| Literature DB >> 28423655 |
Hong-Yan Lai1, Xin-Xin Chen1, Wei Chen1,2, Hua Tang3, Hao Lin1.
Abstract
Lectins are a diverse type of glycoproteins or carbohydrate-binding proteins that have a wide distribution to various species. They can specially identify and exclusively bind to a certain kind of saccharide groups. Cancerlectins are a group of lectins that are closely related to cancer and play a major role in the initiation, survival, growth, metastasis and spread of tumor. Several computational methods have emerged to discriminate cancerlectins from non-cancerlectins, which promote the study on pathogenic mechanisms and clinical treatment of cancer. However, the predictive accuracies of most of these techniques are very limited. In this work, by constructing a benchmark dataset based on the CancerLectinDB database, a new amino acid sequence-based strategy for feature description was developed, and then the binomial distribution was applied to screen the optimal feature set. Ultimately, an SVM-based predictor was performed to distinguish cancerlectins from non-cancerlectins, and achieved an accuracy of 77.48% with AUC of 85.52% in jackknife cross-validation. The results revealed that our prediction model could perform better comparing with published predictive tools.Entities:
Keywords: SVM; binomial distribution; cancerlectins; optimal tripeptides
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Year: 2017 PMID: 28423655 PMCID: PMC5438640 DOI: 10.18632/oncotarget.15963
Source DB: PubMed Journal: Oncotarget ISSN: 1949-2553