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.
引用
收藏
页码:493 / 499
页数:7
相关论文
共 21 条
[1]   Gene transfer into muscle by electroporation in vivo [J].
Aihara, H ;
Miyazaki, J .
NATURE BIOTECHNOLOGY, 1998, 16 (09) :867-870
[2]  
CHEN SH, 1992, CANCER RES, V52, P1329
[3]   Distribution of DNA vaccines determines their immunogenicity after intramuscular injection in mice [J].
Dupuis, M ;
Denis-Mize, K ;
Woo, C ;
Goldbeck, C ;
Selby, MJ ;
Chen, MC ;
Otten, GR ;
Ulmer, JB ;
Donnelly, JJ ;
Ott, G ;
McDonald, DM .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2850-2858
[4]   Down-regulated melanoma differentiation associated gene (MDA-7) expression in human melanomas [J].
Ekmekcioglu, S ;
Ellerhorst, J ;
Mhashilkar, AM ;
Sahin, AA ;
Read, CM ;
Prieto, VG ;
Chada, S ;
Grimm, EA .
INTERNATIONAL JOURNAL OF CANCER, 2001, 94 (01) :54-59
[5]   Loss of MDA-7 expression with progression of melanoma [J].
Ellerhorst, JA ;
Prieto, VG ;
Ekmekcioglu, S ;
Broemeling, L ;
Yekell, S ;
Chada, S ;
Grimm, EA .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (04) :1069-1074
[6]   A gene therapy for cancer using intramuscular injection of plasmid DNA encoding interferon α [J].
Horton, HM ;
Anderson, D ;
Hernandez, P ;
Barnhart, KM ;
Norman, JA ;
Parker, SE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (04) :1553-1558
[7]   Genomic structure, chromosomal localization and expression profile of a novel melanoma differentiation associated (mda-7) gene with cancer specific growth suppressing and apoptosis inducing properties [J].
Huang, EY ;
Madireddi, MT ;
Gopalkrishnan, RV ;
Leszczyniecka, M ;
Su, ZZ ;
Lebedeva, IV ;
Kang, DC ;
Jiang, HP ;
Lin, JJ ;
Alexandre, D ;
Chen, YM ;
Vozhilla, N ;
Mei, MX ;
Christiansen, KA ;
Sivo, F ;
Goldstein, NI ;
Mhashilkar, AB ;
Chada, S ;
Huberman, E ;
Pestka, S ;
Fisher, PB .
ONCOGENE, 2001, 20 (48) :7051-7063
[8]  
Jiang HP, 1995, ONCOGENE, V11, P2477
[9]   Antitumor applications of stimulating Toll-like receptor 9 with CpG oligodeoxynucleotides [J].
Krieg A.M. .
Current Oncology Reports, 2004, 6 (2) :88-95
[10]   Inhibition of established subcutaneous and metastatic murine tumors by intramuscular electroporation of the interleukin-12 gene [J].
Lee, SC ;
Wu, CJ ;
Wu, PY ;
Huang, YL ;
Wu, CW ;
Tao, MH .
JOURNAL OF BIOMEDICAL SCIENCE, 2003, 10 (01) :73-86