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共济失调毛细血管扩张症细胞对博来霉素异常敏感。

Unusual sensitivity of ataxia telangiectasia cells to bleomycin.

作者信息

Taylor A M, Rosney C M, Campbell J B

出版信息

Cancer Res. 1979 Mar;39(3):1046-50.

PMID:85479
Abstract

Peripheral blood lymphocytes from four patients with ataxia telangiectasia (AT), an inherited disorder showing, among other features, radiosensitivity and a high frequency of cancers, were shown to be cytogenetically more sensitive to bleomycin than were lymphocytes from both normal individuals and a single patient with xeroderma pigmentosum. With cell survival techniques, a biphasic dose-response curve was seen for both normal and AT fibroblasts, although the AT cells showed a much lower survival. The increased sensitivity to bleomycin in AT cells might be expected since it is a radiomimetic drug, but more importantly the known action of bleomycin in producing DNA strand scission suggests that AT cells might be defective in rejoining a proportion of DNA strand breaks.

摘要

共济失调毛细血管扩张症(AT)是一种遗传性疾病,除其他特征外,还表现出放射敏感性和高癌症发生率。来自四名AT患者的外周血淋巴细胞在细胞遗传学上显示出比正常个体和一名着色性干皮病患者的淋巴细胞对博来霉素更敏感。使用细胞存活技术,正常和AT成纤维细胞均呈现双相剂量反应曲线,尽管AT细胞的存活率要低得多。鉴于博来霉素是一种拟辐射药物,AT细胞对其敏感性增加可能在意料之中,但更重要的是,博来霉素产生DNA链断裂的已知作用表明,AT细胞在修复一定比例的DNA链断裂方面可能存在缺陷。

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