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. 2018 Mar 6;9:433. doi: 10.3389/fimmu.2018.00433

Table 1.

In silico pathway analysis of cellular miRNAs altered by v-miRs.

Viral miRNA (cell type) Predicted pathways
HSV1 miR-H1 [human oral keratinocytes (HOK)] Actin cytoskeleton
Calcium signaling
Focal adhesions
MAPK pathway
PI3K-Akt signaling pathway
Wnt pathway

KSHV K12-3p (HOK) Focal adhesions pathway
Adherens pathway
Actin cytoskeleton genes
MAPK signaling pathway
PI3K-Akt pathway

Human cytomegalovirus (HCMV) UL-70 (HOK) MAPK gene
Focal adhesions pathway
Gap junction genes
ERB pathway

HSV1 miR-H1 (Mφ) Calcium signaling pathways
Endocytosis pathway
MAPK signaling pathway
T cell receptor genes
Wnt signaling pathway
RNA transport genes
PI3K-Akt genes
TGF-β signaling pathway

KSHV K12-3p (Mφ) Endocytosis Pathway
MAPK Signaling Pathway
PIK-Akt Pathway
Protein Production in ER
RNA Transport Genes
Wnt Signaling Pathway

HCMV UL-70 (Mφ) Apoptosis
Chemokine
Endocytosis pathway
Erb pathway
Osteoclast differentiation pathways
PI3K-Akt pathway
T-cell receptor genes

Cellular miRNAs dysregulated by v-miRs in both HOK and Mφ were analyzed for the identification of cellular pathways. List of top 5–8 pathways are listed.