Improving enzymes for cancer gene therapy

被引:51
作者
Encell, LP
Landis, DM
Loeb, LA
机构
[1] Univ Washington, Sch Med, Dept Pathol, Joseph Gottstein Mem Canc Res Lab, Seattle, WA 98195 USA
[2] Univ Washington, Sch Med, Dept Biochem, Seattle, WA 98195 USA
关键词
directed evolution; gene therapy; myelosuppression; protein engineering; tumor ablation;
D O I
10.1038/6142
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
New techniques now make it feasible to tailor enzymes for cancer gene therapy. Novel enzymes with desired properties can be created and selected from vast libraries of mutants containing random substitutions within catalytic domains. In this review, we first consider genes for the ablation of tumors, namely, genes that have been mutated (or potentially can be mutated) to afford enhanced activation of prodrugs and increased sensitization of tumors to specific chemotherapeutic agents. We then consider genes that have been mutated to provide better protection of normal host tissues, such as bone marrow, against the toxicity of specific chemotherapeutic agents. Expression of the mutant enzyme could render sensitive tissues, such as bone marrow, more resistant to specific cytotoxic agents.
引用
收藏
页码:143 / 147
页数:5
相关论文
共 56 条
  • [1] GENE-THERAPY UTILIZING DRUG-RESISTANCE GENES - A REVIEW
    BANERJEE, D
    ZHAO, SC
    LI, MX
    SCHWEITZER, BI
    MINEISHI, S
    BERTINO, JR
    [J]. STEM CELLS, 1994, 12 (04) : 378 - 385
  • [2] BARBOUR KW, 1990, MOL PHARMACOL, V37, P515
  • [3] IN-VITRO EVIDENCE THAT METABOLIC COOPERATION IS RESPONSIBLE FOR THE BYSTANDER EFFECT OBSERVED WITH HSV TK RETROVIRAL GENE-THERAPY
    BI, WL
    PARYSEK, LM
    WARNICK, R
    STAMBROOK, PJ
    [J]. HUMAN GENE THERAPY, 1993, 4 (06) : 725 - 731
  • [4] Creation of drug-specific herpes simplex virus type 1 thymidine kinase mutants for gene therapy
    Black, ME
    Newcomb, TG
    Wilson, HMP
    Loeb, LA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (08) : 3525 - 3529
  • [5] IDENTIFICATION OF IMPORTANT RESIDUES WITHIN THE PUTATIVE NUCLEOSIDE BINDING-SITE OF HSV-1 THYMIDINE KINASE BY RANDOM SEQUENCE SELECTION - ANALYSIS OF SELECTED MUTANTS IN-VITRO
    BLACK, ME
    LOEB, LA
    [J]. BIOCHEMISTRY, 1993, 32 (43) : 11618 - 11626
  • [6] Gene transfer and the treatment of childhood cancer
    Brenner, MK
    [J]. CANCER INVESTIGATION, 1998, 16 (04) : 269 - 278
  • [7] CADWELL RC, 1994, PCR METH APPL, V3, pS136
  • [8] CHAKRAVARTI D, 1991, J BIOL CHEM, V266, P15710
  • [9] Chemoprotective gene transfer II:: Multilineage in vivo protection of haemopoiesis against the effects of an antitumour agent by expression of a mutant human O6-alkylguanine-DNA alkyltransferase
    Chinnasamy, N
    Rafferty, JA
    Hickson, I
    Lashford, LS
    Longhurst, SJ
    Thatcher, N
    Margison, GP
    Dexter, TM
    Fairbairn, LJ
    [J]. GENE THERAPY, 1998, 5 (06) : 842 - 847
  • [10] Christians FC, 1997, CANCER RES, V57, P2007