Gene transfer to suppress bone marrow alkylation sensitivity

被引:13
作者
Roth, RB [1 ]
Samson, LD [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Canc Cell Biol, Boston, MA 02115 USA
关键词
O-6-methylguanine DNA methyltransferase; MGMT gene transfer; gene therapy; alkylating agent; DNA repair; bone marrow;
D O I
10.1016/S1383-5742(00)00021-1
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
Alkylating agents represent a highly cytotoxic class of chemotherapeutic compounds that are extremely effective anti-tumor agents. Unfortunately, alkylating agents damage both malignant and non-malignant tissues. Bone marrow is especially sensitive to damage by alkylating agent chemotherapy, and is a dose-limiting tissue when treating cancer patients. One strategy to overcome bone marrow sensitivity to alkylating agent exposure involves gene transfer of the DNA repair protein O-6-ethylguanine DNA methyltransferase (O(6)MeG DNA MTase) into bone marrow cells. O(6)MeG DNA MTase is of particular interest because it functions to protect against the mutagenic, clastogenic and cytotoxic effects of many chemotherapeutic alkylating agents. By increasing the O(6)MeG DNA MTase repair capacity of bone marrow cells, it is hoped that this tissue will become alkylation resistant, thereby increasing the therapeutic window for the selective destruction of malignant tissue. In this review, the field of O(6)MeG DNA MTase gene transfer into bone marrow cells will be summarized with an emphasis placed on strategies used for suppressing the deleterious side effects of chemotherapeutic alkylating agent treatment. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:107 / 120
页数:14
相关论文
共 107 条
[1]   CYCLOPHOSPHAMIDE (CYTOXAN) - A REVIEW ON RELEVANT PHARMACOLOGY AND CLINICAL USES [J].
AHMED, AR ;
HOMBAL, SM .
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY, 1984, 11 (06) :1115-1126
[2]  
Allay JA, 1996, CLIN CANCER RES, V2, P1353
[3]  
Allay JA, 1997, EXP HEMATOL, V25, P1069
[4]   RETROVIRAL TRANSDUCTION AND EXPRESSION OF THE HUMAN ALKYLTRANSFERASE CDNA PROVIDES NITROSOUREA RESISTANCE TO HEMATOPOIETIC-CELLS [J].
ALLAY, JA ;
DUMENCO, LL ;
KOC, ON ;
LIU, L ;
GERSON, SL .
BLOOD, 1995, 85 (11) :3342-3351
[5]   Biomedicine - Lentiviral vectors - the promise of gene therapy within reach? [J].
Amado, RG ;
Chen, ISY .
SCIENCE, 1999, 285 (5428) :674-676
[6]  
BALTZER L, 1994, ONCOLOGY POCKET GUID
[7]   THE LEVEL OF DNA INTERSTRAND CROSSLINKING IN BONE-MARROW PARALLELS THE EXTENT OF MYELOSUPPRESSION IN MICE TREATED WITH 4 CHLOROETHYLNITROSOUREAS [J].
BEDFORD, P ;
BERGER, MR ;
EISENBRAND, G ;
SCHMAHL, D .
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 1984, 108 (01) :141-147
[8]   CHEMOTHERAPY OF PLASMA-CELL MYELOMA AND THE INCIDENCE OF ACUTE-LEUKEMIA [J].
BERGSAGEL, DE ;
BAILEY, AJ ;
LANGLEY, GR ;
MACDONALD, RN ;
WHITE, DF ;
MILLER, AB .
NEW ENGLAND JOURNAL OF MEDICINE, 1979, 301 (14) :743-748
[9]   LEUKEMIA AND PRELEUKEMIA AFTER ADJUVANT TREATMENT OF GASTROINTESTINAL CANCER WITH SEMUSTINE (METHYL-CCNU) [J].
BOICE, JD ;
GREENE, MH ;
KILLEN, JY ;
ELLENBERG, SS ;
KEEHN, RJ ;
MCFADDEN, E ;
CHEN, TT ;
FRAUMENI, JF .
NEW ENGLAND JOURNAL OF MEDICINE, 1983, 309 (18) :1079-1084
[10]   DEFECTIVE MISMATCH BINDING AND A MUTATOR PHENOTYPE IN CELLS TOLERANT TO DNA DAMAGE [J].
BRANCH, P ;
AQUILINA, G ;
BIGNAMI, M ;
KARRAN, P .
NATURE, 1993, 362 (6421) :652-654