When this paper first published it contained a number of errors.
The data availability statement originally read “The RNA sequencing data are deposited in the NCBI GEO database. The accession number is GSE147145. The RNA sequencing data will be released in thepublic domain once the manuscript is accepted. For the reviewer's access, the token code is ixkvgeechdsbbyj. Any other raw data are available on reasonable request”. It should have read “The RNA sequencing data are deposited in the NCBI GEO database. The accession number is GSE147145. Any other raw data are available on reasonable request”.
The conflict of interest statement originally read “Done Statement.” It should have read “The authors declare that they do not have any conflict of interest”.
The figure 5 legend contained text that read “The hub proteins MAPK1/ERK2, MAPK3/ERK1 in the network are highlighted”. This should have read “The hub proteins MAPK1/ERK2, MAPK3/ERK1 in the network are encircled.”
These corrections have now been applied to the paper online.
Protein–protein interaction network analysis of the genes significantly (Padj < 0.1) upregulated upon miR-592 expression in D283 cells and the western blot analysis of the expression levels of proteins of the AKT signaling pathway. (A) The network is built from the genes significantly enriched (Padj < 0.01) in the pathways from the KEGG and Reactome databases without any additional interactors. Padj = P-value corrected by the Bonferroni step-down method. The hub proteins MAPK1/ERK2, MAPK3/ERK1 in the network are encircled (B) VC: vector control, P1, P2: populations expressing miR-592. The numbers below each blot indicate the fold change in the expression levels compared to VC after normalization using the housekeeping protein γ-tubulin levels or the corresponding total protein levels in the case of phosphorylated forms.
