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本文引用的文献

1
Alkylation of nucleic acids and metabolism of small doses of dimethylnitrosamine in the rat.大鼠体内核酸的烷基化作用及小剂量二甲基亚硝胺的代谢
Cancer Res. 1981 Aug;41(8):3128-32.
2
O6-alkylguanine-DNA alkyltransferase activity in human brain and brain tumors.人脑中及脑肿瘤中的O6-烷基鸟嘌呤-DNA烷基转移酶活性
Carcinogenesis. 1984 Jan;5(1):121-4. doi: 10.1093/carcin/5.1.121.
3
Radioimmunoassay of O6-methyldeoxyguanosine in DNA of cells alkylated in vitro and in vivo.体外和体内烷基化细胞DNA中O6-甲基脱氧鸟苷的放射免疫测定
Carcinogenesis. 1983 Dec;4(12):1605-9. doi: 10.1093/carcin/4.12.1605.
4
O4-ethyldeoxythymidine, but not O6-ethyldeoxyguanosine, accumulates in hepatocyte DNA of rats exposed continuously to diethylnitrosamine.在持续接触二乙基亚硝胺的大鼠肝细胞DNA中,O4-乙基脱氧胸苷会累积,而O6-乙基脱氧鸟苷则不会。
Proc Natl Acad Sci U S A. 1984 Mar;81(6):1692-5. doi: 10.1073/pnas.81.6.1692.
5
O(6)-methyldeoxyguanosine in oesophageal DNA among individuals at high risk of oesophageal cancer.食管癌高危个体食管DNA中的O(6)-甲基脱氧鸟苷
Int J Cancer. 1985 Dec 15;36(6):661-5. doi: 10.1002/ijc.2910360607.
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Urinary excretion of N-nitrosamino acids and nitrate by inhabitants of high- and low-risk areas for esophageal cancer in Northern China: endogenous formation of nitrosoproline and its inhibition by vitamin C.中国北方食管癌高、低发区居民尿中N-亚硝基氨基酸和硝酸盐的排泄:亚硝基脯氨酸的内源性形成及其被维生素C的抑制作用
Cancer Res. 1986 Mar;46(3):1485-91.
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Mechanisms of carcinogenesis induced by alkylating agents.烷化剂诱导的致癌机制。
Biochim Biophys Acta. 1985 Dec 17;823(2):111-45. doi: 10.1016/0304-419x(85)90009-5.
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The role of O6-methylguanine-DNA methyltransferase in cell survival, mutagenesis and carcinogenesis.
Mutat Res. 1985 Jan-Mar;145(1-2):1-16. doi: 10.1016/0167-8817(85)90034-3.
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A comparison of cell survival, mutation and persistence of putative promutagenic lesions in Chinese hamster cells exposed to BNU or MNU.对暴露于BNU或MNU的中国仓鼠细胞中细胞存活、突变及潜在促诱变损伤的持续性进行比较。
Carcinogenesis. 1986 Dec;7(12):1981-5. doi: 10.1093/carcin/7.12.1981.
10
Comparison of O6-alkylguanine-DNA alkyltransferase activity based on cellular DNA content in human, rat and mouse tissues.基于人、大鼠和小鼠组织细胞DNA含量的O6-烷基鸟嘌呤-DNA烷基转移酶活性比较。
Carcinogenesis. 1986 May;7(5):745-9. doi: 10.1093/carcin/7.5.745.

人体胃肠道组织DNA中烷基化损伤的检测

The detection of alkylation damage in the DNA of human gastrointestinal tissues.

作者信息

Hall C N, Badawi A F, O'Connor P J, Saffhill R

机构信息

Department of Surgery, Wythenshawe Hospital, Manchester.

出版信息

Br J Cancer. 1991 Jul;64(1):59-63. doi: 10.1038/bjc.1991.239.

DOI:10.1038/bjc.1991.239
PMID:1854628
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1977320/
Abstract

Damage arising from putative environmental sources has been found in the DNA of the gastric and colorectal mucosae of patients presenting with gastrointestinal disorders from the South Manchester area. O6-Methylguanine (O6-MeG) in the range 0.010- greater than 0.300 mu moles mole-1 adenine was heterogeneously distributed both between and within individuals. The pattern of alkylation of tissue DNA appears to differ when comparison is made between gastric and colorectal samples. Most of the gastric tumour DNA samples were alkylated (5/6; 0.087 +/- 0.097), whereas the DNA of the associated mucosa was alkylated less frequently (2/7) and to a lesser extent; (0.017 +/- 0.030; P = 0.07). Conversely, colorectal tumour DNA was alkylated infrequently (1/7) and to a lower extent (0.003 +/- 0.007) than the DNA of the adjacent mucosa (8/10 samples alkylated with a mean of 0.083 +/- 0.106; P = less than 0.01), or indeed of any other tissue. Although increased levels of DNA damage in tissue associated with malignant disease have been indicated by independent studies of DNA damage at other cancer sites, significant differences were not observed in the present report, neither was there any suggestion of a relationship with smoking or alcohol consumption. The data provided by this report indicate that exposure to putative environmental alkylating agents occurs in the UK at levels comparable to those previously detected in areas of higher cancer risk. Although we cannot determine the extent to which this DNA damage is attributable to normal background exposures, it is evident that the alkylation of tissue DNA occurs and is not uniform. In conjunction with other reports, therefore these differences may begin to provide indications of mechanisms that could be of relevance in the aetiology of gastrointestinal cancers.

摘要

在来自南曼彻斯特地区患有胃肠疾病的患者的胃和结肠直肠黏膜DNA中,已发现假定环境来源造成的损伤。0.010 - 大于0.300微摩尔每摩尔腺嘌呤范围内的O6-甲基鸟嘌呤(O6-MeG)在个体之间和个体内部均呈异质性分布。当比较胃和结肠直肠样本时,组织DNA的烷基化模式似乎有所不同。大多数胃肿瘤DNA样本发生了烷基化(5/6;0.087±0.097),而相关黏膜的DNA烷基化频率较低(2/7)且程度较轻(0.017±0.030;P = 0.07)。相反,结肠直肠肿瘤DNA烷基化频率较低(1/7)且程度低于相邻黏膜的DNA(8/10样本发生烷基化,平均值为0.083±0.106;P<0.01),实际上也低于任何其他组织。尽管在其他癌症部位对DNA损伤的独立研究表明,与恶性疾病相关的组织中DNA损伤水平有所增加,但在本报告中未观察到显著差异,也没有任何迹象表明与吸烟或饮酒有关。本报告提供的数据表明,在英国,接触假定的环境烷基化剂的水平与先前在癌症风险较高地区检测到的水平相当。尽管我们无法确定这种DNA损伤在多大程度上可归因于正常背景暴露,但很明显组织DNA的烷基化确实发生且并不均匀。因此,结合其他报告,这些差异可能开始为胃肠道癌症病因学中可能相关的机制提供线索。