문헌 기반 중요 유전자와 PPI 네트워크를 이용한 약물 재창출의 새로운 방법
Identifying literature-based significant genes and discovering novel drug indications on PPI network
2
조회
0
다운로드
0
인용
0
참고문헌
키워드
초록
New drug development is time-consuming and costly. Hence, it is necessary to repurpose old drugs for finding new indication. We suggest the way that repurposing old drug using massive literature data and biological network. We supposed a disease-drug relationship can be available if signal pathways of the relationship include significant genes identified in literature data. This research is composed of three steps-identifying significant gene using co-occurrence in literature; analyzing the shortest path on biological network; and scoring a relationship with comparison between the significant genes and the shortest paths. Based on literatures, we identify significant genes based on the co-occurrence frequency between a gene and disease. With the network that include weight as possibility of interaction between genes, we use shortest paths on the network as signal pathways. We perform comparing genes that identified as significant gene and included on signal pathways, calculating the scores and then identifying the candidate drugs. With this processes, we show the drugs having new possibility of drug repurposing and the use of our method as the new method of drug repurposing.
Abstract
New drug development is time-consuming and costly. Hence, it is necessary to repurpose old drugs for finding new indication. We suggest the way that repurposing old drug using massive literature data and biological network. We supposed a disease-drug relationship can be available if signal pathways of the relationship include significant genes identified in literature data. This research is composed of three steps-identifying significant gene using co-occurrence in literature; analyzing the shortest path on biological network; and scoring a relationship with comparison between the significant genes and the shortest paths. Based on literatures, we identify significant genes based on the co-occurrence frequency between a gene and disease. With the network that include weight as possibility of interaction between genes, we use shortest paths on the network as signal pathways. We perform comparing genes that identified as significant gene and included on signal pathways, calculating the scores and then identifying the candidate drugs. With this processes, we show the drugs having new possibility of drug repurposing and the use of our method as the new method of drug repurposing.
참고문헌 (20)
- Oprea, T. I, "Drug repurposing: far beyond new targets for old drugs", The AAPPS journal, 14(4), pp.759~763 (2012)
- Liu, Zhichao, "In silico drug repositioning–what we need to know", Drug discovery today, 18(3), pp.110~115 (2013)
- Andronis, Christos, "Literature mining, ontologies and information visualization for drug repurposing", Briefings in bioinformatics, 12(4), pp.357~368 (2011)
- 장기업, "유사 약물 예측을 위한 텍스트 마이닝 기반의 새로운 약물 유사도 측정 방법", 한국정보기술학회논문지, 14(7), pp.127~137 (2016), 한국정보기술학회[DOI]
- Wu, Zikai, "Network-based drug repositioning", Molecular BioSystems, 9(6), pp.1268~1281 (2013)
- Cheng, Feixiong, "Prediction of drug-target interactions and drug repositioning via network-based inference", PLoS Comput Biol, 8(5), pp.ppe1002503~ (2012)
- Canese, Kathi, "The NCBI Handbook" (2013)
- Law, Vivian, "DrugBank 4.0: shedding new light on drug metabolism", Nucleic acids research, 42(D1), pp.D1091~D1097 (2014)
- Whirl-Carrillo, Michelle, "Pharmacogenomics Knowledge for Personalized Medicine", Clinical Pharmacology & Therapeutics, 92(4), pp.414~417 (2012)
- Maglott, Donna, "Entrez Gene: gene-centered information at NCBI", Nucleic acids Research, 39(suppl 1), pp.D52~D57 (2011)
- Kibbe, Warren A, "Disease Ontology 2015 update: an expanded and updated database of human diseases for linking biomedical knowledge through disease data", Nucleic acids research, 43(D1), pp.gku1011~ (2014)
- Davis, Allan Peter, "The Comparative Toxicogenomics Database's 10th year anniversary: update 2015", Nucleic acids research, 43(D1), pp.D914~D920 (2015)
- Lee, Insuk, "Prioritizing candidate disease genes by network-based boosting of genome-wide association data", Genome Research, 21(7), pp.1109~1121 (2011)
- Yang, Hong, "Therapeutic target database update 2016: enriched resource for bench to clinical drug target and targeted pathway information", Nucleic acids research, 44(D1), pp.D1069~D1074 (2016)
- Zarin, Deborah A, "The ClinicalTrials.gov results database—update and key issues", New England Journal of Medicine, 364(9), pp.852~860 (2011)
- Piñero, Janet, "DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants", Nucleic Acids Research, pp.gkw943~ (2016)
- Kanehisa, Minoru, "KEGG: new perspectives on genomes, pathways, diseases and drugs", Nucleic Acids Research, 45(D1), pp.D353~D361 (2017)
- "Genetics Home Reference"[URL]
- 김정우, "생물학 문헌 데이터의 제목과 본문을 이용한 질병 관련 유전자 추론 방법", 정보과학회 컴퓨팅의 실제 논문지, 23(1), pp.28~36 (2017), 한국정보과학회
- Butcher, J. C, "Random sampling from the normal distribution", The Computer Journal, 3(4), pp.251~253 (1961)
