Cancer gene therapy: Scientific basis

被引:45
作者
Wadhwa, PD [1 ]
Zielske, SP
Roth, JC
Ballas, CB
Bowman, JE
Gerson, SL
机构
[1] Univ Hosp Cleveland, Div Hematol Oncol, Cleveland, OH 44106 USA
[2] Univ Hosp Cleveland, Ctr Comprehens Canc, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Cleveland, OH 44106 USA
来源
ANNUAL REVIEW OF MEDICINE | 2002年 / 53卷
关键词
tumor suppressor genes; suicide genes; dendritic cells; angiogenesis; chemotherapy-resistance genes;
D O I
10.1146/annurev.med.53.082901.104039
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
Gene therapy of cancer has been one of the most exciting and elusive areas of therapeutic research in the past decade. Critical developments have occurred in gene therapy targeting cancer cells, cancer vasculature, the immune system, and the bone marrow, itself often the target for severe toxicity from therapeutic agents. We review some recent developments in the field. In each instance, clear preclinical models validated the therapeutic approach and efforts have been made to evaluate the target impact in both preclinical and early clinical trials. Although no cures can consistently be expected from today's cancer gene therapy, the rapid progress may imply that such cures are a few short years away.
引用
收藏
页码:437 / 452
页数:16
相关论文
共 88 条
[1]   Efficient retrovirus-mediated transfer of the multidrug resistance 1 gene into autologous human long-term repopulating hematopoietic stem cells [J].
Abonour, R ;
Williams, DA ;
Einhorn, L ;
Hall, KM ;
Chen, J ;
Coffman, J ;
Traycoff, CM ;
Bank, A ;
Kato, I ;
Ward, M ;
Williams, SD ;
Hromas, R ;
Robertson, MJ ;
Smith, FO ;
Woo, D ;
Mills, B ;
Srour, EF ;
Cornetta, K .
NATURE MEDICINE, 2000, 6 (06) :652-658
[2]   In vivo selection of retrovirally transduced hematopoietic stem cells [J].
Allay, JA ;
Persons, DA ;
Galipeau, J ;
Riberdy, JM ;
Ashmun, RA ;
Blakley, RL ;
Sorrentino, BP .
NATURE MEDICINE, 1998, 4 (10) :1136-1143
[3]   Coexpression of cytidine deaminase and mutant dihydrofolate reductase by a bicistronic retroviral vector confers resistance to cytosine arabinoside and methotrexate [J].
Beauséjour, CM ;
Le, NLO ;
Létourneau, S ;
Cournoyer, D ;
Momparler, RL .
HUMAN GENE THERAPY, 1998, 9 (17) :2537-2544
[4]   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
[5]   Creation of drug-specific herpes simplex virus type 1 thymidine kinase mutants for gene therapy [J].
Black, ME ;
Newcomb, TG ;
Wilson, HMP ;
Loeb, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) :3525-3529
[6]   Gene therapy of metastatic colon carcinoma: Regression of multiple hepatic metastases by adenoviral expression of bacterial cytosine deaminase [J].
Block, A ;
Freund, CTF ;
Chen, SH ;
Nguyen, KP ;
Finegold, M ;
Windler, E ;
Woo, SLC .
CANCER GENE THERAPY, 2000, 7 (03) :438-445
[7]  
BRENT TP, 1987, CANCER RES, V47, P6185
[8]   Adoptive tumor immunity mediated by lymphocytes bearing modified antigen-specific receptors [J].
Brocker, T ;
Karjalainen, K .
ADVANCES IN IMMUNOLOGY, VOL 68, 1998, 68 :257-269
[9]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[10]   Immunogenetic therapy of human melanoma utilizing autologous tumor cells transduced to secrete granulocyte-macrophage colony-stimulating factor [J].
Chang, AE ;
Li, Q ;
Bishop, DK ;
Normolle, DP ;
Redman, BD ;
Nickoloff, BJ .
HUMAN GENE THERAPY, 2000, 11 (06) :839-850