The effects of three bioreductive drugs (mitomycin C, RSU-1069 and SR4233) on cell lines selected for their sensitivity to mitomycin C or ionising radiation.
The effects of three bioreductive drugs (mitomycin C, RSU-1069 and SR4233) on cell lines selected for their sensitivity to mitomycin C or ionising radiation.
复制标题
三种生物还原药物(丝裂霉素 C、RSU-1069 和 SR4233)对因对丝裂霉素 C 或电离辐射敏感而选择的细胞系的影响。
DOI:
10.1038/bjc.1990.162
复制
发表时间:
1990
影响因子:
8.8
通讯作者:
Adams,GE
中科院分区:
文献类型:
--
作者:
Keohane,A;Godden,J;Stratford,IJ;Adams,GE
We have investigated the cross-sensitivity of a number of cell lines to three different classes of bioreductive drugs under both aerobic and hypoxic conditions. The cell lines used were selected for their sensitivity to DNA-damaging agents and fall into two groups. One group, MMC cells derived from CHO-K1 cells (Robson et al., 1985), show a range of sensitivities to mitomycin C in air. The second group, irs cells were cloned from V79 Chinese hamster fibroblasts (Jones et al., 1987) and exhibit sensitivity to ionising radiation. The sensitivity of both groups of cells to mitomycin C (MMC), RSU-1069 and SR4233 was assessed under aerobic and hypoxic conditions. No difference in aerobic or hypoxic toxicity of MMC was observed for CHO-K1 or MMC sensitive cell lines (MMC-2 and MMC-3). However, the MMC-resistant cell line (MMCr) was 10 times more sensitive under hypoxic than aerobic conditions. This suggests that MMCr cells lack or are deficient in the enzymes responsible for activating MMC under aerobic conditions compared to other MMC cells. In contrast, differential toxicities of between 3 and 30 have been observed for all CHO cells treated with RSU-1069 and SR4233. Treatment of V79 and irs cells with RSU-1069 and SR4233 also resulted in selective toxicity towards hypoxic cells. Differential toxicities between 50 and 100 were observed for V79 cells. For both RSU-1069 and SR4233, the hypoxic toxicities were similar in V79 and irs cells but in air, the radiation sensitive cells were up to 10 times more sensitive than wild type cells.
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DOI:
10.1016/0006-291x(75)90163-1
发表时间:
1975-01-01
影响因子:
3.1
作者:
MASON, RP;HOLTZMAN, JL
通讯作者:
HOLTZMAN, JL
影响因子:
11.2
作者:
Keyes,SR;Fracasso,PM;Heimbrook,DC;Rockwell,S;Sligar,SG;Sartorelli,AC
通讯作者:
Sartorelli,AC
DOI:
10.1016/0360-3016(89)90900-0
发表时间:
1989-04-01
影响因子:
7
作者:
WALTON, MI;WOLF, CR;WORKMAN, P
通讯作者:
WORKMAN, P
影响因子:
5.8
作者:
I. Stratford;P. O'Neill;P. Sheldon;A. Silver;J. Walling;G. Adams
通讯作者:
G. Adams
DOI:
10.1016/0921-8777(90)90057-c
发表时间:
1990
期刊:
Mutation research
影响因子:
--
作者:
J. Thacker;A. Ganesh
通讯作者:
A. Ganesh