effects (23). Bufalin is an effective antitumor agent and has been applied in the therapy of diverse malignant tumors (24). Studies have shown that cardiac glycoside drugs inhibit the proliferation of tumor cells and induce apoptosis in gastric cancer (25), prostate cancer (26), liver cancer (27), endometrial cancer (28), ovarian cancer (28) and colon cancer (29). Lee et al found that bufalin inhibited tumor growth by inhibiting endothelial cell proliferation and angiogenesis (30). Xia et al found that the anti-tumor effects of bufalin were associated with the induction of tumor cell apoptosis (31). Yamada et al found that the anti-tumor effects of bufalin were associated with the induction of tumor cell differentiation (32). Currently, the exact mechanisms responsble for the anti-tumor effects of bufalin are not clear. Xu et al indicated that bufalin is an active compound of the traditional Chinese medicine, Chansu, which exhibits significant anti-tumor activities in many solid tumors and leukemia cell lines (33). Qiu et al also demonstrated that bufalin inbibits the proliferation and invasion of hepatocellular carcinoma cells (34). Our study demonstrated that bufalin exerts anti-tumor effects. However, further research is required to fully determine the effects of bufalin in ESCC.

A previous study suggested that bufalin decreased the phosphorylation levels of extracellular signal-regulated kinase (ERK) in vitro, while the levels of non-phosphorylation ERK were not affected. It was suggested that the anti-tumor effects of bufalin were associated with the activation of ERK (35).

Numerous studies have confirmed that the mTOR/p70S6K signaling pathway plays a central role in cell survival, growth and proliferation, and is significantly activated in a variety of tumors, such as breast cancer, prostate cancer and cervical cancer, and has become a novel target in cancer therapy (36–41). mTOR is a member of the PIKK superfamily and is an untypical serine/threonine protein kinase. It is highly conserved evolutionary (42). mTOR regulates protein synthesis, cell growth, and proliferation and apoptosis (43). p70S6K is an important key factor downstream of the mTOR pathway. It is a substrate which activates mTOR directly and promotes protein synthesis. p70S6K is phosphorylated into p-p70S6K through mTOR and the translational activity of p-p70S6K is approximately 100-fold greater than that of p70S6K (44). The activation process of p70S6K is very complex, and it requires at least 7 serine/threonine phosphorylation sites (45). These can be divided into two regions, one for Thr389, Thr229 and Ser404; phosphorylation at Thr389 could be directly activated protein kinase. The second is responsible for the regulation of kinase activity at the C-terminus (Ser411, Ser424, Ser418 and Thr421) (45).

4EBP1 is a negative regulator of protein translation translation in mammalian cells. When cells are exposed to external stimuli, 4EBP1 is inactivated by activated mTOR which causes dissociation from eIF-4E (46). In the presence of mTOR inhibitors, 4EBP1 is dephosphorylated and combines with eIF-4E, inhibiting the initiation of translation. In our study, we measured the tumor volume in nude mice following treatment with low- or high-dose bufalin and bufalin in combination with rapamycin. Compared with the model group, tumor growth was decreased in the BM, BH, RAPA and BR groups, whereas tumor growth was not significantly altered in the BL group. This suggests that bufalin inhibits tumor growth at medium and high doses, whereas it has no significant inhibitory effect at lower doses. The results from western blot analysis and immunohistochemistry indicated that the expression of p-p70S6K and p-4EBP1 decreased following treatment with bufalin and/or rapamycin. The most significant decrease was observed in the BR (combination) group. Of note, the expression of p70S6K and 4EBP1 exhibited no significant change. We thus inferred that bufalin inhibited the phosphorylation and activity of p70S6K and 4EBP1 by inhibiting the mTOR/p70S6K pathway. Bufalin and rapamycin may thus inhibit the mTOR/p70S6K pathway synergistically. Therefore, it can be concluded that the anti-tumor effects of bufalin are mediated via the mTOR/p70S6K pathway and via the inhibition of the activity of p70S6K and 4EBP1. The results of RT-PCR demonstrated that the mRNA expression levels of p70S6K, 4EBP1 were not significantly altered in each group. Bufalin inhibited the phosphorylation of p70S6K, which further confirmed our above conclusions.

