Osteosarcoma and chondrosarcoma as targets for virus vectors and herpes simplex virus thymidine kinase/ganciclovir gene therapy

被引:10
作者
Ketola, A
Määttä, AM
Pasanen, T
Tulimäki, K
Wahlfors, J
机构
[1] Univ Kuopio, AI Virtanen Inst Mol Sci, Dept Biotechnol & Mol Med, FIN-70211 Kuopio, Finland
[2] Kuopio Univ Hosp, Gene Therapy Unit, SF-70210 Kuopio, Finland
关键词
adenovirus; chondrosarcoma; fusion gene; gene therapy; green fluorescent protein; osteosarcoma; thymidine kinase;
D O I
暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Osteosarcoma and chondrosarcoma, the most prevalent primary malignant tumors of the bone, have been demonstrated to be potential target diseases for herpes simplex virus type 1 thymidine kinase (HSV-TK)/ganciclovir (GCV) suicide gene therapy. However, the utility of this gene therapy form for bone tumor cells has not been studied systematically. In this report we show, with the aid of three osteosarcoma cell lines (Saos-2, U-2-OS and MG-63) and one chondrosarcoma cell line (SW1353) that: i) these tumor cells were permissive for adenovirus- or lentivirus-mediated gene delivery; ii) the cell lines appeared to be good or excellent targets for HSV-TK/GCV gene therapy; and iii) the extent of HSV-TK/GCV cytotoxic effect correlated with the presence of the 'bystander effect' in these cells. Our results also suggest that lentiviruses are potential vectors for bone cancer gene therapy. They transduced all four cell lines with high efficiency and provided HSV-TK expression level that was sufficient for cytotoxicity and bystander effect comparable to that obtained with adenovirus vectors.
引用
收藏
页码:705 / 710
页数:6
相关论文
共 18 条
[1]  
Charissoux JL, 1999, ANTICANCER RES, V19, P77
[2]   INVIVO GENE-TRANSFER WITH RETROVIRAL VECTOR PRODUCER CELLS FOR TREATMENT OF EXPERIMENTAL BRAIN-TUMORS [J].
CULVER, KW ;
RAM, Z ;
WALLBRIDGE, S ;
ISHII, H ;
OLDFIELD, EH ;
BLAESE, RM .
SCIENCE, 1992, 256 (5063) :1550-1552
[3]  
Gomes A., 2000, GENE THER MOL BIOL, V5, P165
[4]  
Grossin L, 1999, ANTICANCER RES, V19, P71
[5]  
Ko SC, 1996, CANCER RES, V56, P4614
[6]   Human prostate carcinoma cells as targets for herpes simplex virus thymidine kinase-mediated suicide gene therapy [J].
Loimas, S ;
Toppinen, MR ;
Visakorpi, T ;
Jänne, J ;
Wahlfors, J .
CANCER GENE THERAPY, 2001, 8 (02) :137-144
[7]   Herpes simplex virus thymidine kinase green fluorescent protein fusion gene:: New tool for gene transfer studies and gene therapy [J].
Loimas, S ;
Wahlfors, J ;
Jänne, J .
BIOTECHNIQUES, 1998, 24 (04) :614-618
[8]   Experience in the treatment of dedifferentiated chondrosarcoma [J].
Mitchell, AD ;
Ayoub, K ;
Mangham, DC ;
Grimer, RJ ;
Carter, SR ;
Tillman, RM .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 2000, 82B (01) :55-61
[9]  
MOOLTEN FL, 1986, CANCER RES, V46, P5276
[10]   In vivo gene delivery and stable transduction of nondividing cells by a lentiviral vector [J].
Naldini, L ;
Blomer, U ;
Gallay, P ;
Ory, D ;
Mulligan, R ;
Gage, FH ;
Verma, IM ;
Trono, D .
SCIENCE, 1996, 272 (5259) :263-267