The Prediction of Drug-Disease Correlation Based on Gene Expression Data

被引:9
作者
Cui, Hui [1 ,2 ,3 ]
Zhang, Menghuan [2 ,3 ]
Yang, Qingmin [3 ,4 ]
Li, Xiangyi [3 ]
Liebman, Michael [3 ,5 ]
Yu, Ying [6 ]
Xie, Lu [3 ]
机构
[1] ShanghaiTech Univ, Sch Life Sci & Technol, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Nutr Sci, Shanghai 200031, Peoples R China
[3] Shanghai Acad Sci & Technol, Shanghai Ctr Bioinformat Technol, Shanghai 201203, Peoples R China
[4] Shanghai Ocean Univ, Coll Food Sci & Technol, 999 Hu Cheng Huan Rd, Shanghai 201306, Peoples R China
[5] IPQ Analyt LLC, Strateg Med, Philadelphia, PA USA
[6] Tianjin Med Univ, Sch Basic Med Sci, Dept Pharmacol, Tianjin 30007, Peoples R China
基金
中国国家自然科学基金;
关键词
MELANOMA; COMBINATIONS; MODEL;
D O I
10.1155/2018/4028473
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The explosive growth of high-throughput experimental methods and resulting data yields both opportunity and challenge for selecting the correct drug to treat both a specific patient and their individual disease. Ideally, it would be useful and efficient if computational approaches could be applied to help achieve optimal drug-patient-disease matching but current efforts have met with limited success. Current approaches have primarily utilized the measureable effect of a specific drug on target tissue or cell lines to identify the potential biological effect of such treatment. While these efforts have met with some level of success, there exists much opportunity for improvement. This specifically follows the observation that, for many diseases in light of actual patient response, there is increasing need for treatment with combinations of drugs rather than single drug therapies. Only a few previous studies have yielded computational approaches for predicting the synergy of drug combinations by analyzing high-throughput molecular datasets. However, these computational approaches focused on the characteristics of the drug itself, without fully accounting for disease factors. Here, we propose an algorithm to specifically predict synergistic effects of drug combinations on various diseases, by integrating the data characteristics of disease-related gene expression profiles with drug-treated gene expression profiles. We have demonstrated utility through its application to transcriptome data, including microarray and RNASeq data, and the drug-disease prediction results were validated using existing publications and drug databases. It is also applicable to other quantitative profiling data such as proteomics data. We also provide an interactive web interface to allow our Prediction of Drug-Disease method to be readily applied to user data. While our studies represent a preliminary exploration of this critical problem, we believe that the algorithm can provide the basis for further refinement towards addressing a large clinical need.
引用
收藏
页数:6
相关论文
共 16 条
[1]  
Borisov N., 2017, CELL CYCLE, P1
[2]   Improved Survival with Vemurafenib in Melanoma with BRAF V600E Mutation [J].
Chapman, Paul B. ;
Hauschild, Axel ;
Robert, Caroline ;
Haanen, John B. ;
Ascierto, Paolo ;
Larkin, James ;
Dummer, Reinhard ;
Garbe, Claus ;
Testori, Alessandro ;
Maio, Michele ;
Hogg, David ;
Lorigan, Paul ;
Lebbe, Celeste ;
Jouary, Thomas ;
Schadendorf, Dirk ;
Ribas, Antoni ;
O'Day, Steven J. ;
Sosman, Jeffrey A. ;
Kirkwood, John M. ;
Eggermont, Alexander M. M. ;
Dreno, Brigitte ;
Nolop, Keith ;
Li, Jiang ;
Nelson, Betty ;
Hou, Jeannie ;
Lee, Richard J. ;
Flaherty, Keith T. ;
McArthur, Grant A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2011, 364 (26) :2507-2516
[3]   Distinct sets of genetic alterations in melanoma [J].
Curtin, JA ;
Fridlyand, J ;
Kageshita, T ;
Patel, HN ;
Busam, KJ ;
Kutzner, H ;
Cho, KH ;
Aiba, S ;
Bröcker, EB ;
LeBoit, PE ;
Pinkel, D ;
Bastian, BC .
NEW ENGLAND JOURNAL OF MEDICINE, 2005, 353 (20) :2135-2147
[4]   Genotype-Selective Combination Therapies for Melanoma Identified by High-Throughput Drug Screening [J].
Held, Matthew A. ;
Langdon, Casey G. ;
Platt, James T. ;
Graham-Steed, Tisheeka ;
Liu, Zongzhi ;
Chakraborty, Ashok ;
Bacchiocchi, Antonella ;
Koo, Andrew ;
Haskins, Jonathan W. ;
Bosenberg, Marcus W. ;
Stern, David F. .
CANCER DISCOVERY, 2013, 3 (01) :52-67
[5]  
Jia J., 2009, NAT REV DRUG DISCOV, V8, P516
[6]   An enhanced Petri-net model to predict synergistic effects of pairwise drug combinations from gene microarray data [J].
Jin, Guangxu ;
Zhao, Hong ;
Zhou, Xiaobo ;
Wong, Stephen T. C. .
BIOINFORMATICS, 2011, 27 (13) :I310-I316
[7]   DCDB 2.0: a major update of the drug combination database [J].
Liu, Yanbin ;
Wei, Qiang ;
Yu, Guisheng ;
Gai, Wanxia ;
Li, Yongquan ;
Chen, Xin .
DATABASE-THE JOURNAL OF BIOLOGICAL DATABASES AND CURATION, 2014,
[8]   Advair: Combination treatment with fluticasone propionate/salmeterol in the treatment of asthma [J].
Nelson, HS .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2001, 107 (02) :397-416
[9]   High-Throughput Sequencing Technologies [J].
Reuter, Jason A. ;
Spacek, Damek V. ;
Snyder, Michael P. .
MOLECULAR CELL, 2015, 58 (04) :586-597
[10]  
Sheng Z., 2017, BRIEFINGS BIOINFORMA