Ctive magnification, Olympus).Materials and Methods Animals, Cell Culture, and DrugsSix-week-old

Ctive magnification, Olympus).Materials and Methods Animals, Cell Culture, and DrugsSix-week-old male BALB/c nu/nu nude mice weighing approximately 20 g (Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, PR China) were housed in laminar flow cabinets under specific pathogen-free conditions. The mice were cared for in accordance 25033180 with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals. The experimental protocol was approved by the Shanghai Medical Experimental Animal Care Committee (Approval Number: 2009?556). HCCLM3 human HCC cells [30,31] were grown as a monolayer culture in Dulbecco’s modified Eagle’s medium supplemented with 10 bovine serum albumin. Stable red fluorescent protein (RFP)-expressing HCCLM3 cells[29] were maintained in the same culture as the HCCLM3 cells. All cells were cultured at 37uC in a 5 CO2, 95 air environment in humidified incubators.Orthotopic Nude Mouse ModelThe nude mouse model was established by orthotopic implantation of a histologically intact tumor tissue derived from HCCLM3 or RFP-LM3 cell lines, which had been maintained for more than 80 passages in nude mice. All HCCLM3 and RFPLM3 models exhibited 100 transplantable characteristics and lung metastatic ability as well as various manifestations reminiscent of tumor behavior in patients with HCC. In the first experiment, when the average tumor volume had reached 100 mm3 approximately 1 week after implantation, IFNa (Sinogen, Kexing Bioproduct Company Ltd. Shenzhen, PR China, at a dose of 1.56107 U/kg per injection) or vehicle (normal ��-Sitosterol ��-D-glucoside site saline, NS) was injected subcutaneously daily in two groups of mice (n = 6) for 6 weeks. IFN-a withdrawal study was conducted with daily IFN-a treatment for 3 weeks in one group (six mice) followed by daily NS injection for 3 weeks. All mice were sacrificed after 6 weeks of treatment. Tumor size was assessed using the formula: width 6 length 6 depth 6 p/6. Body weights were measured MedChemExpress 4EGI-1 weekly as a surrogate for toxicity. In another animal study using nude mice without tumors, each group of mice (n = 5 in each group) received daily subcutaneous IFN-a or NS injection for 6 weeks, or IFN-a injection for 3 weeks followed by NS injection for another 3 weeks. After 6 weeks of treatment, all mice were sacrificed.Real-Time PCRTo detect the mRNA level of VEGF-A, platelet-derived growth factor (PDGF)-A, IL-6, proliferating cell nuclear antigen (PCNA), MMP-9, IL-10, IL-12, IFN-a, iNOS and Arg-1 in the lung tissue, the total RNA was extracted following the manufacturer’s protocol (Invitrogen), and 1 mg of total RNA was reverse transcribed using the PrimescriptTM RT reagent kit (TaKaRa, Otsu, Shiga, Japan). Real-time PCR analysis for quantification was performed using a SYBR Premix Ex TaqTM (perfect real time) (TaKaRa). The relative mRNA expression was normalized to GAPDH. The reactions were run in triplicate using the following conditions: one cycle at 95uC for 10 s, subsequently, 40 cycles were performed at 95uC for 5 s and 60uC for 30 s. The median Ct value was determined, and data were expressed as fold change of relative mRNA expression using the comparative Ct method. Primers used are listed in Table S1.Experimental Lung Metastatic ModelIn an experimental metastasis study, two groups of mice (n = 5 in each group) were pretreated with IFN-a or NS for 3 weeks; then all mice were injected with 16106 RFP-LM3 cells via the tail vein. Afterward, both groups received 6 weeks o.Ctive magnification, Olympus).Materials and Methods Animals, Cell Culture, and DrugsSix-week-old male BALB/c nu/nu nude mice weighing approximately 20 g (Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, PR China) were housed in laminar flow cabinets under specific pathogen-free conditions. The mice were cared for in accordance 25033180 with the National Institutes of Health Guidelines for the Care and Use of Laboratory Animals. The experimental protocol was approved by the Shanghai Medical Experimental Animal Care Committee (Approval Number: 2009?556). HCCLM3 human HCC cells [30,31] were grown as a monolayer culture in Dulbecco’s modified Eagle’s medium supplemented with 10 bovine serum albumin. Stable red fluorescent protein (RFP)-expressing HCCLM3 cells[29] were maintained in the same culture as the HCCLM3 cells. All cells were cultured at 37uC in a 5 CO2, 95 air environment in humidified incubators.Orthotopic Nude Mouse ModelThe nude mouse model was established by orthotopic implantation of a histologically intact tumor tissue derived from HCCLM3 or RFP-LM3 cell lines, which had been maintained for more than 80 passages in nude mice. All HCCLM3 and RFPLM3 models exhibited 100 transplantable characteristics and lung metastatic ability as well as various manifestations reminiscent of tumor behavior in patients with HCC. In the first experiment, when the average tumor volume had reached 100 mm3 approximately 1 week after implantation, IFNa (Sinogen, Kexing Bioproduct Company Ltd. Shenzhen, PR China, at a dose of 1.56107 U/kg per injection) or vehicle (normal saline, NS) was injected subcutaneously daily in two groups of mice (n = 6) for 6 weeks. IFN-a withdrawal study was conducted with daily IFN-a treatment for 3 weeks in one group (six mice) followed by daily NS injection for 3 weeks. All mice were sacrificed after 6 weeks of treatment. Tumor size was assessed using the formula: width 6 length 6 depth 6 p/6. Body weights were measured weekly as a surrogate for toxicity. In another animal study using nude mice without tumors, each group of mice (n = 5 in each group) received daily subcutaneous IFN-a or NS injection for 6 weeks, or IFN-a injection for 3 weeks followed by NS injection for another 3 weeks. After 6 weeks of treatment, all mice were sacrificed.Real-Time PCRTo detect the mRNA level of VEGF-A, platelet-derived growth factor (PDGF)-A, IL-6, proliferating cell nuclear antigen (PCNA), MMP-9, IL-10, IL-12, IFN-a, iNOS and Arg-1 in the lung tissue, the total RNA was extracted following the manufacturer’s protocol (Invitrogen), and 1 mg of total RNA was reverse transcribed using the PrimescriptTM RT reagent kit (TaKaRa, Otsu, Shiga, Japan). Real-time PCR analysis for quantification was performed using a SYBR Premix Ex TaqTM (perfect real time) (TaKaRa). The relative mRNA expression was normalized to GAPDH. The reactions were run in triplicate using the following conditions: one cycle at 95uC for 10 s, subsequently, 40 cycles were performed at 95uC for 5 s and 60uC for 30 s. The median Ct value was determined, and data were expressed as fold change of relative mRNA expression using the comparative Ct method. Primers used are listed in Table S1.Experimental Lung Metastatic ModelIn an experimental metastasis study, two groups of mice (n = 5 in each group) were pretreated with IFN-a or NS for 3 weeks; then all mice were injected with 16106 RFP-LM3 cells via the tail vein. Afterward, both groups received 6 weeks o.