Interferon-β is more potent than interferon-α in inhibition of human hepatocellular carcinoma cell growth when used alone and in combination with anticancer drugs

被引:61
作者
Damdinsuren, B [1 ]
Nagano, H [1 ]
Sakon, M [1 ]
Kondo, M [1 ]
Yamamoto, T [1 ]
Umeshita, K [1 ]
Dono, K [1 ]
Nakamori, S [1 ]
Monden, M [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg & Clin Oncol E2, Osaka 5650871, Japan
关键词
interferon; anticancer drug; cell proliferation; HCC; combination therapy;
D O I
10.1245/ASO.2003.03.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The prognosis of advanced hepatocellular carcinoma (HCC) is extremely poor, but promising effects of chemotherapies combined with interferon (IFN) have been reported. Methods: To develop more effective combination therapies for HCC, we compared the antiproliferative effects of IFN-alpha and IFN-beta in combination with various cytotoxic drugs on hepatoma cell lines using MTT assay and isobologram analysis. Results: IFN-beta was more potent than IFN-alpha in inhibiting the cell growth of all cell lines (P <.05, two-way ANOVA). PLC/PRF/5 was more sensitive to either IFN, than HLE and HuH7. Cell growth of all cell lines was inhibited in a dose-dependent manner by 5-fluorouracil (5-FU), cisplatin (CDDP), and doxorubicin (DOX), but the sensitivities of these cells were considerably different. As for IFN-α, synergistic effects were observed when combined with 5-FU and DOX on PLC/PRF/5 cells only, whereas IFN-β showed synergistic effects with 5-FU and CDDP on HuH7 and PLC/ PRF/5 cell lines. Conclusion: The spectra of the antiproliferative activity and synergistic effect of IFN-β when combined with anticancer drugs are more potent than those of IFN-α. Combinations of IFN-β and anticancer drugs may provide a better treatment of HCC when combinations with IFN-α are ineffective.
引用
收藏
页码:1184 / 1190
页数:7
相关论文
共 26 条
[1]   Hepatocellular carcinoma: an overview [J].
Anthony, PP .
HISTOPATHOLOGY, 2001, 39 (02) :109-118
[2]   CRITERIA FOR ANALYZING INTERACTIONS BETWEEN BIOLOGICALLY-ACTIVE AGENTS [J].
BERENBAUM, MC .
ADVANCES IN CANCER RESEARCH, 1981, 35 :269-335
[3]   Epidemiology of primary liver cancer [J].
Bosch, FX ;
Ribes, J ;
Borràs, J .
SEMINARS IN LIVER DISEASE, 1999, 19 (03) :271-285
[4]  
Chawla-Sarkar M, 2001, CLIN CANCER RES, V7, P1821
[5]  
CORADINI D, 1994, ANTICANCER RES, V14, P1779
[6]  
Eguchi H, 2000, CLIN CANCER RES, V6, P2881
[7]  
Giandomenico V, 1998, EUR CYTOKINE NETW, V9, P619
[8]  
Horikoshi Takashi, 1995, Journal of Dermatology (Tokyo), V22, P631
[9]   Hepatocellular carcinoma: is current therapy really altering outcome? [J].
Johnson, PJ .
GUT, 2002, 51 (04) :459-462
[10]   Interferon in oncological practice: Review of interferon biology, clinical applications, and toxicities [J].
Jonasch, E ;
Haluska, FG .
ONCOLOGIST, 2001, 6 (01) :34-55