首页> 外文期刊>The lancet oncology >Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study.
【24h】

Arg462Gln sequence variation in the prostate-cancer-susceptibility gene RNASEL and age of onset of hereditary non-polyposis colorectal cancer: a case-control study.

机译:前列腺癌敏感性基因RNASEL中的Arg462Gln序列变异和遗传性非息肉性结直肠癌的发病年龄:病例对照研究。

获取原文
获取原文并翻译 | 示例
           

摘要

BACKGROUND: RNASEL is thought to be a susceptibility gene for hereditary prostate cancer and encodes the endoribonuclease RNase L, which has a role in apoptosis and is a candidate tumour-suppressor protein. A common sequence variation in RNASEL, Arg462Gln, has been associated with hereditary and sporadic prostate cancer, and the Gln variant has about three-fold reduced RNase activity in vitro. In view of the association between the age of onset of hereditary non-polyposis colorectal cancer and functionally different variants of P53, which play a key part in the apoptotic pathway, we aimed to assess whether the Arg462Gln variation of RNASEL affects the age of onset of hereditary non-polyposis colorectal cancer. METHODS: We screened 251 patients with hereditary non-polyposis colorectal cancer who were unrelated, had pathogenic germline mutations in MSH2 (n=141) or MLH1 (n=110), and had colorectal carcinoma as the first tumour, for variation at codon 462 of RNASEL and compared them with 439 healthy controls. FINDINGS: The median age of onset was 40 years (range 17-75) for patients with an Arg/Arg genotype at codon 462, 37 years (13-69) for patients with an Arg/Gln genotype, and 34 years (20-49) for those with a Gln/Gln genotype (p=0.0198). Only the RNASEL genotype had a significant effect on age of onset (p=0.0062) in an additive mode of inheritance. Pair-wise comparisons between genotype groups showed that the two homozygous groups (ie, Arg/Arg vs Gln/Gln) differed significantly in age of disease onset (mean age difference 4.8 years [SD 1.7], p=0.0044). INTERPRETATION: A sequence variation in the prostate-cancer-susceptibility gene RNASEL has a role in a different, unassociated malignant disease. Genotypes at RNASEL codon 462 are associated with age of onset of hereditary non-polyposis colorectal cancer in a dose-dependent way, and might have a role in preventive strategies for this disease.
机译:背景:RNASEL被认为是遗传性前列腺癌的易感基因,编码内切核糖核酸酶RNase L,后者在细胞凋亡中起着重要作用,是一种候选的肿瘤抑制蛋白。 RNASEL的常见序列变异Arg462Gln与遗传性和散发性前列腺癌有关,Gln变异体在体外的RNase活性降低了约三倍。鉴于遗传性非息肉病性结直肠癌的发病年龄与P53的功能不同变异(在凋亡途径中起关键作用)之间的关联,我们旨在评估RNA SEL的Arg462Gln变异是否会影响P53的发病年龄。遗传性非息肉性大肠癌。方法:我们筛选了不相关的遗传性非息肉性大肠直肠癌患者251位,其中MSH2(n = 141)或MLH1(n = 110)的致病性生殖系突变,并且以大肠癌为首发肿瘤,其密码子为462 RNASEL的检测,并将其与439位健康对照者进行比较。结果:Arg / Arg基因型在462位密码子的患者中位发病年龄为40岁(17-75岁),Arg / Gln基因型患者的中位发病年龄为34岁(20-岁)。 49)对于具有Gln / Gln基因型的患者(p = 0.0198)。在加性遗传模式中,只有RNASEL基因型对发病年龄有显着影响(p = 0.0062)。基因型组之间的成对比较显示,两个纯合组(即Arg / Arg与Gln / Gln)在疾病发作年龄方面存在显着差异(平均年龄差异4.8岁[SD 1.7],p = 0.0044)。解释:前列腺癌易感基因RNASEL的序列变异在另一种不相关的恶性疾病中起作用。 RNASEL密码子462的基因型与遗传性非息肉性结直肠癌的发病年龄呈剂量依赖性,并且可能在该疾病的预防策略中起作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号