Effective treatment of experimental glioblastoma by HSV vector-mediated TNFα and HSV-tk gene transfer in combination with radiosurgery and ganciclovir administration

被引:70
|
作者
Niranjan, A
Moriuchi, S
Lunsford, LD
Kondziolka, D
Flickinger, JC
Fellows, W
Rajendiran, S
Tamura, M
Cohen, JB
Glorioso, JC
机构
[1] Univ Pittsburgh, Sch Med, Dept Mol Genet & Biochem, Pittsburgh, PA 15261 USA
[2] Univ Pittsburgh, Sch Med, Dept Neurol Surg, Pittsburgh, PA 15261 USA
[3] Univ Pittsburgh, Sch Med, Dept Radiat Oncol, Pittsburgh, PA 15261 USA
[4] Univ Pittsburgh, Sch Med, Dept Radiol, Pittsburgh, PA 15261 USA
[5] Univ Pittsburgh, Sch Med, Dept Pathol, Pittsburgh, PA 15261 USA
关键词
D O I
10.1006/mthe.2000.0101
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Experiments were carried out in a nude mouse model of human glioblastoma to determine whether gamma-knife radiosurgery combined with herpes simplex virus thymidine kinase (tk) suicide gene therapy and tumor necrosis factor alpha (TNF alpha) gene transfer provided an improved multimodality treatment of this disease. Animals were inoculated intracerebrally with 2 X 10(5) U-87MG human glioblastoma cells to establish brain tumors. At 3 days postinoculation, the tumor region was injected with 2 x 10(6) infectious particles of highly defective herpes simplex viral vectors expressing the viral tk gene with the kinetics of a viral immediate early gene either alone (T.1) or together with TNF alpha (TH:TNF). Subgroups of animals were given dairy intraperitoneal injections of ganciclovir (GCV) for 10 days and/or subjected to gamma-knife radiosurgery on the fifth day post tumor-cell implantation. Comparisons of animal survival showed that the TH:TNF vector in combination with radiosurgery and GCV administration provided the most effective therapy; eight of nine animals survived for 75 days compared to four of eight using the next best protocol. These findings suggest that gene therapy in combination with more conventional therapeutic methods may provide an improved strategy for extending the life expectancy of patients afflicted with this ultimately fatal disease.
引用
收藏
页码:114 / 120
页数:7
相关论文
共 50 条
  • [1] In vivo transduction with retroviral vector bearing HSV-tk gene followed by ganciclovir treatment in experimental proliferative vitreoretinopathy
    Kimura, H
    Cardillo, JA
    Spee, C
    Hinton, DR
    Gordon, EM
    Anderson, WF
    Ryan, SJ
    INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 1996, 37 (03) : 1815 - 1815
  • [2] TUMOR-SPECIFIC CTLS INDUCED BY HSV-TK GENE-TRANSFER AND GANCICLOVIR TREATMENT
    SUZUKI, S
    SHIMIZU, H
    HOSHINO, A
    YAMAMOTO, S
    IGARASHI, T
    SHIMADA, T
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, : 427 - 427
  • [3] TREATMENT OF HEPATOCELLULAR-CARCINOMA THROUGH ADENOVIRUS-MEDIATED GENE-TRANSFER OF THE HSV-TK GENE IN COMBINATION WITH THE NUCLEOSIDE ANALOG DRUG GANCICLOVIR
    WILLS, KN
    HARRIS, MP
    HUANG, WM
    MACHEMER, T
    MANEVAL, DC
    GREGORY, RJ
    JOURNAL OF CELLULAR BIOCHEMISTRY, 1995, : 429 - 429
  • [4] Differential response of glial cell lines to adenovirus-mediated gene transfer of HSV-TK and ganciclovir administration in vitro and in vivo
    Shine, HD
    Barth, RF
    JOURNAL OF NEUROCHEMISTRY, 1996, 66 : S68 - S68
  • [5] Suppression of Bladder Cancer Growth by Adeno-associated Virus Vector-mediated Combination of HSV-TK and Endostatin In Vitro
    Pan, Jian Gang
    Luo, Run Qi
    Zhou, Xing
    Han, Rui Fa
    Zeng, Ge Wa
    CLINICAL LABORATORY, 2013, 59 (9-10) : 1077 - 1089
  • [6] Enhanced killing of glioblastoma cells by HSV-1 vector mediated combined IκBα mutant and HSV-TK expression under GCV administration
    Moriuchi, S
    Yamasaki, M
    Yoshimine, T
    Wolf, D
    Huang, SH
    Cohen, J
    Glorioso, JC
    MOLECULAR THERAPY, 2003, 7 (05) : S286 - S287
  • [7] Combination gene therapy with adenoviral vector-mediated HSV-tk plus GCV and IL-12 in an orthotopic mouse model for prostate cancer
    Nasu, Y
    Bangma, CH
    Hull, GW
    Yang, G
    Wang, J
    Shimura, S
    McCurdy, MA
    Ebara, S
    Lee, HM
    Timme, TL
    Thompson, TC
    PROSTATE CANCER AND PROSTATIC DISEASES, 2001, 4 (01) : 44 - 55
  • [8] Adenovirus-mediated HSV-tk/ganciclovir gene therapy in a mammary cancer transgenic mouse model
    RojasMartinez, A
    Donehower, L
    Montgomery, C
    AguilarCordova, E
    CANCER GENE THERAPY, 1997, 4 (06) : P118 - P118
  • [9] Effects of HSV-TK and IL-4 gene transfer in experimental gliomas.
    Benedetti, S
    DiMeco, F
    Cirenei, N
    Pollo, B
    Bruzzone, MG
    Colombo, BM
    Vescovi, A
    Colombo, M
    DiDonato, S
    Finocchiaro, G
    CANCER GENE THERAPY, 1996, 3 (06) : P91 - P91
  • [10] Gene therapy of HSV-TK transferred by the EBV based expression vector on experimental hepatocellular carcinoma
    Ding, Q.
    Wu, Z.
    Chen, X.
    Musa, A.H.M.
    Hu, J.
    Zhan, Y.
    Journal of Tongji Medical University, 2001, 21 (02) : 122 - 125