Recently, it has been shown that the occurrence of malignant tumor is associated with the dysregulation of apoptosis. Inhibitor of apoptosis proteins (IAPs) are a type of highly conserved proteins which regulate the activity of caspase-3/-7/-9 and immune signals to inhibit the process of apoptosis. cIAP1 inhibits apoptosis mainly by suppressing the activity of caspase-3/-7 and NF-κB (20). cIAP1 plays a pivotal role in a large number of malignancies. In China, the incidence of esophageal cancer is high and reports on cIAP1 in esophageal cancer are limited. Xu et al suggested that a high expression of cIAP1 in ESCC was associated with the chemosensitivity of esophageal cancer (47). Zhang et al found that the overexpression of XIAP in esophageal cancer and the downregulation of XIAP was associated with RNA interference and could enhance the chemotherapeutic sensitivity of esophageal cancer (48). In addition, caspase proteases exist in the cytoplasm and can cleave peptide bonds in aspartic acid residue of the target protein specifically (48). Caspase-3 is the most critical terminal cleavage enzyme during apoptosis, which is the terminal executive molecule downstream of caspase cascade. Caspase-3 is the intersection of the death receptor pathway and mitochondrial pathway. Thus, caspase-3 is also known as the death protease (21). Normally, caspase-3 exists in the cell cytoplasm as zymogen form (pro-caspase) When the zymogen is stimulated by an apoptotic signal, pro-caspase can be activated to translate into active-caspase-3, which is involved in the process of apoptosis.

The Bcl-2 family plays a critical role in the process of apoptosis, as it consists of anti-apoptotic proteins (Bcl-2, Bcl-xL, Bcl-w and ced-9) and pro-apoptotic proteins (Bad, Bax, Bak and Bcl-xS). Bcl-2 is anti-apoptotic and can inhibit cell apoptosis, prolonging the life of cells, whereas Bad promotes cell apoptosis (49). In this study, apoptosis was detected by TUNEL assay. We found that the apoptotic index was highest in the BL and BM groups, it was decreased in the BH group. It was thus suggested that bufalin induces apoptosis mainly at low- and medium-doses, while it can kill tumor cells directly at high doses, leading to large areas of necrosis. In the RAPA and BR groups, large areas of necrosis were observed, but the apoptotic index was lower than that of the BL and BM groups. The results of RT-PCR, western blot analysis and immunohistochemistry revealed that the mRNA and protein expression of cIAP1 gradually decreased in each group, suggesting that bufalin exerted a dose-dependent effect. That is to say, with the increasing concentration of bufalin, the expression of cIAP1 decreased, being lowest in the BR group. Simultaneously, the expression of caspase-3 mRNA and active caspase-3 protein increased in each group. With the inreasing concentrations of bufalin, the expression of Bad increased, whereas that of Bcl-2 decreased. Thus, bufalin exerted pro-apoptotic effects by regulating the expression levels of Bcl-2 and Bad. There was a certain dose-dependent effect. We speculated that bufalin and rapamycin induced apoptosis synergistically. The anti-tumor effects of bufalin may be associated with the down-regulation of cIAP1 and the upregulation of of caspase-3 in esophageal cancer cells. As cIAP1 can inhibit the activation of caspase-3, with the decrease in the expression of cIAP1, the caspase-3 was activated in the esophageal cancer cells. In this way, caspase-3 is activated and can promote the initiation of the apoptotic process in esophageal cancer cells.

In conclusion, our study demonstrates tht bufalin exerts palpable anti-tumor effects on orthotopically transplanted ESCC tumors in nude mice. Bufalin decreased the levels of phosphorylated p70S6K and 4EBP1, whereas the levels of p70S6K and 4EBP1 were not affected. We thus suggest that bufalin inhibits tumor growth by suppressing the activation of p70S6K and 4EBP1. Bufalin also decreased the expression of cIAP1 and Bcl-2, and it upregulated active caspase-3 and Bad simultaneously. Thus, the induction of tumor cell apoptosis may be one of the critical antitumor mechanisms of bufalin.

Acknowledgments

This study was supported by the National Natural Science Foundation of China. The authors would like to thank the research specialist staff of Laboratory Animal Center at the Fourth Hospital of Hebei Medical University. Finally, we would also like to thank the professors and technical staff of the Department of Pathology in the Fourth Hospital of Hebei Medical University.

References