Adenoviral interleukin-3 gene-radiation therapy for prostate cancer in mouse model

被引:18
作者
Oh, YT
Chen, DWC
Dougherty, GJ
McBride, WH
机构
[1] Ajou Univ, Sch Med, Dept Radiat Oncol, Suwon 442721, South Korea
[2] Chang Gung Mem Hosp, Dept Radiat Oncol, Chiayi, Taiwan
[3] Univ Calif Los Angeles, Sch Med, Dept Radiat Oncol, Expt Div, Los Angeles, CA USA
来源
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS | 2004年 / 59卷 / 02期
关键词
interleukin-3; gene therapy; radiation therapy; prostate cancer; adenovirus;
D O I
10.1016/j.ijrobp.2004.01.030
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose: The radiosensitizing effect of IL-3 gene therapy was evaluated on the syngeneic mouse prostate cancer model. Methods and Materials: An adenoviral vector was used to deliver the mIL-3 alpha gene into syngeneic murine prostate (TRAMP-Cl) cancer cells growing in a subcutaneous site and the tumor response to irradiation was assessed. Results: Ad-mIL-3 gene therapy showed no tumor growth delay without radiation. However, intratumoral Ad-mIL-3 injection with radiation therapy showed marked tumor growth delay that was significantly greater than that of radiation alone. Conclusions: The combined intratumoral Ad-mIL-3 gene therapy and radiation therapy is a valuable option for further clinical evaluation. (C) 2004 Elsevier Inc.
引用
收藏
页码:579 / 583
页数:5
相关论文
共 26 条
[1]   Enhanced antitumor effects of bone marrow transplantation in combination with fibroblast-mediated IL-2 and IL-3 gene therapy [J].
Cao, XT ;
Li, Q ;
Ju, DW ;
Wang, QX ;
Tao, Q ;
Wang, JL .
TRANSPLANTATION, 1999, 67 (09) :1242-1250
[2]   Interleukin-3 cooperates with tumor necrosis factor alpha for the development of human dendritic Langerhans cells from cord blood CD34(+) hematopoietic progenitor cells [J].
Caux, C ;
Vanbervliet, B ;
Massacrier, C ;
Durand, I ;
Banchereau, J .
BLOOD, 1996, 87 (06) :2376-2385
[3]  
Chiang CS, 1997, CANCER RES, V57, P3899
[4]   Combining radiation therapy with interleukin-3 gene immunotherapy [J].
Chiang, CS ;
Hong, JH ;
Wu, YC ;
McBride, WH ;
Dougherty, GJ .
CANCER GENE THERAPY, 2000, 7 (08) :1172-1178
[5]   Gene therapy: The challenges of translating laboratory research into clinical practice [J].
Connell, PP ;
Weichselbaum, RR .
JOURNAL OF CLINICAL ONCOLOGY, 2003, 21 (12) :2230-2231
[6]  
Croyle M A, 1998, Pharm Dev Technol, V3, P365, DOI 10.3109/10837459809009864
[7]   IL-3 in the clinic [J].
Eder, M ;
Geissler, G ;
Ganser, A .
STEM CELLS, 1997, 15 (05) :327-333
[8]   Prostate cancer gene therapy [J].
Ferrer, FA ;
Rodriguez, R .
HEMATOLOGY-ONCOLOGY CLINICS OF NORTH AMERICA, 2001, 15 (03) :497-+
[9]   Efficacy and toxicity of replication-competent adenovirus-mediated double suicide gene therapy in combination with radiation therapy in an orthotopic mouse prostate cancer model [J].
Freytag, SO ;
Paielli, D ;
Wing, M ;
Rogulski, K ;
Brown, S ;
Kolozsvary, A ;
Seely, J ;
Barton, K ;
Dragovic, A ;
Kim, JH .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 2002, 54 (03) :873-885
[10]   Cancer gene therapy clinical trials: lessons for the future [J].
Galanis, E ;
Russell, S .
BRITISH JOURNAL OF CANCER, 2001, 85 (10) :1432-1436