The use of a genetically engineered herpes simplex virus (R7020) with ionizing radiation for experimental hepatoma

被引:48
作者
Chung, SM
Advani, SJ
Bradley, JD
Kataoka, Y
Vashistha, K
Yan, SY
Markert, JM
Gillespie, GY
Whitley, RJ
Roizman, B
Weichselbaum, RR
机构
[1] Univ Chicago Hosp, Dept Radiat & Cellular Oncol, Pritzker Sch Med, Chicago, IL 60637 USA
[2] Univ Alabama Birmingham, Dept Pediat Microbiol & Med, Birmingham, AL USA
[3] Univ Alabama Birmingham, Dept Surg, Div Neurosurg, Brain Tumor Res Labs, Birmingham, AL USA
[4] Univ Chicago, Marjorie B Kovler Viral Oncol Labs, Chicago, IL 60637 USA
关键词
HSV; gene therapy;
D O I
10.1038/sj.gt.3301620
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The herpes simplex virus (HSV) recombinant virus R7020 is an attenuated virus designed as a candidate for immunization against both HSV-1 and HSV-2 infections. It was extensively tested in an experimental animal system and in a healthy human adult population without significant untoward effects. We report on the use of R7020 with ionizing radiation as an oncolytic agent for hepatomas. Two hepatoma cell lines were studied, Hep3B and Huh7. R7020 replicated to higher titers in Hep3B cells than in Huh7 cells. Tissue culture studies correlated with hepatoma xenograft responses to R7020. R7020 was more effective in mediating Hep3B tumor xenograft regression compared with Huh7. Ionizing radiation combined with R7020 also showed differential results in antitumor efficacy between the two cell lines in tumor xenografts. Ionizing radiation enhanced the replication of R7020 in Hep3B xenografts. Moreover, the combination of ionizing radiation and virus caused a greater regression of xenograft volume than either R7020 or radiation alone. Ionizing radiation had no effect on the replication of R7020 virus in Huh7 xenografts. These results indicate that a regimen involving infection with an appropriate herpesvirus such as R7020 in combination with ionizing radiation can be highly effective in eradicating certain tumor xenografts.
引用
收藏
页码:75 / 80
页数:6
相关论文
共 29 条
[1]  
Advani SJ, 1997, SEMIN ONCOL, V24, P633
[2]  
Advani SJ, 1999, CANCER RES, V59, P2055
[3]   Enhancement of replication of genetically engineered herpes simplex viruses by ionizing radiation: a new paradigm for destruction of therapeutically intractable tumors [J].
Advani, SJ ;
Sibley, GS ;
Song, PY ;
Hallahan, DE ;
Kataoka, Y ;
Roizman, B ;
Weichselbaum, RR .
GENE THERAPY, 1998, 5 (02) :160-165
[4]  
Andreansky S, 1997, CANCER RES, V57, P1502
[5]   An adenovirus mutant that replicates selectively in p53-deficient human tumor cells [J].
Bischoff, JR ;
Kim, DH ;
Williams, A ;
Heise, C ;
Horn, S ;
Muna, M ;
Ng, L ;
Nye, JA ;
SampsonJohannes, A ;
Fattaey, A ;
McCormick, F .
SCIENCE, 1996, 274 (5286) :373-376
[6]  
Bradley JD, 1999, CLIN CANCER RES, V5, P1517
[7]   Selective infection and cytolysis of human head and neck squamous cell carcinoma with sparing of normal mucosa by a cytotoxic herpes simplex virus type 1 (G207) [J].
Carew, JF ;
Kooby, DA ;
Halterman, MW ;
Federoff, HJ ;
Fong, YM .
HUMAN GENE THERAPY, 1999, 10 (10) :1599-1606
[8]  
Chahlavi Ali, 1999, Neoplasia (New York), V1, P162, DOI 10.1038/sj.neo.7900016
[9]   COMPARISON OF GENETICALLY-ENGINEERED HERPES-SIMPLEX VIRUSES FOR THE TREATMENT OF BRAIN-TUMORS IN A SCID MOUSE MODEL OF HUMAN-MALIGNANT GLIOMA [J].
CHAMBERS, R ;
GILLESPIE, GY ;
SOROCEANU, L ;
ANDREANSKY, S ;
CHATTERJEE, S ;
CHOU, J ;
ROIZMAN, B ;
WHITLEY, RJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (05) :1411-1415
[10]   MAPPING OF HERPES-SIMPLEX VIRUS-1 NEUROVIRULENCE TO GAMMA-134.5, A GENE NONESSENTIAL FOR GROWTH IN CULTURE [J].
CHOU, J ;
KERN, ER ;
WHITLEY, RJ ;
ROIZMAN, B .
SCIENCE, 1990, 250 (4985) :1262-1266