Inhibitory effect of interferon-α-2b on expression of cyclooxygenase-2 and vascular endothelial growth factor in human hepatocellular carcinoma inoculated in nude mice
AIM:To evaluate the effects of interferon-α-2b (IFN-α-2b) on expression of cyclooxygenase-2 (COX-2) and vascular endothelial growth factor (VEGF) in human hepatocellular carcinoma (HCC) inoculated in nude mice and to study the underlying mechanism of IFN-α-2b against HCC growth. METHODS:Thirty-two nude mice bearing human HCC were randomly divided into four groups (n = 8). On the 10th day after implantation of HCC cells,the mice in test groups (groups A,B and C) received IFN-α-2b at a serial dose (10 000 IU for group A,20 000 IU for group B,40 000 IU for group C sc daily) for 35 d. The mice in control group received normal saline (NS). The growth conditions of transplanted tumors were observed. Both genes and proteins of COX-2 and VEGF were detected by RT-PCR and Western blot. Apoptosis of tumor cells in nude mice was detected by TUNEL assay after treatment with IFN-α-2b. RESULTS:Tumors were significantly smaller and had a lower weight in the IFN-α-2b treatment groups than those in the control group (P < 0.01),and the tumor growth inhibition rate in groups A,B and C was 27.78%,65.22% and 49.64%,respectively. The expression levels of both genes and proteins of COX-2 and VEGF were much lower in the IFN-α-2b treatment groups than in the control group (P < 0.01). The apoptosis index (AI) of tumor cells in the IFN-α-2b treatment groups was markedly higher than that in the control group (P < 0.01). Group B had a higher inhibition rate of tumor growth,a lower expression level of COX-2 and VEGF and a higher AI than groups A and C (P < 0.05),but there was no significant difference between groups A and C. CONCLUSION:The inhibitory effects of IFN-α-2b on implanted tumor growth and apoptosis may be associated with the down-regulation of COX-2 and VEGF expression. There is a dose-effect relationship. The medium dose of IFN-α-2b for inhibiting tumor growth is 20 000 IU/d.
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Capital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R ChinaCapital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R China
Zhi, Ying-Hui
Liu, Ruo-Shan
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Second Mil Med Univ, Changhai Hosp, Dept Anesthesiol, Shanghai 200433, Peoples R ChinaCapital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R China
Liu, Ruo-Shan
Song, Mao-Min
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Capital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R ChinaCapital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R China
Song, Mao-Min
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Tian, Yu
Long, Jin
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China Med Univ, Affiliated Hosp 1, Dept Gen Surg 2, Shenyang 110001, Liaoning Provin, Peoples R ChinaCapital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R China
Long, Jin
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Tu, Wei
Guo, Ren-Xuan
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China Med Univ, Affiliated Hosp 1, Dept Gen Surg 2, Shenyang 110001, Liaoning Provin, Peoples R ChinaCapital Univ Med Sci, Affiliated Beijing Tiantan Hosp, Dept Gen Surg, Beijing 100050, Peoples R China
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Hong Kong, Hong Kong, Peoples R China
Hong Kong Polytech Univ, State Key Lab Chinese Med & Mol Pharmacol, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
Pak, K. C.
Lam, K. Y.
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Griffith Univ, Griffith Med Sch, Nathan, Qld 4111, AustraliaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
Lam, K. Y.
Law, S.
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Univ Hong Kong, Dept Surg, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
Law, S.
Tang, J. C. O.
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Hong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China
Hong Kong Polytech Univ, Lo Ka Chung Ctr Nat Anticanc Drug Dev, Hong Kong, Hong Kong, Peoples R China
Hong Kong Polytech Univ, State Key Lab Chinese Med & Mol Pharmacol, Hong Kong, Hong Kong, Peoples R ChinaHong Kong Polytech Univ, Dept Appl Biol & Chem Technol, Hong Kong, Hong Kong, Peoples R China