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Identification of Chemical-Disease Associations Through Integration of Molecular Fingerprint, Gene Ontology and Pathway Information.
Li, Zhanchao; Wang, Mengru; Peng, Dongdong; Liu, Jie; Xie, Yun; Dai, Zong; Zou, Xiaoyong.
Affiliation
  • Li Z; School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou, 510006, People's Republic of China. zhanchao8052@gdpu.edu.cn.
  • Wang M; NMPA Key Laboratory for Technology Research and Evaluation of Pharmacovigilance, Guangzhou, 510006, People's Republic of China. zhanchao8052@gdpu.edu.cn.
  • Peng D; Key Laboratory of Digital Quality Evaluation of Chinese Materia Medica of State Administration of Traditional Chinese Medicine, Guangzhou, 510006, People's Republic of China. zhanchao8052@gdpu.edu.cn.
  • Liu J; School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou, 510006, People's Republic of China.
  • Xie Y; School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou, 510006, People's Republic of China.
  • Dai Z; School of Chemistry and Chemical Engineering, Guangdong Pharmaceutical University, Guangzhou, 510006, People's Republic of China.
  • Zou X; HuiZhou University, Huizhou, 516007, People's Republic of China.
Interdiscip Sci ; 14(3): 683-696, 2022 Sep.
Article in En | MEDLINE | ID: mdl-35391615
ABSTRACT
The identification of chemical-disease association types is helpful not only to discovery lead compounds and study drug repositioning, but also to treat disease and decipher pathomechanism. It is very urgent to develop computational method for identifying potential chemical-disease association types, since wet methods are usually expensive, laborious and time-consuming. In this study, molecular fingerprint, gene ontology and pathway are utilized to characterize chemicals and diseases. A novel predictor is proposed to recognize potential chemical-disease associations at the first layer, and further distinguish whether their relationships belong to biomarker or therapeutic relations at the second layer. The prediction performance of current method is assessed using the benchmark dataset based on ten-fold cross-validation. The practical prediction accuracies of the first layer and the second layer are 78.47% and 72.07%, respectively. The recognition ability for lead compounds, new drug indications, potential and true chemical-disease association pairs has also been investigated and confirmed by constructing a variety of datasets and performing a series of experiments. It is anticipated that the current method can be considered as a powerful high-throughput virtual screening tool for drug researches and developments.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Repositioning Type of study: Diagnostic_studies / Risk_factors_studies Language: En Journal: Interdiscip Sci Journal subject: BIOLOGIA Year: 2022 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Drug Repositioning Type of study: Diagnostic_studies / Risk_factors_studies Language: En Journal: Interdiscip Sci Journal subject: BIOLOGIA Year: 2022 Document type: Article