• 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

可能的单核苷酸多态性与癌症关系的计算预测

Computational Prediction of Probable Single Nucleotide Polymorphism-Cancer Relationships.

作者信息

Bakhtiari Shahab, Sulaimany Sadegh, Talebi Mehrdad, Kalhor Kabmiz

机构信息

Department of Biological Sciences, University of Kurdistan, Sanandaj, Iran.

Department of Computer Engineering, University of Kurdistan, Sanandaj, Iran.

出版信息

Cancer Inform. 2020 Jul 15;19:1176935120942216. doi: 10.1177/1176935120942216. eCollection 2020.

DOI:10.1177/1176935120942216
PMID:32728337
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7364831/
Abstract

Genetic variations such as single nucleotide polymorphisms (SNPs) can cause susceptibility to cancer. Although thousands of genetic variants have been identified to be associated with different cancers, the molecular mechanisms of cancer remain unknown. There is not a particular dataset of relationships between cancer and SNPs, as a bipartite network, for computational analysis and prediction. Link prediction as a computational graph analysis method can help us to gain new insight into the network. In this article, after creating a network between cancer and SNPs using SNPedia and Cancer Research UK databases, we evaluated the computational link prediction methods to foresee new SNP-Cancer relationships. Results show that among the popular scoring methods based on network topology, for relation prediction, the preferential attachment (PA) algorithm is the most robust method according to computational and experimental evidence, and some of its computational predictions are corroborated in recent publications. According to the PA predictions, rs1801394-Non-small cell lung cancer, rs4880-Non-small cell lung cancer, and rs1805794-Colorectal cancer are some of the best probable SNP-Cancer associations that have not yet been mentioned in any published article, and they are the most probable candidates for additional laboratory and validation studies. Also, it is feasible to improve the predicting algorithms to produce new predictions in the future.

摘要

单核苷酸多态性(SNP)等基因变异可导致癌症易感性。尽管已鉴定出数千种与不同癌症相关的基因变异,但癌症的分子机制仍然未知。目前还没有一个作为二分网络的癌症与SNP之间关系的特定数据集用于计算分析和预测。链接预测作为一种计算图分析方法,可以帮助我们获得对该网络的新见解。在本文中,我们使用SNPedia和英国癌症研究数据库创建了癌症与SNP之间的网络后,评估了计算链接预测方法以预见新的SNP-癌症关系。结果表明,在基于网络拓扑的流行评分方法中,对于关系预测,根据计算和实验证据,优先连接(PA)算法是最稳健的方法,其一些计算预测在最近的出版物中得到了证实。根据PA预测,rs1801394-非小细胞肺癌、rs4880-非小细胞肺癌和rs1805794-结直肠癌是一些尚未在任何已发表文章中提及的最有可能的SNP-癌症关联,它们是进一步实验室和验证研究的最有可能的候选对象。此外,改进预测算法以在未来产生新的预测是可行的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/262f843b05f6/10.1177_1176935120942216-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/6fd5e2b7a0eb/10.1177_1176935120942216-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/68e48981a859/10.1177_1176935120942216-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/262f843b05f6/10.1177_1176935120942216-fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/6fd5e2b7a0eb/10.1177_1176935120942216-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/68e48981a859/10.1177_1176935120942216-fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d4e4/7364831/262f843b05f6/10.1177_1176935120942216-fig3.jpg

相似文献

1
Computational Prediction of Probable Single Nucleotide Polymorphism-Cancer Relationships.可能的单核苷酸多态性与癌症关系的计算预测
Cancer Inform. 2020 Jul 15;19:1176935120942216. doi: 10.1177/1176935120942216. eCollection 2020.
2
A computational approach to distinguish somatic vs. germline origin of genomic alterations from deep sequencing of cancer specimens without a matched normal.一种计算方法,用于从无匹配正常样本的癌症标本深度测序中区分基因组改变的体细胞起源与种系起源。
PLoS Comput Biol. 2018 Feb 7;14(2):e1005965. doi: 10.1371/journal.pcbi.1005965. eCollection 2018 Feb.
3
Tag SNP selection in genotype data for maximizing SNP prediction accuracy.在基因型数据中选择标签单核苷酸多态性以最大化单核苷酸多态性预测准确性。
Bioinformatics. 2005 Jun;21 Suppl 1:i195-203. doi: 10.1093/bioinformatics/bti1021.
4
The role of complementary bipartite visual analytical representations in the analysis of SNPs: a case study in ancestral informative markers.互补二分视觉分析表示在 SNPs 分析中的作用:以祖先信息标记为例的研究。
J Am Med Inform Assoc. 2012 Jun;19(e1):e5-e12. doi: 10.1136/amiajnl-2011-000745.
5
Application of neural networks with back-propagation to genome-enabled prediction of complex traits in Holstein-Friesian and German Fleckvieh cattle.基于神经网络的反向传播算法在荷斯坦-弗里森牛和德国弗莱维赫牛基因组特征预测复杂性状中的应用。
Genet Sel Evol. 2015 Mar 31;47(1):22. doi: 10.1186/s12711-015-0097-5.
6
Predicting Triple-Negative Breast Cancer Subtype Using Multiple Single Nucleotide Polymorphisms for Breast Cancer Risk and Several Variable Selection Methods.利用多个乳腺癌风险单核苷酸多态性及多种变量选择方法预测三阴性乳腺癌亚型
Geburtshilfe Frauenheilkd. 2017 Jun;77(6):667-678. doi: 10.1055/s-0043-111602. Epub 2017 Jun 28.
7
[Colorectal cancer susceptibility genetic variants in tumor free and colorectal carcinoma bearing Hungarian population. Individual predisposition to cancer].[匈牙利无肿瘤及患结直肠癌人群中的结直肠癌易感性基因变异。个体的癌症易感性]
Orv Hetil. 2018 Oct;159(40):1614-1623. doi: 10.1556/650.2018.31129.
8
Computational analysis of simulated SNP interactions between 26 growth factor-related genes in a breast cancer association study.在乳腺癌关联研究中对 26 个生长因子相关基因之间模拟 SNP 相互作用的计算分析。
OMICS. 2011 Jun;15(6):399-407. doi: 10.1089/omi.2010.0028. Epub 2011 May 20.
9
Accuracy of prediction of simulated polygenic phenotypes and their underlying quantitative trait loci genotypes using real or imputed whole-genome markers in cattle.利用真实或推算的全基因组标记预测牛模拟多基因表型及其潜在数量性状位点基因型的准确性。
Genet Sel Evol. 2015 Dec 23;47:99. doi: 10.1186/s12711-015-0179-4.
10

