Introduction
Renal cell carcinoma (RCC), which accounts for ~3% of all malignancies, is one of the most lethal urologic malignancies (1) and 20–30% of all patients are diagnosed with metastatic disease (2). Systemic therapeutic strategies for advanced RCC include surgical management, chemotherapy, radiotherapy, immunotherapy and molecular targeted therapy (3–5). Following nephrectomy, 20% of patients will suffer a relapse and develop metastatic (m)RCC (6). Cytotoxic chemotherapy has consistently failed to benefit patients (7) and RCC has been identified as being intrinsically radioresistant (8). Molecular targeted therapy may prolong the life of patients, although they often acquire resistance over time (9,10). In addition, adverse side-effects are often associated with the treatment, including rashes, diarrhea, edema and weight gain (11).
Since the prognosis is poor for patients with advanced RCC or mRCC, there is an urgent demand for further prognostic improvements. As RCC is an immunogenic tumour, it is a putative target for immunotherapeutic intervention strategies (12). Interferon (IFN)-α is an immunotherapeutic agent generated predominantly by monocytes and macrophages, which elicit beneficial effects on human health in a variety of ways. Previous studies revealed that IFN-α modulates the immune response (13), induces apoptosis (14) and directly inhibits the proliferation (15,16) and differentiation of tumour cells (17). As a type I IFN, IFN-α has been used clinically. In addition, IFN-α was recommended as a first-line treatment for clear-cell mRCC in systemic therapy; however, the therapeutic effects of IFN-α monotherapy are limited in duration (18).
The cancer immunoediting theory, which hypothesizes that malignancy results from the imbalance between immunosurveillance and tumour immune escape (19), has reinvigorated much research effort in the field of cancer immunology. Previous studies have revealed that myeloid-derived suppressor cells (MDSCs) are one of the key drivers of tumourmediated immune evasion. MDSCs promote tumour growth via different mechanisms (20,21), and consequently, MDSCs exert a clear prognostic importance in multiple solid tumour types. Newly acquired data support the suitability of circulating MDSCs as a predictive marker for cancer immunotherapy (22).
Lycium barbarum
(Goji berry) has been used in China for 2,000 years. L. barbarum polysaccharides (LBP), derived from the water-soluble portion of extract from L. barbarum, are important bioactive compounds. Previous studies have suggested that LBP may exert a role in a variety of biological processes, including immunomodulation, as an anticancer agent, in enhancing metabolism and in the amelioration of physical fatigue (23,24). Furthermore, novel data revealed that LBP may activate T-cells (25), increase macrophage phagocytosis (26), stimulate the phenotypic maturation of dendritic cells (DCs) with marked immunogenicity (27) and arrest the cell cycle of tumour cells (28). Additionally, a polysaccharide-protein complex markedly suppressed the growth of transplantable sarcomas and enhanced the action of macrophages (26); however, the precise effects of LBP on RCC cells and the underlying molecular mechanisms remain to be elucidated.
In the present study the effects and the mechanism of LBP in combination with IFN-α2b on the murine RCC Renca cell line in vitro and on renal tumour xenografts in vivo were analyzed to provide a basis for the clinical use of LBP and recombinant human IFN-α2b in patients with RCC.
Materials and methods
Murine RCC cell line and cell culture
The murine RCC cell line, Renca, was purchased from Shanghai Cell Bank (Shanghai Xin Yu Biotech Co., Ltd, Shanghai, China). The cells were grown in RPMI-1640 media (Gibco Life Technologies, Carlsbad, CA, USA), including 10% fetal bovine serum (FBS; HyClone, GE Healthcare Life Sciences, Logan, UT, USA), 100 U/ml penicillin and 100 µg/ml streptomycin (Gibco Life Technologies) at 37°C in a humidity-controlled incubator with 5% CO2.
