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核苷酸切除修复基因 ERCC2/XPD 多态性与非霍奇金淋巴瘤风险。

Polymorphisms in the nucleotide excision repair gene ERCC2/XPD and risk of non-Hodgkin lymphoma.

机构信息

Department of Biology, University of York, York, YO10 5YW, United Kingdom.

出版信息

Cancer Epidemiol. 2009 Oct;33(3-4):257-60. doi: 10.1016/j.canep.2009.08.002. Epub 2009 Sep 6.

Abstract

Non-Hodgkin lymphoma (NHL) represents a complex group of B- and T-cell malignancies characterised by chromosomal translocations. Since defects in DNA repair result in an increased frequency of chromosomal aberrations it has been hypothesised that genetic variation in DNA repair may be associated with risk of NHL. To investigate the relationship between DNA repair and NHL we analysed polymorphisms in XPD (R156R, D312N, K751Q) using DNA collected in a UK population-based case-control study of lymphoma. We observed no association between genetic variation in XPD and risk of NHL. However, the XPD 751 Gln allele was associated with a two-fold decreased risk of diffuse large B-cell lymphoma (OR 0.56, 95% CI 0.34-0.92, p=0.02), the major subtype of NHL. Overall, our study identifies that XPD polymorphisms may be important in the aetiology of NHL although analysis of additional polymorphisms and extended haplotype studies are required to clarify their role.

摘要

非霍奇金淋巴瘤(NHL)是一组由染色体易位引起的 B 细胞和 T 细胞恶性肿瘤,其特征为染色体易位。由于 DNA 修复缺陷导致染色体畸变的频率增加,因此有人假设 DNA 修复的遗传变异可能与 NHL 的风险相关。为了研究 DNA 修复与 NHL 之间的关系,我们使用在英国淋巴瘤基于人群的病例对照研究中收集的 DNA 分析了 XPD(R156R、D312N、K751Q)的多态性。我们没有发现 XPD 基因多态性与 NHL 风险之间存在关联。然而,XPD 751 谷氨酰胺等位基因与弥漫性大 B 细胞淋巴瘤(OR 0.56,95%CI 0.34-0.92,p=0.02)的风险降低两倍相关,弥漫性大 B 细胞淋巴瘤是 NHL 的主要亚型。总的来说,我们的研究表明,XPD 多态性可能在 NHL 的发病机制中起重要作用,但需要进一步分析其他多态性和扩展单倍型研究以阐明其作用。

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