• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Somatic mutations are frequent and increase with age in human kidney epithelial cells.

作者信息

Martin G M, Ogburn C E, Colgin L M, Gown A M, Edland S D, Monnat R J

机构信息

Department of Pathology, University of Washington, Seattle 98195, USA.

出版信息

Hum Mol Genet. 1996 Feb;5(2):215-21. doi: 10.1093/hmg/5.2.215.

DOI:10.1093/hmg/5.2.215
PMID:8824877
Abstract

We have used a primary cloning assay to determine the frequency of 6-thioguanine (TG)-resistant tubular epithelial cells in kidney tissue from 72 human donors ranging in age from 2 to 94 years. The frequency of TG-resistant mutants ranged from approximately 5 x 10(-5) for donors in the first decade of life to approximately 2.5 x 10(-4) for donors in the eighth and later decades of life. Two different statistical analyses indicated that this increase in mutant frequency is exponential with age. We also observed a 2-fold higher TG-resistant mutant frequency in nephrectomy kidneys containing a coincident renal carcinoma. DNA sequence analyses revealed HPRT gene mutations in each of 14 TG-resistant mutants from seven unrelated donors. Thirteen of these 14 mutants resulted from independent mutational events. These results suggest that somatic mutations are common in renal--and perhaps in other human--epithelia, and thus could play an important role in the genesis of age-associated disease.

摘要

相似文献

1
Somatic mutations are frequent and increase with age in human kidney epithelial cells.
Hum Mol Genet. 1996 Feb;5(2):215-21. doi: 10.1093/hmg/5.2.215.
2
The unexpected landscape of in vivo somatic mutation in a human epithelial cell lineage.人类上皮细胞谱系中体内体细胞突变的意外情况
Proc Natl Acad Sci U S A. 2002 Feb 5;99(3):1437-42. doi: 10.1073/pnas.032655699. Epub 2002 Jan 29.
3
Molecular analysis of spontaneous hypoxanthine phosphoribosyltransferase mutations in thioguanine-resistant HL-60 human leukemia cells.硫鸟嘌呤抗性HL-60人白血病细胞中次黄嘌呤磷酸核糖基转移酶自发突变的分子分析。
Cancer Res. 1989 Jan 1;49(1):81-7.
4
Spectrum of point mutations in the coding region of the hypoxanthine-guanine phosphoribosyltransferase (hprt) gene in human T-lymphocytes in vivo.体内人T淋巴细胞次黄嘌呤 - 鸟嘌呤磷酸核糖转移酶(hprt)基因编码区的点突变谱
Carcinogenesis. 1998 Apr;19(4):557-66. doi: 10.1093/carcin/19.4.557.
5
Molecular analysis of in vivo mutations induced by N-ethyl-N-nitrosourea in the autosomal Tk and the X-linked Hprt genes of mouse lymphocytes.N-乙基-N-亚硝基脲诱导的小鼠淋巴细胞常染色体Tk基因和X连锁Hprt基因体内突变的分子分析。
Environ Mol Mutagen. 1999;34(1):30-8.
6
Thioguanine-resistant mutant frequency in T-lymphocytes from a healthy human population.健康人群T淋巴细胞中硫鸟嘌呤抗性突变频率
Mutat Res. 1992 Feb;265(2):165-71. doi: 10.1016/0027-5107(92)90045-4.
7
Enhanced hprt mutant frequency but no significant difference in mutation spectrum between a smoking and a non-smoking human population.吸烟人群与非吸烟人群相比,hprt突变频率增加,但突变谱无显著差异。
Carcinogenesis. 1992 Sep;13(9):1625-31. doi: 10.1093/carcin/13.9.1625.
8
Molecular spectrum of background mutation at the hprt locus in human T-lymphocytes.人T淋巴细胞中次黄嘌呤磷酸核糖转移酶(hprt)基因座背景突变的分子谱。
Mutagenesis. 1993 Jan;8(1):43-9. doi: 10.1093/mutage/8.1.43.
9
Mutations induced by (-)-anti-11R,12S-dihydrodiol 13S,14R-epoxide of dibenzo[a,l]pyrene in the coding region of the hypoxanthine phosphoribosyltransferase (Hprt) gene in Chinese hamster V79 cells.二苯并[a,l]芘的(-)-反式-11R,12S-二氢二醇13S,14R-环氧化物在中国仓鼠V79细胞次黄嘌呤磷酸核糖基转移酶(Hprt)基因编码区诱导的突变。
Environ Mol Mutagen. 2003;41(2):131-9. doi: 10.1002/em.10136.
10
Quantification of thioguanine-resistant lymphocytes from mice irradiated in vivo.对体内受辐照小鼠的硫鸟嘌呤抗性淋巴细胞进行定量分析。
Environ Health Perspect. 1990 Aug;88:129-32. doi: 10.1289/ehp.9088129.

引用本文的文献

1
A Universal Duplex Sequencing Approach for Accurate Detection of Somatic Mutations.一种用于准确检测体细胞突变的通用双链测序方法。
bioRxiv. 2025 Sep 16:2025.09.14.676103. doi: 10.1101/2025.09.14.676103.
2
The Link between Autosomal Dominant Polycystic Kidney Disease and Chromosomal Instability: Exploring the Relationship.常染色体显性多囊肾病与染色体不稳定之间的联系:探索二者关系
Int J Mol Sci. 2024 Mar 2;25(5):2936. doi: 10.3390/ijms25052936.
3
From DNA damage to mutations: All roads lead to aging.从 DNA 损伤到突变:条条大路通向衰老。
Ageing Res Rev. 2021 Jul;68:101316. doi: 10.1016/j.arr.2021.101316. Epub 2021 Mar 9.
4
The oncogenic potential of a mutant TP53 gene explored in two spontaneous lung cancer mice models.两个自发性肺癌小鼠模型中探索突变 TP53 基因的致癌潜能。
BMC Cancer. 2020 Aug 8;20(1):738. doi: 10.1186/s12885-020-07212-6.
5
Germline mutation rates in young adults predict longevity and reproductive lifespan.年轻人的种系突变率可预测其寿命和生殖寿命。
Sci Rep. 2020 Jun 19;10(1):10001. doi: 10.1038/s41598-020-66867-0.
6
Systemic Metabolism, Its Regulators, and Cancer: Past Mistakes and Future Potential.全身代谢、其调节因子与癌症:过去的误区与未来的潜力
Front Endocrinol (Lausanne). 2019 Feb 12;10:65. doi: 10.3389/fendo.2019.00065. eCollection 2019.
7
Somatic Mutations in Renal Cyst Epithelium in Autosomal Dominant Polycystic Kidney Disease.常染色体显性多囊肾病中肾囊肿上皮的体细胞突变。
J Am Soc Nephrol. 2018 Aug;29(8):2139-2156. doi: 10.1681/ASN.2017080878. Epub 2018 Jul 24.
8
Cancer Immunotherapy: Whence and Whither.癌症免疫疗法:起源与发展方向
Mol Cancer Res. 2017 Jun;15(6):635-650. doi: 10.1158/1541-7786.MCR-16-0427. Epub 2017 Mar 29.
9
Mutation and catastrophe in the aging genome.衰老基因组中的突变与巨变
Exp Gerontol. 2017 Aug;94:34-40. doi: 10.1016/j.exger.2017.02.073. Epub 2017 Mar 2.
10
How "precise" is precision medicine in hematology?血液学中的精准医学有多“精准”?
Haematologica. 2017 Jan;102(1):4-6. doi: 10.3324/haematol.2016.155267.