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In recent studies, non-coding protein RNAs have been identified as microRNA that can be used as biomarkers for early diagnosis and treatment of cancer, that decrease mortality in cancer. A microRNA may target hundreds or thousands of genes and a gene may regulate several microRNAs, so determining which microRNA is associated with which cancer is a big challenge. Many computational methods have been performed to detect micoRNAs association with cancer, but more effort is needed with higher accuracy. Increasing research has shown that relationship between microRNAs and TFs play a significant role in the diagnosis of cancer. Therefore, we developed a new computational framework (CAMIRADA) to identify cancer-related microRNAs based on the relationship between microRNAs and disease genes (DG) in the protein network, the functional relationships between microRNAs and Transcription Factors (TF) on the co-expression network, and the relationship between microRNAs and the Differential Expression Gene (DEG) on co-expression network. The CAMIRADA was applied to assess breast cancer data from two HMDD and miR2Disease databases. In this study, the AUC for the 65 microRNAs of the top of the list was 0.95, which was more accurate than the similar methods used to detect microRNAs associated with the cancer artery. |
