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在英国,接触黄曲霉毒素会构成癌症风险吗?

Does aflatoxin exposure in the United Kingdom constitute a cancer risk?

作者信息

Harrison J C, Carvajal M, Garner R C

机构信息

Jack Birch Unit for Environmental Carcinogenesis, Department of Biology, University of York, Heslington, North Yorkshire, UK.

出版信息

Environ Health Perspect. 1993 Mar;99:99-105. doi: 10.1289/ehp.939999.

Abstract

Although the aflatoxins were discovered more than 30 years ago, there is still considerable controversy surrounding their human health effects. Most countries have introduced legislation to control the level of aflatoxins in food, but it is not known if these permitted levels still pose a significant cancer risk. Furthermore, it is unlikely that all the sources of human aflatoxin exposure have been discovered, nor if the liver is the only, or indeed, major target organ for aflatoxin-induced cancer in man. In our laboratory we have used both immunological and HPLC methods to examine human DNA from a variety of tissues and organs to identify and quantify aflatoxin DNA-adducts. We have already detected aflatoxin B1 (AFB1)-DNA adducts in formalin-fixed tissue from an acute poisoning incident in Southeast Asia. Here we have examined human colon and rectum DNA from normal and tumorous tissue obtained from cancer patients and colon, liver, pancreas, breast, and cervix DNA from autopsy specimens. AFB1-DNA adducts were detected in all tissue types examined and ranged from 0-60 adducts/10(6) nucleotides. Where sample size allowed, the adduct levels were confirmed by HPLC analysis. Tumor tissues tended to have higher adduct levels than normal tissue from the same individual, and levels generally increased with patient age. In samples analyzed by HPLC, the adducts present had the chromatographic properties of [8,9-dihydro-8-(N5-formyl)-2',5',6'-triamino-4'-oxo-(N5-pyramidyl) -9- hydroxy-aflatoxin B1, the ring-opened form of the AFB1-guanine adduct.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尽管黄曲霉毒素在30多年前就已被发现,但围绕其对人类健康的影响仍存在相当大的争议。大多数国家已出台立法来控制食品中的黄曲霉毒素水平,但尚不清楚这些允许的水平是否仍会带来重大的癌症风险。此外,人类接触黄曲霉毒素的所有来源不太可能都已被发现,也不清楚肝脏是否是黄曲霉毒素诱发人类癌症的唯一或主要靶器官。在我们实验室,我们使用免疫和高效液相色谱法检测了来自各种组织和器官的人类DNA,以识别和定量黄曲霉毒素-DNA加合物。我们已经在东南亚一起急性中毒事件的福尔马林固定组织中检测到黄曲霉毒素B1(AFB1)-DNA加合物。在此,我们检测了从癌症患者获得的正常和肿瘤组织的人类结肠和直肠DNA,以及尸检标本中的结肠、肝脏、胰腺、乳腺和宫颈DNA。在所检测的所有组织类型中均检测到AFB1-DNA加合物,范围为0至60个加合物/10(6)个核苷酸。在样本量允许的情况下,加合物水平通过高效液相色谱分析得到证实。肿瘤组织的加合物水平往往高于同一个体的正常组织,且水平通常随患者年龄增加而升高。在通过高效液相色谱分析的样本中,所存在的加合物具有[8,9-二氢-8-(N5-甲酰基)-2',5',6'-三氨基-4'-氧代-(N5-嘧啶基)-9-羟基黄曲霉毒素B1的色谱特性,即AFB1-鸟嘌呤加合物的开环形式。(摘要截稿于250词)

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