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同步化的HeLa S3细胞在细胞周期中对辐射和化学致癌物的差异敏感性分析。III. 4-硝基喹啉1-氧化物及其衍生物。

Analyses of differential sensitivities of synchronized HeLa S3 cells to radiations and chemical carcinogens during the cell cycle. III. 4-Nitroquinoline 1-oxide and its derivatives.

作者信息

Watanabe M, Horikawa M

出版信息

Mutat Res. 1975 May;28(2):295-304. doi: 10.1016/0027-5107(75)90107-4.

DOI:10.1016/0027-5107(75)90107-4
PMID:806013
Abstract

Sensitivity to the chemical carcinogens 4-nitroquinoline 1-oxide (4-NQO) and 4-hydroxyaminoquinoline I-oxide (4-HAQO), during the cell cycle of synchronized HeLa S3 cells, decreases from the late S to the early G2 phases. Cells in other phases are relatively sensitive to both carcinogens. [3-H]4-NQO and [ 3-H]4-HAQO seem to be bound preferably more with cellular DNA of the mitotic phase to the middle of the S phase than with that of the late S phase in which the cells are rather insensitive to these carcinogens. However, we found no significant difference in the excision rates of these carcinogens from the DNA of HeLa S3 cells through the cell cycle. These findings indicate that the cyclic variation of 4-NQO and 4-HAQO cell survivals during the cell cycle may be due to the differences in the amounts of 4-NQO and 4-HAQO bound with cellular DNA.

摘要

在同步化的HeLa S3细胞的细胞周期中,对化学致癌物4-硝基喹啉1-氧化物(4-NQO)和4-羟基氨基喹啉1-氧化物(4-HAQO)的敏感性从S期后期到G2期早期逐渐降低。处于其他阶段的细胞对这两种致癌物相对敏感。[3-H]4-NQO和[3-H]4-HAQO似乎与有丝分裂期到S期中期的细胞DNA结合得比与S期后期的细胞DNA结合得更紧密,而S期后期的细胞对这些致癌物相当不敏感。然而,我们发现这些致癌物从HeLa S3细胞DNA中在整个细胞周期的切除率没有显著差异。这些发现表明,细胞周期中4-NQO和4-HAQO细胞存活率的周期性变化可能是由于与细胞DNA结合的4-NQO和4-HAQO量的差异。

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