Improved Candidate Drug Mining for Alzheimer's Disease

被引:2
|
作者
Cheng, Yu-Huei [1 ]
Chuang, Li-Yeh [2 ]
Chang, Hsueh-Wei [3 ,4 ,5 ,6 ]
Yang, Cheng-Hong [7 ]
机构
[1] Toko Univ, Dept Digital Content Design & Management, Chiayi 613, Taiwan
[2] I Shou Univ, Inst Biotechnol & Chem Engn, Dept Chem Engn, Kaohsiung 84001, Taiwan
[3] Kaohsiung Med Univ, Dept Biomed Sci & Environm Biol, Kaohsiung 80708, Taiwan
[4] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Translat Res Ctr, Kaohsiung 80708, Taiwan
[5] Kaohsiung Med Univ, Kaohsiung Med Univ Hosp, Ctr Canc, Kaohsiung 80708, Taiwan
[6] Natl Sun Yat Sen Univ, Inst Med Sci & Technol, Kaohsiung 80424, Taiwan
[7] Natl Kaohsiung Univ Appl Sci, Dept Elect Engn, Kaohsiung 80778, Taiwan
关键词
SINGLE-NUCLEOTIDE POLYMORPHISM; PRIMER DESIGN; SNP; DEMENTIA; ASSAY;
D O I
10.1155/2014/897653
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
Alzheimer's disease (AD) is the main cause of dementia for older people. Although several antidementia drugs such as donepezil, rivastigmine, galantamine, and memantine have been developed, the effectiveness of AD drug therapy is still far from satisfactory. Recently, the single nucleotide polymorphisms (SNPs) have been chosen as one of the personalized medicine markers. Many pharmacogenomics databases have been developed to provide comprehensive information by associating SNPs with drug responses, disease incidence, and genes that are critical in choosing personalized therapy. However, we found that some information from different sets of pharmacogenomics databases is not sufficient and this may limit the potential functions for pharmacogenomics. To address this problem, we used approximate string matching method and data mining approach to improve the searching of pharmacogenomics database. After computation, we can successfully identify more genes linked to AD and AD-related drugs than previous online searching. These improvements may help to improve the pharmacogenomics of AD for personalized medicine.
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页数:8
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