Cell viability assay
The Renca cells (3.0×103 cells/well) were seeded into 96-well plates, cultured for 24 h and stimulated with either fresh RPMI-1640 culture medium, containing either 10% FBS (control), IFN-α2b (1,000, 2,000, 4,000 or 8,000 IU/ml; Furen Pharmaceutical Group Co., Ltd., Beijing, China) or LBP (50, 100, 200 or 400 µg/ml; 70% purity, Xian Plant Bio-Engineering Co., Ltd., Xian, China) for 24, 48 and 72 h. A total of 20 µl 0.5 mg/ml MTT solution (Ameresco, Inc., Framingham, MA, USA) was added to each well, incubated for 4 h and subsequently the culture medium was replaced with 150 µl/well dimethyl sulfoxide (Sigma-Aldrich, St. Louis, MO, USA). The cells were agitated for 10 min to dissolve the purple crystals. The absorbance (A) at 570 nm was analyzed using a microplate reader (680; Bio-Rad Laboratories, Hercules, CA, USA). The cell viability rate (%) was quantified as follows: (Atreated)/(Acontrol) × 100%.
Subsequently, the Renca cells (3.0×103 cells/well) were seeded into 96-well plates and cultured for 24 h in fresh RPMI-1640 culture medium, containing 10% FBS (control), IFN-α2b (4,000 IU/ml), LBP (200 mg/ml) or IFN-α2b (4,000 IU/ml) in combination with LBP (200 mg/ml). The cells were cultured for 24, 48 or 72 h, and the remaining stages were performed, as described above. Each experiment was repeated three times with four wells for each concentration.
Apoptosis assay
The Renca cells (2×105/well) were seeded into 6-well plates and following overnight attachment, were treated with either 10% FBS (control), IFN-α2b (4,000 IU/ml), LBP (200 µg/ml) or IFN-α2b (4,000 IU/ml) in combination with LBP (200 µg/ml), for 48 h. The cells were collected by centrifugation at 1,000 rpm for 5 min at 37°C. The collected cells were washed with ice-cold phosphate buffered saline (PBS) and 1X binding buffer (BD Biosciences, Franklin Lakes, NJ, USA). Subsequently, a 100 µl suspension solution containing 5 µl annexin V-fluorescein isothiocyanate (FITC; BD Biosciences) and 5 µl propidium iodide (PI; Sigma-Aldrich) were incubated at room temperature in the dark for 15 min. Subsequently, 500 µl 1X binding buffer was added and the samples were measured using a FACSVantage SE flow cytometer (BD Biosciences). CellQuest software (BD Biosciences) was used to analyze the flow cytometry data.
Cell cycle analysis
Renca cells stimulated, as described above for the apoptosis assay for 48 h, were treated with trypsin, centrifuged at 800 rpm for 5 min at 37°C and fixed with pre-chilled 75% ethanol for >18 h at 4°C. Following treatment with 1% ribonuclease A (Sigma-Aldrich) for 30 min at 37°C, the cells were stained with 50 µg/ml PI for 30 min at 4°C. A BD FACSVantage SE flow cytometer was used to examine the cell cycle distribution at 490 nm. The proportion of cells in each cycle were analyzed using multicycle DNA content and CellQuest cell analysis software. Each experiment was performed in triplicate.
