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在一项针对丹麦人的前瞻性研究中,淋巴细胞中的ERCC1、XPD和RAI mRNA水平与肺癌风险无关。

ERCC1, XPD and RAI mRNA levels in lymphocytes are not associated with lung cancer risk in a prospective study of Danes.

作者信息

Vogel Ulla, Nexø Bjørn A, Tjønneland Anne, Wallin Håkan, Hertel Ole, Raaschou-Nielsen Ole

机构信息

National Institute of Occupational Health, Lersø Parkallé 105, DK-2100 Copenhagen, Denmark.

出版信息

Mutat Res. 2006 Jan 29;593(1-2):88-96. doi: 10.1016/j.mrfmmm.2005.06.021. Epub 2005 Jul 28.

Abstract

Low DNA-repair capacity has been associated with increased risk of several types of cancer. mRNA levels of the nucleotide excision repair genes ERCC1 and XPD have been shown to correlate with the DNA-repair capacity. Likewise, mRNA levels of several DNA-repair genes including ERCC1 have been shown to be lower in lymphocytes from patients with lung cancer and head and neck cancer compared with healthy persons. In these studies, the low DNA-repair gene expression levels could be either a risk factor for disease or a consequence of the same. In this nested case-cohort study, which to our knowledge, is the first prospective study of DNA-repair gene mRNA levels as predictors of lung cancer, we have investigated the occurrence of lung cancer in relation to the mRNA level of the two DNA-repair genes ERCC1 and XPD and the NF kappaB inhibitor RAI in blood samples prior to disease. Among 54,220 members of a Danish prospective cohort study, 265 lung cancer cases were identified and a sub-cohort comprising 272 individuals was used for comparison. The expression levels of the three adjacent genes were found to be highly inter-correlated, to be higher in women compared to men and to be lower in older individuals. The incidence rate ratios for lung cancer in association with one log-unit increase (natural logarithm) in mRNA levels were 1.12 (CI=0.89-1.41) for ERCC1, 1.00 (CI=0.83-1.21) for XPD and 1.25 (0.89-1.74) for RAI. In conclusion, this study indicated no association between mRNA expression of the DNA-repair genes ERCC1 and XPD and risk of subsequent development of lung cancer.

摘要

低DNA修复能力与多种癌症风险增加有关。核苷酸切除修复基因ERCC1和XPD的mRNA水平已被证明与DNA修复能力相关。同样,与健康人相比,肺癌和头颈癌患者淋巴细胞中包括ERCC1在内的几种DNA修复基因的mRNA水平较低。在这些研究中,低DNA修复基因表达水平可能是疾病的危险因素,也可能是疾病的结果。在这项巢式病例对照研究中,据我们所知,这是第一项将DNA修复基因mRNA水平作为肺癌预测指标的前瞻性研究,我们调查了在疾病发生前血液样本中,肺癌的发生与两种DNA修复基因ERCC1和XPD以及NF-κB抑制剂RAI的mRNA水平之间的关系。在一项丹麦前瞻性队列研究的54220名成员中,确定了265例肺癌病例,并使用一个由272名个体组成的亚队列进行比较。发现这三个相邻基因的表达水平高度相互关联,女性高于男性,老年人低于年轻人。ERCC1的mRNA水平每增加一个对数单位(自然对数),肺癌的发病率比为1.12(CI = 0.89 - 1.41),XPD为1.00(CI = 0.83 - 1.21),RAI为1.25(0.89 - 1.74)。总之,这项研究表明DNA修复基因ERCC1和XPD的mRNA表达与随后发生肺癌的风险之间没有关联。

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