Gene therapy and virotherapy of gastric cancer: Preclinical results and clinical developments

被引:2
作者
Heideman, DAM [1 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Pathol, NL-1007 MB Amsterdam, Netherlands
关键词
gene transfer; viral vector; oncolytic virus; gastric cancer; stomach cancer; gastrointestinal cancer;
D O I
10.1159/000083601
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Despite advances in current treatment modalities, the clinical outcome of gastric cancer remains dismal. New treatment modalities are urgently required to improve the prognosis of patients with gastric cancer. Cancer gene therapy and virotherapy comprise a potential category of new therapeutics and will be discussed in this review. To date, various gene therapy strategies have been developed, but first clinical trials reported only limited therapeutic efficacy as a result of limited gene transfer efficiency. Consequently, targeted viral vectors for enhanced delivery of transgenes to tumor cells and replicative viral systems designed to replicate selectively in malignant tissue were developed. Replication-selective oncolytic viral vectors have the advantage over non-replicative systems to cause pronounced bystander effect via self-perpetuating infection of adjacent cells after cytolysis of primary targeted cells. So far, clinical studies on virotherapy showed encouraging results; especially promising are combinations of virotherapy with current modes of treatment like chemo- and radiotherapy, or insertion of therapeutic genes in the viral genome such as combination with enzyme-prodrug therapy. Further research aiming to enhance anti-tumor efficacy and to improve selectivity of infection and replication, will eventually lead to full realization of the therapeutic potential of ( replicating) viral vector systems for gastric cancer. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:374 / 379
页数:6
相关论文
共 50 条
[31]   Newcastle disease virus therapy of human tumor xenografts: antitumor effects of local or systemic administration [J].
Phuangsab, A ;
Lorence, RM ;
Reichard, KW ;
Peeples, ME ;
Walter, RJ .
CANCER LETTERS, 2001, 172 (01) :27-36
[32]   Parvovirus vectors for cancer gene therapy [J].
Ponnazhagan, S .
EXPERT OPINION ON BIOLOGICAL THERAPY, 2004, 4 (01) :53-64
[33]  
Reid T, 2002, CANCER RES, V62, P6070
[34]  
Rodriguez R, 1997, CANCER RES, V57, P2559
[35]   Gene therapy for cancer: What have we done and where are we going? [J].
Roth, JA ;
Cristiano, RJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1997, 89 (01) :21-39
[36]  
Schirrmacher V, 2001, INT J ONCOL, V18, P945
[37]   Prodrug-activating systems in suicide gene therapy [J].
Springer, CJ ;
Niculescu-Duvaz, I .
JOURNAL OF CLINICAL INVESTIGATION, 2000, 105 (09) :1161-1167
[38]   Exploiting tumor-specific defects in the interferon pathway with a previously unknown oncolytic virus [J].
Stojdl, DF ;
Lichty, B ;
Knowles, S ;
Marius, R ;
Atkins, H ;
Sonenberg, N ;
Bell, JC .
NATURE MEDICINE, 2000, 6 (07) :821-825
[39]   The molecular basis of viral oncolysis: usurpation of the Ras signaling pathway by reovirus [J].
Strong, JE ;
Coffey, MC ;
Tang, D ;
Sabinin, P ;
Lee, PWK .
EMBO JOURNAL, 1998, 17 (12) :3351-3362
[40]   E1B-55K-deleted adenovirus expressing E1A-13S by AFP-enhancer/promoter is capable of highly specific replication in AFP-producing hepatocellular carcinoma and eradication of established tumor [J].
Takahashi, M ;
Sato, T ;
Sagawa, T ;
Lu, Y ;
Sato, Y ;
Iyama, S ;
Yamada, Y ;
Fukaura, J ;
Takahashi, S ;
Miyanishi, K ;
Yamashita, T ;
Sasaki, K ;
Kogawa, K ;
Hamada, H ;
Kato, J ;
Niitsu, Y .
MOLECULAR THERAPY, 2002, 5 (05) :627-634