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人类外周血淋巴细胞诱变敏感性和DNA修复能力的快速筛选检测法。

Rapid screening assay for mutagen sensitivity and DNA repair capacity in human peripheral blood lymphocytes.

作者信息

Schmezer P, Rajaee-Behbahani N, Risch A, Thiel S, Rittgen W, Drings P, Dienemann H, Kayser K W, Schulz V, Bartsch H

机构信息

Division of Toxicology and Cancer Risk Factors, German Cancer Research Center, Heidelberg, Germany.

出版信息

Mutagenesis. 2001 Jan;16(1):25-30. doi: 10.1093/mutage/16.1.25.

Abstract

Individual susceptibility to carcinogens, an important determinant of disease risk, is influenced by host factors such as the ability to repair DNA lesions. In order to identify subjects who are at high risk, we have developed a microgel electrophoresis assay for use in molecular epidemiological studies. The assay was validated in a pilot case-control study: Peripheral blood lymphocytes were collected from 100 patients with lung cancer and 110 control patients without cancer and from the same hospital, and stored at -80 degrees C. After thawing, phytohaemagglutinin-stimulated cells were treated with bleomycin at 20 microg/ml for 30 min and the extent of DNA damage and DNA repair capacity were determined by microgel electrophoresis. Peripheral blood lymphocytes from patients with lung cancer were significantly more sensitive to mutagens than those from controls and showed reduced DNA repair capacity (both P < 0.001). Both endpoints were independent risk factors for smoking-related lung cancer. Repeated analysis of peripheral blood lymphocytes from the same individual demonstrated good reproducibility of the assay. Cryopreservation of the lymphocytes for less than or = 12 months did not significantly affect their sensitivity. Our standardized microgel electrophoresis assay is suitable for determining individual sensitivity to mutagens and DNA repair capacity: it is sensitive and faster than cytogenetic assays, and can be applied to native and cryopreserved peripheral blood lymphocytes.

摘要

个体对致癌物的易感性是疾病风险的一个重要决定因素,它受宿主因素如DNA损伤修复能力的影响。为了识别高危人群,我们开发了一种用于分子流行病学研究的微凝胶电泳检测方法。该检测方法在一项初步病例对照研究中得到验证:从同一家医院收集了100例肺癌患者和110例无癌症对照患者的外周血淋巴细胞,并储存在-80℃。解冻后,用20μg/ml博来霉素处理经植物血凝素刺激的细胞30分钟,通过微凝胶电泳测定DNA损伤程度和DNA修复能力。肺癌患者的外周血淋巴细胞对诱变剂的敏感性明显高于对照组,且DNA修复能力降低(P均<0.001)。这两个终点都是吸烟相关肺癌的独立危险因素。对同一个体的外周血淋巴细胞进行重复分析表明该检测方法具有良好的重复性。淋巴细胞冷冻保存时间小于或等于12个月对其敏感性无显著影响。我们标准化的微凝胶电泳检测方法适用于测定个体对诱变剂的敏感性和DNA修复能力:它比细胞遗传学检测方法更灵敏、更快,并且可应用于新鲜的和冷冻保存的外周血淋巴细胞。

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