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通过整合多个数据集预测特定阶段的癌症相关基因及其动态模块。

Predicting stage-specific cancer related genes and their dynamic modules by integrating multiple datasets.

机构信息

School of Computer Science, Northwestern Polytechnical University, Xi'an, 710072, China.

Key Laboratory of Big Data Storage and Management, Northwestern Polytechnical University Ministry of Industry and Information Technology, Xi'an, China.

出版信息

BMC Bioinformatics. 2019 May 1;20(Suppl 7):194. doi: 10.1186/s12859-019-2740-6.

DOI:10.1186/s12859-019-2740-6
PMID:31074385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6509867/
Abstract

BACKGROUND

The mechanism of many complex diseases has not been detected accurately in terms of their stage evolution. Previous studies mainly focus on the identification of associations between genes and individual diseases, but less is known about their associations with specific disease stages. Exploring biological modules through different disease stages could provide valuable knowledge to genomic and clinical research.

RESULTS

In this study, we proposed a powerful and versatile framework to identify stage-specific cancer related genes and their dynamic modules by integrating multiple datasets. The discovered modules and their specific-signature genes were significantly enriched in many relevant known pathways. To further illustrate the dynamic evolution of these clinical-stages, a pathway network was built by taking individual pathways as vertices and the overlapping relationship between their annotated genes as edges.

CONCLUSIONS

The identified pathway network not only help us to understand the functional evolution of complex diseases, but also useful for clinical management to select the optimum treatment regimens and the appropriate drugs for patients.

摘要

背景

许多复杂疾病的机制在其阶段演变方面尚未得到准确检测。以前的研究主要集中在鉴定基因与个体疾病之间的关联,但对它们与特定疾病阶段的关联知之甚少。通过不同的疾病阶段探索生物模块可以为基因组学和临床研究提供有价值的知识。

结果

在这项研究中,我们提出了一个强大而通用的框架,通过整合多个数据集来识别特定阶段的癌症相关基因及其动态模块。发现的模块及其特定特征基因在许多相关的已知途径中显著富集。为了进一步说明这些临床阶段的动态演变,通过将单个途径作为顶点,将注释基因之间的重叠关系作为边,构建了一个途径网络。

结论

所鉴定的途径网络不仅有助于我们理解复杂疾病的功能演变,而且对于临床管理也很有用,可以为患者选择最佳治疗方案和合适的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/82062177dcce/12859_2019_2740_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/3999bf567113/12859_2019_2740_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/df5536e40a23/12859_2019_2740_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/2a1af9f4e8bc/12859_2019_2740_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/314122c794fc/12859_2019_2740_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/bff1639cea62/12859_2019_2740_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/f3d52bf92682/12859_2019_2740_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/54c599c3a341/12859_2019_2740_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/82062177dcce/12859_2019_2740_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/3999bf567113/12859_2019_2740_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/df5536e40a23/12859_2019_2740_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/2a1af9f4e8bc/12859_2019_2740_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/314122c794fc/12859_2019_2740_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/bff1639cea62/12859_2019_2740_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/f3d52bf92682/12859_2019_2740_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/54c599c3a341/12859_2019_2740_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d68d/6509867/82062177dcce/12859_2019_2740_Fig8_HTML.jpg

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本文引用的文献

1
CSTEA: a webserver for the Cell State Transition Expression Atlas.CSTEA:细胞状态转换表达图谱的网络服务器。
Nucleic Acids Res. 2017 Jul 3;45(W1):W103-W108. doi: 10.1093/nar/gkx402.
2
A scored human protein-protein interaction network to catalyze genomic interpretation.一个用于催化基因组解读的评分人类蛋白质-蛋白质相互作用网络。
Nat Methods. 2017 Jan;14(1):61-64. doi: 10.1038/nmeth.4083. Epub 2016 Nov 28.
3
Integrative analysis of mutational and transcriptional profiles reveals driver mutations of metastatic breast cancers.整合突变和转录谱分析揭示转移性乳腺癌的驱动突变。
双向整流法通过最大化共功能关系来识别差异表达基因。
BMC Genomics. 2021 Jun 25;22(Suppl 1):471. doi: 10.1186/s12864-021-07772-2.
Cell Discov. 2016 Aug 30;2:16025. doi: 10.1038/celldisc.2016.25. eCollection 2016.
4
The Cancer Genome Atlas Clinical Explorer: a web and mobile interface for identifying clinical-genomic driver associations.癌症基因组图谱临床浏览器:用于识别临床基因组驱动因素关联的网络和移动界面。
Genome Med. 2015 Oct 27;7:112. doi: 10.1186/s13073-015-0226-3.
5
Prediction of early breast cancer metastasis from DNA microarray data using high-dimensional cox regression models.使用高维Cox回归模型从DNA微阵列数据预测早期乳腺癌转移
Cancer Inform. 2015 May 5;14(Suppl 2):129-38. doi: 10.4137/CIN.S17284. eCollection 2015.
6
Multiplatform analysis of 12 cancer types reveals molecular classification within and across tissues of origin.对12种癌症类型的多平台分析揭示了原发组织内部和之间的分子分类。
Cell. 2014 Aug 14;158(4):929-944. doi: 10.1016/j.cell.2014.06.049. Epub 2014 Aug 7.
7
Neuropsychosocial profiles of current and future adolescent alcohol misusers.当前和未来青少年酒精滥用者的神经心理社会特征。
Nature. 2014 Aug 14;512(7513):185-9. doi: 10.1038/nature13402. Epub 2014 Jul 2.
8
Evolutionary mechanism unifies the hallmarks of cancer.进化机制统一了癌症的特征。
Int J Cancer. 2015 May 1;136(9):2012-21. doi: 10.1002/ijc.29031. Epub 2014 Jun 30.
9
Stress, genomic adaptation, and the evolutionary trade-off.压力、基因组适应和进化权衡。
Front Genet. 2014 Apr 23;5:92. doi: 10.3389/fgene.2014.00092. eCollection 2014.
10
The transcriptional regulatory network of proneural glioma determines the genetic alterations selected during tumor progression.神经前体细胞胶质瘤的转录调控网络决定了肿瘤进展过程中选择的遗传改变。
Cancer Res. 2014 Mar 1;74(5):1440-1451. doi: 10.1158/0008-5472.CAN-13-2150. Epub 2014 Jan 3.