Western blot analysis
Following seeding the Renca cells (1×106) into a culture flask, the cells were treated, as described for the apoptosis assay, for 48 h. The cells were subsequently lysed in radioimmunoprecipitation assay buffer (Beijing ComWin Biotech Co., Ltd., Beijing, China), containing protease inhibitor, phenylmethylsulfonyl fluoride, and incubated for 30 min on ice. The lysates were ultracentrifuged at 13,800 × g for 15 min at 4°C and the supernatant was collected. The protein concentration was measured using the bicinchoninic acid method (Beyotime Institute of Biotechnology, Haimen, China). The protein lysates (30 µg) were separated by SDS-polyacrylamide gel electrophoresis (Beyotime Institute of Biotechnology) and were transferred onto polyvinylidene difluoride membranes (Amersham Biosciences, Beijing, China) using a wet transfer apparatus. Non-fat milk (5%) was used to block the membranes for 1 h at room temperature, then the membranes were incubated with primary antibodies overnight at 4°C. The antibodies were as follows: Rabbit monoclonal anti-Bcl-2 (1:1,000; cat. no. sc-492), anti-Bax (1:1,000; cat. no. sc-526), anti-cyclin D1 (1:1,000; cat. no. sc-718) and anti-c-Myc (1:1,000; cat. no. sc-764; Santa Cruz Biotechnology, Inc., Santa Cruz, CA, USA), and rabbit polyclonal anti-glyceralde-hyde-3-phosphate dehydrogenase (GAPDH; cat. no. sc-25778; 1:5,000). Subsequently, the membranes were incubated with a 1:2,000 dilution of horseradish peroxidaselabelled secondary antibody (cat. no. CW0103; Beijing ComWin Biotech Co., Ltd.) for 1 h. The protein bands were analyzed using enhanced chemiluminescence (Beijing ComWin Biotech Co., Ltd.) and an Odyssey Two-Color Infrared Imaging system (LI-COR Bioscience, Inc., Lincoln, NE, USA). The blots were re-probed and incubated with anti-GAPDH as a loading control for protein normalization.
Mouse xenograft model treatment
Animal experiments were performed on the basis of the institutional animal care and use committee guidelines at Chongqing Medical University (Chongqing, China). The study was approved by the ethics committee of the First Affiliated Hospital of Chongqing Medical University. A total of 28 male BALB/c mice, aged 4 weeks, were obtained from the Experimental Animal Center of Chongqing Medical University (Chongqing, China) and were fed on a standard sterile laboratory diet for >3 days prior to experiments. The mice were housed 5 per cage in a temperature, humidity, and light/dark cycles-controlled room (temperature: 22±2°C, humidity: 60%, 12 h light/dark cycles) with ad libitum access to food and water. The weight of the mice was 15±0.36 g. Renca cells (2×106) mixed 1:1 with Matrigel (BD Biosciences) in 100 µl PBS were injected subcutaneously into each mouse. When the tumour size reached 40–50 mm3, 28 mice were selected and randomly assigned to either the control, IFN-α2b, LBP or IFN-α2b in combination with LBP groups. IFN-α2b was dissolved in sterile PBS prior to injection and LBP were diluted in sterile PBS for oral administration. IFN-α2b (200 IU/g) was administered by intraperitoneal injection twice weekly for 15 days and LBP were administered by gavage at dosages of 20 µg/g once daily for 15 days. The control and the IFN-α2b alone groups were administered 100 µl sterile PBS by gavage, and the control and the LBP alone groups were administered 100 µl sterile PBS by intraperitoneal injection. The tumour sizes were measured using callipers twice weekly and counted as follows: π/6 × large diameter × (small diameter)2. The body weights were measured twice weekly. On the day following the completion of the 15 day treatment, the animals were sacrificed via cervical dislocation and the tumors were carefully resected, weighed, measured and stored at −80°C.
Detection of the CD11b<sup>+</sup> Gr-1<sup>+</sup> cells from murine bone marrow using flow cytometry and confocal laser scanning microscopy
The femurs and tibias were obtained immediately after the four groups of male BALB/c mice were sacrificed, from which isolated bone marrow cells were labelled using the FITC anti-mouse Ly-6G/Ly-6C and PE anti-mouse CD11b antibodies (Tianjin Sungene Biotech Co., Ltd., Tianjin, China). The cells were subsequently incubated for 30 min at 4°C in the dark. Following two washes, the cells were analyzed using the BD FACSAriaTMII Special Order system (BD Biosciences) and a Leica TCS SP2 laser scanning confocal microscope (Leica, Mannheim, Germany).
