pone.0172955.g006.tif (1.01 MB)
Cytokine relationship with potential inflammatory effects in KD.
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posted on 2017-03-03, 18:34 authored by N. Jumper, T. Hodgkinson, R. Paus, A. BayatSchematic diagram of the possible relationships existing between a number of cytokines and growth factors identified as dysregulated in KD microdissected epidermis and dermis in our microarray data. This figure should be correlated with Table 2 where the direction and fold change for each of these molecules can be found for each site within keloid epidermis and dermis. AP-1, activating protein 1; IL, interleukin; INF, interferon; JAK, janus kinase; MMP, matrix metalloproteinase; NFκB, nuclear factor kappa B; ROR, retinoic acid-related orphan receptor c; STAT, signal transducer and activator of transcription; TGFβ, transforming growth factor beta; TNF, tumour necrosis factor.
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fibroproliferative cutaneous tumour characterisedmonolayer cell culture techniquesgene expressionkeloid lesional sitesapproachcharacterise expression differencesfuture explorative researchunravelling keloid disease pathobiology Keloid diseasefuture KD researchbetter-defined gene signaturesTGFmicrodissectionSite-specific gene expressioncollagen deposition
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