Comprehensive Proteomic Analysis Reveals Intermediate Stage of Non-Lesional Psoriatic Skin and Points out the Importance of Proteins Outside this Trend
To better understand the pathomechanism of psoriasis, a comparative proteomic analysis was performed with non-lesional and lesional skin from psoriasis patients and skin from healthy individuals. Strikingly, 79.9% of the proteins that were differentially expressed in lesional and healthy skin exhibi...
Elmentve itt :
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| Dokumentumtípus: | Cikk |
| Megjelent: |
2019
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| Sorozat: | SCIENTIFIC REPORTS
9 |
| doi: | 10.1038/s41598-019-47774-5 |
| mtmt: | 30774067 |
| Online Access: | http://publicatio.bibl.u-szeged.hu/17446 |
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| 245 | 1 | 0 | |a Comprehensive Proteomic Analysis Reveals Intermediate Stage of Non-Lesional Psoriatic Skin and Points out the Importance of Proteins Outside this Trend |h [elektronikus dokumentum] / |c Szél Edit |
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| 490 | 0 | |a SCIENTIFIC REPORTS |v 9 | |
| 520 | 3 | |a To better understand the pathomechanism of psoriasis, a comparative proteomic analysis was performed with non-lesional and lesional skin from psoriasis patients and skin from healthy individuals. Strikingly, 79.9% of the proteins that were differentially expressed in lesional and healthy skin exhibited expression levels in non-lesional skin that were within twofold of the levels observed in healthy and lesional skin, suggesting that non-lesional skin represents an intermediate stage. Proteins outside this trend were categorized into three groups: I. proteins in non-lesional skin exhibiting expression similar to lesional skin, which might be predisposing factors (i.e., CSE1L, GART, MYO18A and UGDH); II. proteins that were differentially expressed in non-lesional and lesional skin but not in healthy and lesional skin, which might be non-lesional characteristic alteration (i.e., CHCHD6, CHMP5, FLOT2, ITGA7, LEMD2, NOP56, PLVAP and RRAS); and III. proteins with contrasting differential expression in non-lesional and lesional skin compared to healthy skin, which might contribute to maintaining the non-lesional state (i.e., ITGA7, ITGA8, PLVAP, PSAPL1, SMARCA5 and XP32). Finally, proteins differentially expressed in lesions may indicate increased sensitivity to stimuli, peripheral nervous system alterations, furthermore MYBBP1A and PRKDC were identified as potential regulators of key pathomechanisms, including stress and immune response, proliferation and differentiation. | |
| 700 | 0 | 1 | |a Bozó Renáta |e aut |
| 700 | 0 | 2 | |a Hunyadi-Gulyás Éva Csilla |e aut |
| 700 | 0 | 2 | |a Manczinger Máté |e aut |
| 700 | 0 | 2 | |a Szabó Kornélia Ágnes |e aut |
| 700 | 0 | 2 | |a Kemény Lajos |e aut |
| 700 | 0 | 2 | |a Csörgő Sándorné Bata Zsuzsanna |e aut |
| 700 | 0 | 2 | |a Groma Gergely |e aut |
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