Statistical analysis
Statistical analyses were performed using SPSS 17.0 software (SPSS, Inc., Chicago, IL, USA). The data are expressed as the mean ± standard deviation. Multiple comparisons in the interblock were analyzed using a one-way analysis of variance test, and individual comparisons were analyzed using Fisher's least significance difference post-hoc test between the control and treatment groups. P<0.05 was considered to indicate a statistically significant difference.
Results
Inhibition of cell proliferation following treatment with LBP and IFN-α2b in the Renca cells
To investigate the role of LBP and IFN-α2b on the proliferation of the Renca cells, the cells treated with LBP and IFN-α2b were assessed using an MTT assay. To confirm the mode of action of IFN-α2b or LBP alone, and their use in combination, in Renca cells, the absorption was detected at various concentrations and durations. The cell viability rate was subsequently calculated using the above-mentioned equation.
The dose-effect curve demonstrated an effect 48 h following the addition of IFN-α2b at a concentration of 4,000 IU/ml and of LBP at a concentration of 200 µg/ml, whereby the viability of the Renca cells was significantly inhibited. Therefore concentrations of 4,000 IU/ml IFN-α2b and 200 µg/ml LBP were selected for subsequent experiments. IFN-α2b (4,000 IU/ml) in combination with LBP (200 µg/ml) significantly inhibited the cell proliferation in a time-dependent manner (**P<0.01; Fig. 1). The viability of the cells was reduced to 37.0% following this treatment for 48 h. The Renca cells were treated with different concentrations of IFN-α2b alone (1,000, 2,000, 4,000 and 8,000 IU/ml) for 48 h, and the cell viability was 79±1.40, 61±1.30, 40±1.30 and 50±1.24%, respectively. The Renca cells were treated with different concentrations of LBP alone (50, 100, 200 and 400 µg/ml) for 48 h, and the cell viability was 72±1.51, 60±1.21, 41±1.23 and 50±1.11%, respectively.
Combination treatment with LBP and IFN-α2b promotes the apoptosis of Renca cells
To determine the effect of LBP and IFN-α2b on apoptosis in Renca cells, the percentage of cells undergoing apoptosis was confirmed and quantified using an annexin V-FITC/PI assay. The percentages featured in the lower right and upper right quadrant of the histograms represent the early and late apoptotic cells, respectively. Following treatment of the cells, as described above for 48 h, the total percentage of apoptotic cells was 23.26, 34.39 and 56.37% in the IFN-α2b, LBP and IFN-α2b in combination with LBP groups, respectively, compared with the control group (5.43%; *P<0.05 and **P<0.01; Figs. 2A–E). The results demonstrated the anticancer effect of IFN-α2b in combination with LBP in the Renca cells.
Treatment with LBP and IFN-α2b arrests the Renca cell cycle
Treatment with IFN-α2b and LBP inhibited Renca cell growth, which was always associated with cell cycle arrest. Following treatment of the Renca cells with either IFN-α2b, LBP or IFN-α2b in combination with LBP for 48 h, flow cytometry was performed. The results revealed that the combined treatment of the cells with IFN-α2b and LBP resulted in a more marked accumulation in the G0/G1 phase compared with that of the control (P<0.01; Table I and Fig. 3).
Effect of LBP and IFN-α2b on the expression of Renca cell-associated proteins
Cyclin D1, one of the critical cell cycle regulators, promotes the G1/S-phase transition and induces cell proliferation. c-Myc also influences cell cycle regulation, as the overexpression of c-Myc stimulates cell cycle progression, whereas c-Myc downregulation exerts the opposite effect. Bcl-2 protein inhibits target cell apoptosis, whereas the protein Bax enhances target cell apoptosis. Following the treatment of the Renca cells with either IFN-α2b, LBP or IFN-α2b in combination with LBP for 48 h, the expression levels of the above proteins were measured by western blot analysis (Fig. 4A). The results revealed that cyclin D1, c-Myc and Bcl-2 were downregulated, whereas Bax was upregulated, in all treatment groups compared with the control group, and more significant changes were identified in the IFN-α2b in combination with LBP group (Figs. 4B–E).
