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Gene expression analysis of melanocortin system in vitiligo

Kingo, K., Aunin, E., Karelson, M., Philips, M-A, Rätsep, R., Silm, H., Vasar, E., Soomets, U. and Kõks, S. (2007) Gene expression analysis of melanocortin system in vitiligo. Journal of Dermatological Science, 48 (2). pp. 113-122.

Link to Published Version: https://doi.org/10.1016/j.jdermsci.2007.06.004
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Abstract

Background
The melanocortin system in the skin coordinates pigmentation and immune response and could be implicated in the pathogenesis of vitiligo.

Objectives
We aimed to analyze changes in expression of genes involved in skin pigmentation (melanocortin system and enzymes involved in melanin synthesis).

Methods
With quantitative RT-PCR we measured the mRNA expression levels of eight genes from the melanocortin system and two enzymes involved in melanogenesis. RNA was extracted from both lesional and non-lesional skin of vitiligo patients and in non-sun-exposed skin of healthy subjects.

Results
POMC (proopiomelanocortin) expression was lower in lesional skin compared to non-lesional skin. Expression of melanocortin receptors was increased in unaffected skin of vitiligo patients compared to healthy subjects and decreased in lesional skin compared to uninvolved skin of vitiligo patients, the differences were statistically significant in the cases of MC1R (melanocortin receptor 1) and MC4R (melanocortin receptor 4). TRP1 and DCT genes were down-regulated in lesional skin compared to non-lesional vitiligo skin or skin of healthy controls and up-regulated in uninvolved vitiligo skin compared to healthy control samples. In non-lesional skin, POMC expression was not elevated, possibly indicating that systemic influences are involved in up-regulation of MC receptor genes. Decreased expression of the analyzed genes in the lesional skin is not surprising, but statistically significant increased expression of studied genes in non-lesional skin from vitiligo patients is not described previously.

Conclusion
In our mind, up-regulation of melanocortin system in non-lesional skin could be systemic compensation to restore normal pigmentation in lesions.

Item Type: Journal Article
Publisher: Elsevier Ireland Ltd
Copyright: © 2007 Japanese Society for Investigative Dermatology
URI: http://researchrepository.murdoch.edu.au/id/eprint/52776
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