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. 2013 Dec 10;46(4):113–122. doi: 10.1152/physiolgenomics.00157.2013

Table 2.

miRNAs that express aberrantly in human psoriatic skin and relative amount of their companion 5′-isomiRs

miRNA Description Fold Change (PP/NN) IsomiRs, %
miR-31 regulates cytokine/chemokine expression via targeting serine/threonine kinase 40 (STK40) 42.9 0.4
miR-977 mirtron; upregulated in psoriatic skin 6.4 1.3
miR-135b/miR-7 targets late cornified envelope-1B (LCE1B); impairs barrier development and response to environmental stimuli 5.6/3.1 0.4/1.0
miR-1983 tRNA-derived human homolog of murine miR-1983 4.9 0.2
miR-21 contributes to T cell-derived psoriatic skin inflammation 4.0 0.6
miR-203-AS antisense to miR-203 2.7 7
miR-155/miR-142/miR-146a cell fate decisions in hematopoietic development 2.7/2.5/2.3 1.1/46/0.8
miR-223 suppresses cell proliferation by targeting IGF-1R 2.5 9.8
miR-203 regulates the transition from basal to suprabasal layer in epidermis 1.6 43
miR-205 primarily in the basal layer expressed in normal skin and regulates the transcriptional repressor of E-cadherin to maintain epithelial-mesenchymal transition 1.6 0.5
miR-99a/miR-100 inhibits angiogenesis by repressing the mammalian target of rapamycin (mTOR) in endothelial cells −2.1/−2.3 3.1/0.7
mir-10a regulates the behavior of endothelial cells during angiogenesis −2.3 22
miR-124 downregulation in skin cancer, cutaneous squamous cells −5.9 23
miR-4490 novel miRNA from intergenic region −8.1 1.2

Fold change is a value of miRNA expression in psoriatic skin (PP) divided by that in normal skin (NN). IsomiRs, the percentage of reads mapping to miRNA hairpins identified as 5′-isomiRs.