Combined treatment with LBP and IFN-α2b inhibits tumour growth in a Renca xenograft model
To further determine whether IFN-α2b in combination with LBP inhibits tumour growth in vivo, BALB/c mice bearing Renca tumour xenografts were treated with either IFN-α2b, LBP or IFN-α2b in combination with LBP for 15 days. The doses of drugs used were determined according to a previous study (29). Compared with the control BALB/c mice (Fig. 5A), those treated with IFN-α2b (Fig. 5B) and LBP (Fig. 5C) exhibited a significantly smaller tumour volume. In addition, compared with the groups receiving monotherapy, the tumour volumes in the combination group xenografts (Fig. 5D) were markedly smaller. In conclusion, the data indicated that the antitumor efficacy of LBP combined with IFN-α2b is greater compared with LBP and IFN-α2b alone (Fig. 5E).
Effect of combination treatmetn with LBP and IFN-α2b on the CD11b<sup>+</sup> Gr-1<sup>+</sup> cells in the bone marrow of tumour-bearing mice and the morphology of the CD11b<sup>+</sup> Gr-1<sup>+</sup> cells
MDSCs, which facilitate tumour growth, are one of the crucial negative immune regulators. MDSCs were defined as CD11b+Gr-1+ cells in the mouse. The morphology of the MDSCs was examined using confocal laser scanning microscopy (Fig. 6A). To determine the mechanism of IFN-α2b and LBP on Renca cells in vivo, the proportion of MDSCs in the bone marrow cells from BALB/c mice bearing Renca tumour xenografts were gated. The tumour-bearing mice were treated with either IFN-α2b, LBP or IFN-α2b in combination with LBP for 15 days. The results revealed that the percentages of CD11b+Gr-1+ bone marrow cells were clearly reduced in the treatment groups compared with the control group (Fig. 6B; *P<0.05). Compared with IFN-α2b alone (Fig. 6C) and LBP alone (Fig. 6D) groups, the reduction was more pronounced in the tumour-bearing mice treated with IFN-α2b plus LBP (Fig. 6E; **P<0.01). No significant reduction was observed between the IFN-α2b and LBP alone groups.
Discussion
In the present study, the results revealed that the synergistic immunotherapeutic effects of LBP in combination with IFN-α2b inhibited the proliferation of mouse RCC Renca cells in vitro and in vivo.
RCC is considered to be an immunogenic tumour, for which immunotherapy is one of the systemic therapies. As a multifunctional cytokine, IFN-α intervenes in tumour cell proliferation and apoptosis, and has been used in the treatment of various malignancies. A previous study determined that cell growth was inhibited by treatment with recombinant human IFN-α1b in human nasopharyngeal carcinoma (15). IFN-α markedly inhibits the growth of the pheochromocytoma PC12 line and increases apoptosis (16). Booy et al (30) identified that IFN-α significantly reduces cell growth in eight human pancreatic cancer cell lines. Since the short duration of therapeutic effects and immunotherapeutic efficacy of IFN-α are limited, novel therapeutic strategies for advanced RCC are required.
LBP perform numerous roles, including in immunomodulation and anticancer functions. Previous studies identified that LBP inhibit the proliferation of human QGY7703 hepatoma cells (29), and human MGC-803 and SGC-7901 gastric cancer cells (28). Since IFN-α and LBP operate according to different mechanisms of action in tumour cells, their combined use may potentially offer novel treatment options for RCC; however, the effect and mechanism of LBP and IFN-α2b in combination therapy remains to be elucidated.
To investigate the combined effects of LBP and IFN-α2b in RCC cell lines, the effects of IFN-α2b and LBP on cell viability were initially measured. An MTT assay revealed that there was a marked decrease in cell viability in the Renca cells treated with IFN-α2b or LBP alone; however, cell viability was markedly diminished by co-treatment with LBP and IFN-α2b for 48 h. From these observations, co-treatment with IFN-α2b and LBP appears to be more effective against Renca cell proliferation in vitro compared with treatment with IFN-α2b or LBP alone.
