SENSITIZATION OF X-IRRADIATED CHINESE-HAMSTER V79-CELLS BY DERIVATIVES OF PYRIMIDINE NUCLEOSIDES

被引:7
作者
HIRAOKA, W [1 ]
TANABE, K [1 ]
KUWABARA, M [1 ]
SATO, F [1 ]
MATSUDA, A [1 ]
UEDA, T [1 ]
机构
[1] HOKKAIDO UNIV,FAC PHARMACEUT SCI,SAPPORO,HOKKAIDO 060,JAPAN
关键词
Aromatic compounds - Biomolecules - Cytology - Ionizing radiation - Irradiation - Mammals - Radiation effects - Viruses;
D O I
10.1269/jrr.29.246
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The modification of the lethal effects of ionizing radiation on cultured mammalian cells by the pyrimidine nucleoside analogues, 3'-azido-2',3'-dideoxythymidine, 3'-amino-2',3'-dideoxythymidine, 2',3'-didehydro-2',3'- dideoxythymidine and 2',3'-didehydro-2',3'-dideoxycytidine, was investigated using X-irradiated log-phase Chinese hamster V79 cells. The exposure of the cells to these drugs (1-7.5 mM) for 3h after X irradiation reduced the cell survival. The killing efficiency was further enhanced by treating the cells with the drugs for 3h before X irradiation and continuing the treatment for 3h after X irradiation. These observations reveal that the nucleoside analogues, which are known as inhibitors of human immunodeficiency virus replication, have the ability to suppress cellular recovery from the radiation-induced potentially lethal state of X-irradiated cells. © 1988 Oxford University Press. All rights reserved.
引用
收藏
页码:246 / 254
页数:9
相关论文
共 16 条
[1]   BOTH 2',3'-DIDEOXYTHYMIDINE AND ITS 2',3'-UNSATURATED DERIVATIVE (2',3'-DI-DEOXYTHYMIDINENE) ARE POTENT AND SELECTIVE INHIBITORS OF HUMAN IMMUNODEFICIENCY VIRUS-REPLICATION INVITRO [J].
BABA, M ;
PAUWELS, R ;
HERDEWIJN, P ;
DECLERCQ, E ;
DESMYTER, J ;
VANDEPUTTE, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1987, 142 (01) :128-134
[2]   POTENT AND SELECTIVE ANTI-HTLV-III/LAV ACTIVITY OF 2',3'-DIDEOXYCYTIDINENE, THE 2',3'-UNSATURATED DERIVATIVE OF 2',3'-DIDEOXYCYTIDINE [J].
BALZARINI, J ;
PAUWELS, R ;
HERDEWIJN, P ;
DECLERCQ, E ;
COONEY, DA ;
KANG, GJ ;
DALAL, M ;
JOHNS, DG ;
BRODER, S .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 140 (02) :735-742
[3]  
Fricke H., 1966, RAD DOSIMETRY INSTRU, P167
[4]   PHOSPHORYLATION OF 3'-AZIDO-3'-DEOXYTHYMIDINE AND SELECTIVE INTERACTION OF THE 5'-TRIPHOSPHATE WITH HUMAN-IMMUNODEFICIENCY-VIRUS REVERSE-TRANSCRIPTASE [J].
FURMAN, PA ;
FYFE, JA ;
STCLAIR, MH ;
WEINHOLD, K ;
RIDEOUT, JL ;
FREEMAN, GA ;
LEHRMAN, SN ;
BOLOGNESI, DP ;
BRODER, S ;
MITSUYA, H ;
BARRY, DW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (21) :8333-8337
[5]   INHIBITORY EFFECT OF 2',3'-DIDEHYDRO-2',3'-DIDEOXYNUCLEOSIDES ON INFECTIVITY, CYTOPATHIC EFFECTS, AND REPLICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS [J].
HAMAMOTO, Y ;
NAKASHIMA, H ;
MATSUI, T ;
MATSUDA, A ;
UEDA, T ;
YAMAMOTO, N .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1987, 31 (06) :907-910
[6]  
HORWITZ J. P., 1966, TETRAHEDRON LETT, V13, P1343
[7]   NUCLEOSIDES .5. MONOMESYLATES OF 1-(2]-DEOXY-BETA-D-LYXOFURANOSYL)THYMINE [J].
HORWITZ, JP ;
CHUA, J ;
NOEL, M .
JOURNAL OF ORGANIC CHEMISTRY, 1964, 29 (07) :2076-&
[8]   NUCLEOSIDES .11. 2',3'-DIDEOXYCYTIDIN [J].
HORWITZ, JP ;
CHUA, J ;
NOEL, M ;
DONATTI, JT .
JOURNAL OF ORGANIC CHEMISTRY, 1967, 32 (03) :817-&
[9]   QUANTITATIVE ASPECTS OF REPAIR OF POTENTIALLY LETHAL DAMAGE IN MAMMALIAN-CELLS [J].
ILIAKIS, G ;
POHLIT, W .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1979, 36 (06) :649-658
[10]   SYNTHESIS AND BIOLOGICAL-ACTIVITY OF SEVERAL AMINO ANALOGS OF THYMIDINE [J].
LIN, TS ;
PRUSOFF, WH .
JOURNAL OF MEDICINAL CHEMISTRY, 1978, 21 (01) :109-112