引用本文的文献

1
Predicting cancer risk using machine learning on lifestyle and genetic data.利用机器学习对生活方式和基因数据进行癌症风险预测。
Sci Rep. 2025 Aug 19;15(1):30458. doi: 10.1038/s41598-025-15656-8.
2
Computational prediction of new therapeutic effects of probiotics.计算预测益生菌的新治疗效果。
Sci Rep. 2024 May 24;14(1):11932. doi: 10.1038/s41598-024-62796-4.
3
Graphylo: A deep learning approach for predicting regulatory DNA and RNA sites from whole-genome multiple alignments.Graphylo:一种用于从全基因组多序列比对中预测调控DNA和RNA位点的深度学习方法。

本文引用的文献

1
Machine learning identifies interacting genetic variants contributing to breast cancer risk: A case study in Finnish cases and controls.机器学习鉴定出导致乳腺癌风险的相互作用遗传变异:芬兰病例对照研究。
Sci Rep. 2018 Sep 3;8(1):13149. doi: 10.1038/s41598-018-31573-5.
2
SNP rs10800708 within the KIF14 miRNA binding site is linked with breast cancer.位于KIF14微小RNA结合位点内的单核苷酸多态性(SNP)rs10800708与乳腺癌相关。
Br J Biomed Sci. 2019 Jan;76(1):46-48. doi: 10.1080/09674845.2018.1509551. Epub 2018 Oct 26.
3
Bladder Cancer Genetic Susceptibility. A Systematic Review.
iScience. 2024 Jan 26;27(2):109002. doi: 10.1016/j.isci.2024.109002. eCollection 2024 Feb 16.
膀胱癌的遗传易感性。一项系统综述。
Bladder Cancer. 2018 Apr 26;4(2):215-226. doi: 10.3233/BLC-170159.
4
"NQO1 Gene C609T Polymorphism (dbSNP: rs1800566) and Digestive Tract Cancer Risk: A Meta-Analysis.".NQO1基因C609T多态性(dbSNP:rs1800566)与消化道癌风险:一项荟萃分析。
Nutr Cancer. 2018 May-Jun;70(4):557-568. doi: 10.1080/01635581.2018.1460674. Epub 2018 Apr 13.
5
Interaction between alcohol consumption and methylenetetrahydrofolate reductase polymorphisms in thyroid cancer risk: National Cancer Center cohort in Korea.酒精摄入与亚甲基四氢叶酸还原酶多态性在甲状腺癌风险中的相互作用:韩国国家癌症中心队列研究。
Sci Rep. 2018 Mar 6;8(1):4077. doi: 10.1038/s41598-018-22189-w.
6
Genetic polymorphisms in human telomerase reverse transcriptase (hTERT) gene polymorphisms do not associated with breast cancer in patients in a turkish population: hospital-based case-control study.人端粒酶逆转录酶(hTERT)基因多态性与土耳其人群乳腺癌患者不相关:基于医院的病例对照研究
Cell Mol Biol (Noisy-le-grand). 2018 Feb 28;64(3):108-115. doi: 10.14715/cmb/2018.64.1.3.
7
Single nucleotide polymorphisms and cancer susceptibility.单核苷酸多态性与癌症易感性。
Oncotarget. 2017 Nov 7;8(66):110635-110649. doi: 10.18632/oncotarget.22372. eCollection 2017 Dec 15.
8
tagging polymorphisms are associated with risk of non-small cell lung cancer in eastern Chinese Han population.标签多态性与中国东部汉族人群非小细胞肺癌风险相关。
Oncotarget. 2017 Dec 4;8(66):110326-110336. doi: 10.18632/oncotarget.22887. eCollection 2017 Dec 15.
9
Association between NAT2, CYP1A1, and CYP1A2 genotypes, heterocyclic aromatic amines, and prostate cancer risk: a case control study in Japan.N-乙酰基转移酶2(NAT2)、细胞色素P450 1A1(CYP1A1)和细胞色素P450 1A2(CYP1A2)基因多态性、杂环胺与前列腺癌风险之间的关联:日本的一项病例对照研究
Environ Health Prev Med. 2017 Oct 24;22(1):72. doi: 10.1186/s12199-017-0681-0.
10
Genetic variants as ovarian cancer first-line treatment hallmarks: A systematic review and meta-analysis.遗传变异作为卵巢癌一线治疗标志物:系统评价和荟萃分析。
Cancer Treat Rev. 2017 Dec;61:35-52. doi: 10.1016/j.ctrv.2017.10.001. Epub 2017 Oct 20.