Data have suggested that the antitumor effects of immunotherapeutic drugs are associated with the cell cycle. A previous study demonstrated that T-cells were arrested in the G1-phase by recombinant human IFN-α1b in human nasopharyngeal carcinoma (15). Maeda et al (14) also reported that IFN-α induces cell cycle arrest in the G0/G1 phase in the HuH7 hepatocellular carcinoma cell line.
To elucidate the inhibitory mechanisms of LBP and IFN-α2b in Renca cells, flow cytometric analysis was used to detect the changes in the cell-cycle distribution. The results revealed that the number of Renca cells in the G0/G1 phase were increased following drug treatment. In particular, the ratio of G0/G1 was increased more markedly compared with IFN-α2b or LBP alone. These results were consistent with previous reports using IFN-α treatment in RCC (31), human MGC-803 gastric cancer (28) and human SW480 and Caco-2 colon cancer (32) cells. However, DNA synthesis in human QGY7703 hepatoma cells was affected and arrested in the S phase by LBP action (29). The mechanism of LBP in cancer cells is complicated and differences may result from comparing across varying types of cells.
With the exception of arresting the cell cycle, the effect of certain immunotherapeutic agents against cancer has been largely associated with the induction of apoptosis. Maeda et al (14) reported that IFN-α induces apoptosis in the human HuH7 hepatocellular carcinoma cell line through an IFN-α type-2 receptor-dependent signalling pathway. Markowitz et al (33) reported that the combined use of bortezomib and IFN-α synergistically induced apoptosis in human melanoma cells in melanoma tumour-bearing mice. Additionally, another previous study revealed that LBP suppresses the proliferation of HeLa cells (34) and human QGY7703 hepatoma cells by inducing apoptosis (29). In particular, apoptosis was induced to a greater extent by co-treatment with IFN-α2b or LBP compared with treatment with IFN-α2b or LBP alone. These results suggested that co-treatment with IFN-α2b and LBP suppressed Renca cell proliferation by activating apoptosis.
Emerging evidence has revealed that the cell cycle regulatory- and apoptosis-associated proteins are implicated in the anticancer activity of certain immunotherapeutic agents. To confirm the mechanism of inhibition of proliferation at the protein level, western blot analysis was performed to detect the expression of cyclin D1, c-Myc, Bcl-2 and Bax. In the G0/G1 phase, cyclin D1, which is considered to be one of the predominant cell-cycle regulators, promoted the G1-S phase transition (35). c-Myc is associated with cell cycle regulation, as the expression levels of c-Myc are tightly correlated with cell proliferation. Overexpression of c-Myc stimulates cell cycle progression, whereas Myc downregulation exerts the opposite effect. A previous study suggested that IFN-α inhibits the expression of c-Myc (36). In the present study, the protein expression levels of cyclin D1 and c-Myc were markedly downregulated in Renca cells following treatment with LBP and IFN-α2b, which was as expected, given the known characteristics of the cell-cycle distribution. These results suggested that the combination of LBP and IFN-α2b suppressed Renca cell proliferation to decrease the expression levels of cyclin D1 and c-Myc.
As a proto-oncogene, the Bcl-2 gene inhibits apoptosis. Overexpression of Bcl-2 enhances the resistance of cancer cells to the majority of cytotoxins, whereas downregulation of Bcl-2 expression has been demonstrated to improve chemo-sensitivity in clinical studies with various carcinomas. As a proapoptotic gene, the Bax gene exerts the opposite effects. Zitzmann et al (37) reported that type I IFN-α mediates apoptosis by changing the ratio of antiapoptotic Bcl-2 and Bcl-xL to the proapoptotic molecules Bak and Bax in neuroendocrine tumour cells. A previous study indicated that tumour necrosis factor-α-induced apoptosis was further enhanced by IFN-α by lowering the protein expression of c-Myc in HL-60 cells (38). The expression levels of the Bcl-2 gene were reduced, and the expression of the c-Myc gene was inhibited, by IFN-α in the bone marrow mononuclear cells from chronic granulocytic patients (39).
