MOLECULAR APPROACHES TO CANCER-THERAPY

被引:11
作者
ISRAEL, MA
机构
[1] University of California at San Francisco, San Francisco
来源
ADVANCES IN CANCER RESEARCH, VOL 61 | 1993年 / 61卷
关键词
D O I
10.1016/S0065-230X(08)60955-0
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This chapter discusses the proposed molecular approaches to cancer therapy. Cancer arises as a series of molecular alterations that converge to give the cell malignant properties. The genes closely associated with the development of cancer encode products whose activities are easily reconciled with the malignant phenotype of cancer cells. The ability to characterize tumors at the molecular level and to use modern biological and chemical technologies to identify and develop novel molecules of therapeutic potential has opened several possible avenues for the development of new therapeutic modalities. The molecular approaches used are novel antineoplastic agents, modern immunotherapy, and the therapeutic repair of oncogenic genetic lesions. Most antineoplastic agents interact with DNA in a manner that inhibits the replication of the tumor cell genome. Modern immunotherapy for cancer or biologic therapy has both active and passive approaches. Drugs that target specific molecules and gene therapy are divergent approaches to the treatment of cancer. Gene therapy involves the introduction of new genetic information into cells. Gene therapy offers the possibility for novel approaches to the development of tumor vaccines. © 1993, Academic Press Inc.
引用
收藏
页码:57 / 85
页数:29
相关论文
共 139 条
[1]  
Abdel-Nabi H, 1992, Semin Urol, V10, P45
[2]  
AKIYAMA T, 1987, J BIOL CHEM, V262, P5592
[3]   ADOPTIVELY TRANSFERRED TUMOR-INFILTRATING LYMPHOCYTES CAN CURE ESTABLISHED METASTATIC TUMOR IN MICE AND PERSIST LONG-TERM INVIVO AS FUNCTIONAL MEMORY LYMPHOCYTES-T [J].
ALEXANDER, RB ;
ROSENBERG, SA .
JOURNAL OF IMMUNOTHERAPY, 1991, 10 (06) :389-397
[4]   INTERFERON-GAMMA AND TUMOR-NECROSIS-FACTOR HAVE A ROLE IN TUMOR REGRESSIONS MEDIATED BY MURINE CD8+ TUMOR-INFILTRATING LYMPHOCYTES [J].
BARTH, RJ ;
MULE, JJ ;
SPIESS, PJ ;
ROSENBERG, SA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1991, 173 (03) :647-658
[5]   PROLIFERATION OF HUMAN-MALIGNANT MELANOMAS IS INHIBITED BY ANTISENSE OLIGODEOXYNUCLEOTIDES TARGETED AGAINST BASIC FIBROBLAST GROWTH-FACTOR [J].
BECKER, D ;
MEIER, CB ;
HERLYN, M .
EMBO JOURNAL, 1989, 8 (12) :3685-3691
[6]   DIRECT INTRODUCTION OF GENES INTO RATS AND EXPRESSION OF THE GENES [J].
BENVENISTY, N ;
RESHEF, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (24) :9551-9555
[7]  
BERGMANN L, 1991, P ANN M AM ASS CANCE, V32, P1457
[8]   INHIBITION OF RABBIT GLOBIN MESSENGER-RNA TRANSLATION BY SEQUENCE-SPECIFIC OLIGODEOXYRIBONUCLEOTIDES [J].
BLAKE, KR ;
MURAKAMI, A ;
MILLER, PS .
BIOCHEMISTRY, 1985, 24 (22) :6132-6138
[9]   THE GTPASE SUPERFAMILY - A CONSERVED SWITCH FOR DIVERSE CELL FUNCTIONS [J].
BOURNE, HR ;
SANDERS, DA ;
MCCORMICK, F .
NATURE, 1990, 348 (6297) :125-132
[10]   A PHASE-II TRIAL OF RECOMBINANT TUMOR-NECROSIS-FACTOR IN PATIENTS WITH ADENOCARCINOMA OF THE PANCREAS - A SOUTHWEST ONCOLOGY GROUP-STUDY [J].
BROWN, TD ;
GOODMAN, P ;
FLEMING, T ;
MACDONALD, JS ;
HERSH, EM ;
BRAUN, TJ .
JOURNAL OF IMMUNOTHERAPY, 1991, 10 (05) :376-378