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. 2018 Jul 19;16(4):4159–4168. doi: 10.3892/ol.2018.9175

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Copyright: © Liang et al.

This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.

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Figure 1. — Process of analysis of the present study. By comparing previously published sequencing results of BC miRNAs, a total of 6 miRNAs supported by multiple datasets were identified. Then the target genes regulated by these meta-miRNAs were predicted. The meta-miRNAs functions on pathogenesis of breast cancer were enriched through functional enrichment analysis of the target genes of the meta-miRNAs, and transcription factor binding analysis. The numbers in brackets represent the number of processes, miRNAs or genes obtained by analysis. miRNA, microRNA; BC, breast cancer; DAVID, Database for Annotation, Visualization and Integrated Discovery; TF, transcription factor.