A previous study revealed that LBP mediates the expression of Bcl-2 and Bax, while inducing apoptosis in human prostate cancer cells (40), and that it also suppresses the expression of the antiapoptotic Bcl-2 gene product in human HL-60 cells (41). Gómez-Benito et al (42) also reported that IFN-α induced myeloma cell apoptosis via the mitochondrial route. Zhu and Zhang (34) reported that the inhibitory effect of LBP on the proliferation of HeLa cells was caused by inducing apoptosis through the mitochondrial pathway.
In the present study, the expression of Bcl-2 was reduced and the expression of Bax was higher in the co-treatment group compared with the control or single drug treatment groups, which may be due to the downregulation of the expression of Bcl-2 at the protein level by the combined use of LBP and IFN-α2b via the mitochondrial pathway.
Subsequently, the combined effect of LBP and IFN-α2b on xenograft tumours was examined, and it was observed that the tumour volume and weight were markedly reduced by co-treatment with LBP and IFN-α2b compared with the control or monotherapy groups. No apparent loss of body weight was observed in the mice treated with the drugs. From these results, it appears that combination therapy with LBP and IFN-α2b will be effective against Renca cell proliferation in vivo.
To further investigate the mechanism of this effect, the population of MDSCs in isolated bone marrow cells was measured using flow cytometry and confocal laser scanning microscopy. MDSCs are a heterogeneous population, comprising progenitor and immature myeloid cells, which are at different stages of maturation and continually differentiate into different types of mature immune cells, including macrophages, DCs and granulocytes. In the mouse, these cells are usually described as CD11b+GR-1+ cells (21). MDSCs inhibit the innate and adaptive immune responses, and immunosuppression is the predominant function of MDSCs. Immune evasion is a hallmark of cancer, and MDSCs are one of the key drivers of tumour-mediated immune evasion. Preclinical data in immunosuppressed murine models suggested that MDSCs are closely associated with tumour progression and the metastatic process, independent of their immunosuppressive properties. The MDSC population promotes tumour growth (20).
Previous studies have revealed that levels of MDSCs are increased in Sokal high-risk chronic myeloid leukemia (43). IFN-α enhanced antitumor efficiency by modulating of the suppressor of cytokine signaling 1 function of CD4 and CD8 T-cells in the context of melanoma (13). Zoglmeier et al (44) reported that recombinant IFN-α diminished the suppressive abilities of MDSCs in tumour-bearing mice. Additionally, a previous study reported that LBP induce phenotypic changes and the maturation of DCs, and enhance host immunity with marked immunogenicity (45). The antitumor mechanism of LBP in H22-bearing mice may be exerted through increasing the numbers of CD4+ and CD8+ T-cells, restoring the function of the immune system (39).
In the present study, combination treatment with LBP and IFN-α2b markedly reduced the ratio of MDSCs in vivo. This indicated that treatment with the combination may decrease the numbers of MDSCs, increase the numbers of macrophages, DCs, granulocytes and CD4 and CD8 T-cells, relieve immunosuppression, and restore innate and adaptive immunity to inhibit the process of tumour growth. However, certain limitations to the present study exist, including the use of only one type of RCC cell line and the in vivo data were generated only from Renca xenograft tumours. Therefore, the investigation of other RCC cell lines is required to further evaluate the clinical potential of the combined use of LBP and IFN-α2b. Additionally, further investigation of the immune cells in the blood and spleen of mice is required.
In conclusion, LBP and IFN-α2b may inhibit the progression of Renca xenografts via the following mechanism: The cells were arrested in the G0/G1 phase, cell proliferation was inhibited, apoptosis was induced, MDSCs were diminished, immunosuppression was relieved, and the innate and adaptive immunity pathways were restored.