IL-24 inhibits the growth of hepatoma cells in vivo

被引:37
|
作者
Chen, WY
Cheng, YT
Lei, HY
Chang, CP
Wang, CW
Chang, MS [1 ]
机构
[1] Natl Cheng Kung Univ, Coll Med, Grad Inst Biochem & Mol Biol, Tainan 704, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Grad Inst Microbiol & Immunol, Tainan, Taiwan
[3] Chi Mei Med Ctr, Tainan, Taiwan
[4] Natl Cheng Kung Univ, Coll Med, Inst Basic Med Sci, Tainan 70101, Taiwan
关键词
IL-24; mda-7; hepatoma; intramuscular electroporation;
D O I
10.1038/sj.gene.6364233
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The interleukin (IL)-24/melanoma differentiation associated gene-7 (mda-7) is a member of the IL-10 cytokine family. Introduction of the IL-24 gene into a variety of cancer cells suppresses their growth. It has not been shown, however, whether IL-24 can suppress the growth of hepatoma cells. The purpose of this study was to determine whether the mouse (m)IL-24 gene would suppress hepatoma cells in vivo after being delivered via intramuscular electroporation. After mice were given a subcutaneous dorsal injection of ML-1 hepatoma cells, the mIL-24 gene was delivered and suppressed tumor growth. On day 140, 60% of the mIL-24-treated mice (n = 10) and 0% (n = 10) of the untreated control mice had survived. We also generated a mouse-hepatoma model by injecting ML-1 cells into the spleen, which resulted in tumor metastasis in the liver. Intramuscular electroporation of mIL-24 also inhibited hepatoma-cell growth in the liver. On day 50, 90% of the experimental mice (n = 10) and 40% (n = 10) of the control mice had survived. Liver tumors in surviving experimental mice were 50% smaller than those in control mice. IL-24 also inhibited tumor vascularization. These results suggest that IL-24 has potential therapeutic value for hepatoma.
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页码:493 / 499
页数:7
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