[1]毛玉杰,魏东,李玉双.采用偏最小二乘法的基因-药物共模块识别[J].华侨大学学报(自然科学版),2020,41(1):121-125.[doi:10.11830/ISSN.1000-5013.201903012]
 MAO Yujie,WEI Dong,LI Yushuang.Identify Gene-Drug Co-Modules by Partial Least Square Method[J].Journal of Huaqiao University(Natural Science),2020,41(1):121-125.[doi:10.11830/ISSN.1000-5013.201903012]
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采用偏最小二乘法的基因-药物共模块识别()
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《华侨大学学报(自然科学版)》[ISSN:1000-5013/CN:35-1079/N]

卷:
第41卷
期数:
2020年第1期
页码:
121-125
栏目:
出版日期:
2020-01-20

文章信息/Info

Title:
Identify Gene-Drug Co-Modules by Partial Least Square Method
文章编号:
1000-5013(2020)01-0121-05
作者:
毛玉杰1 魏东12 李玉双1
1. 燕山大学 理学院, 河北 秦皇岛 066004;2. 河北数港科技有限公司, 河北 秦皇岛 066004
Author(s):
MAO Yujie1 WEI Dong12 LI Yushuang1
1. School of Science, Yanshan University, Qinhuangdao 066004, China; 2. Hebei Dataport Technology Limited Company, Qinhuangdao 066004, China
关键词:
偏最小二乘算法 药物关联网络 基因模块 药物模块 基因-药物共模块
Keywords:
partial least square algorithm drug association network gene module drug module gene-drug co-module
分类号:
Q332
DOI:
10.11830/ISSN.1000-5013.201903012
文献标志码:
A
摘要:
首先,将药物二维化学结构转化为数值序列,计算药物之间的皮尔逊相关系数,进而构建药物关联网络;然后,在带有基因网络约束的稀疏偏最小二乘算法的基础上,加入药物关联网络信息,提出伴有基因和药物关联网络正则约束的稀疏偏最小二乘(SGDPLS)算法;最后,将SGDPLS算法应用于基因-药物共模块识别.结果表明:药物关联网络信息的加入能够有效提高所识别的共模块中基因模块与药物模块的相关性,增加共模块的生物可解释性.
Abstract:
First, we transform the two-dimensional chemical structures of drugs into digital sequences, calculate the Pearson correlation coefficients between drugs, and then construct a drug association network. Next, we incorporate the information from drug association network into sparse partial least square algorithm with gene network, and presente the sparse partial least square algorithm with gene and drug association networks(SGDPLS)algorithm. Finally, we apply SGDPLS algorithm to identify gene-drug co-modules. The result shows that, the addition of drug association network can improve the correlations between the gene modules and drug modules identified from the common module, and enhance the interpretability of the modules.

参考文献/References:

[1] BARRETINA J,CAPONIGRO G,STRANSKY N,et al.The cancer cell line encyclopedia enables predictive modelling of anticancer drug sensitivity[J].Nature,2012,483(7391):603-607.DOI:10.1038/nature11003.
[2] GARNETT M J,EDELMAN E J,HEIDORN S J,et al.Systematic identification of genomic markers of drug sensitivity in cancer cells[J].Nature,2012,483(7391):570-575.DOI:10.1038/nature11005.
[3] BOKHARI S U,GOPAL U M,DUCKWORTH W C.Beneficial effects of a glyburide/metformin combination preparation in type 2 diabetes mellitus[J].American Journal of the Medical Sciences,2003,325(2):66-69.DOI:DOI:10.1097/00000441-200302000-00003.
[4] 胡尊胜,林锦贤,吕暾.蛋白质界面网络中模体和模块的探测[J].华侨大学学报(自然科学版),2014,35(1):61-66.DOI:10.11830/issn.1000-5013.2014.01.0061.
[5] ZHANG Shihua,LI Qingjiao,LIU Juan,et al.A novel computational framework for simultaneous integration of multiple types of genomic data to identify microRNA-gene regulatory modules[J].Bioinformatics,2011,27(13):i401-i409.DOI:10.1093/bioinformatics/btr206.
[6] CHEN Jinyu,ZHANG Shihua.Integrative analysis for identifying joint modular patterns of gene-expression and drug-response data[J].Bioinformatics,2016,32(11):1724-1732.DOI:10.1093/bioinformatics/btw059.
[7] WANG Lin,LI Xiaozhong,ZHANG Louxin,et al.Improved anticancer drug response prediction in cell lines using matrix factorization with similarity regularization[J].BMC Cancer,2017,17(1):513.DOI:10.1186/s12885-017-3500-5.
[8] LUXDURG U V.A tutorial on spectral clustering[J].Statistics and Computing,2007,17(4):395-416.DOI:10.1007/s11222-007-9033-z.
[9] OLESZKO A,HARTWICH J,WÓJTOWICZ A,et al.Comparison of FTIR-ATR and Raman spectroscopy in determination of VLDL triglycerides in blood serum with PLS regression[J].Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy,2017,183:239-246.DOI:10.1016/j.saa.2017.04.020.
[10] WANG Bei,CHEN Jinyu,ZHANG Shihua.BMTK: A toolkit for determining modules in biological bipartite networks[J].Quantitative Biology,2018,6(2):186-192.DOI:10.1007/s40484-018-0132-y.
[11] JALLEPALLI P V,LENGAUER C.Chromosome segregation and cancer: Cutting through the mystery[J].Nature Reviews Cancer,2001,1(2):109.DOI:10.1038/35101065.
[12] RIICHIROH M,YUTAKA N,TOMOHIDE T,et al.Phase Ⅲ study, V-15-32, of gefitinib versus docetaxel in previously treated Japanese patients with non-small-cell lung cancer[J].Journal of Clinical Oncology,2008,26(26):4244-4252.DOI:10.1200/JCO.2007.15.0185.
[13] DILLY A K,SONG X,ZEH H J,et al.Mitogen-activated protein kinase inhibition reduces mucin 2 production and mucinous tumor growth[J].Translational Research,2015,166(4):344-354.DOI:10.1016/j.trsl.2015.03.004.
[14] IVERSON C,LARSON G,LAI C,et al.RDEA119/BAY 869766: A potent, selective, allosteric inhibitor of MEK1/2 for the treatment of cancer[J].Cancer Research,2009,69(17):6839-6847.DOI:10.1158/0008-5472.can-09-0679.
[15] 华正宇.基于SLT的偏最小二乘分类算法及其优化方法研究[D].沈阳:东北大学,2013.

备注/Memo

备注/Memo:
收稿日期: 2019-03-06
通信作者: 李玉双(1980-),女,教授,博士,主要从事生物数学的研究.E-mail:yushuangli@ysu.edu.cn.
基金项目: 国家自然科学基金资助项目(61807029)
更新日期/Last Update: 2020-01-20