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RORα and RORγ expression inversely correlates with human melanoma progression
The retinoic acid-related orphan receptors (RORs) regulate several physiological and pathological processes, including immune functions, development and cancer. To study the potential role of RORs in melanoma progression, we analysed RORα and RORγ expression in nevi and primary melanomas and non-les...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325362/ https://www.ncbi.nlm.nih.gov/pubmed/27542227 http://dx.doi.org/10.18632/oncotarget.11211 |
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author | Brożyna, Anna A. Jóźwicki, Wojciech Skobowiat, Cezary Jetten, Anton Slominski, Andrzej T. |
author_facet | Brożyna, Anna A. Jóźwicki, Wojciech Skobowiat, Cezary Jetten, Anton Slominski, Andrzej T. |
author_sort | Brożyna, Anna A. |
collection | PubMed |
description | The retinoic acid-related orphan receptors (RORs) regulate several physiological and pathological processes, including immune functions, development and cancer. To study the potential role of RORs in melanoma progression, we analysed RORα and RORγ expression in nevi and primary melanomas and non-lesional skin and metastases in relation to melanoma clinico-pathomorphological features. The expression of RORα and RORγ was lower in melanomas than in nevi and decreased during melanoma progression, with lowest levels found in primary melanomas at stages III and IV and in melanoma metastases. Their expression correlated with pathomorphological pTNM parameters being low in aggressive tumors and being high in tumors showing histological markers of good prognosis. Higher nuclear levels of RORα and RORγ and of cytoplasmic RORγ correlated with significantly longer overall and disease free survival time. Highly pigmented melanomas showed significantly lower level of nuclear RORs. This study shows that human melanoma development and aggressiveness is associated with decreased expression of RORα and RORγ, suggesting that RORs could be important in melanoma progression and host responses against the tumor. Furthermore, it suggests that RORα and RORγ might constitute a novel druggable target in anti-melanoma management using tumor suppressor gene therapy restoring their normal functions. |
format | Online Article Text |
id | pubmed-5325362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53253622017-03-10 RORα and RORγ expression inversely correlates with human melanoma progression Brożyna, Anna A. Jóźwicki, Wojciech Skobowiat, Cezary Jetten, Anton Slominski, Andrzej T. Oncotarget Research Paper The retinoic acid-related orphan receptors (RORs) regulate several physiological and pathological processes, including immune functions, development and cancer. To study the potential role of RORs in melanoma progression, we analysed RORα and RORγ expression in nevi and primary melanomas and non-lesional skin and metastases in relation to melanoma clinico-pathomorphological features. The expression of RORα and RORγ was lower in melanomas than in nevi and decreased during melanoma progression, with lowest levels found in primary melanomas at stages III and IV and in melanoma metastases. Their expression correlated with pathomorphological pTNM parameters being low in aggressive tumors and being high in tumors showing histological markers of good prognosis. Higher nuclear levels of RORα and RORγ and of cytoplasmic RORγ correlated with significantly longer overall and disease free survival time. Highly pigmented melanomas showed significantly lower level of nuclear RORs. This study shows that human melanoma development and aggressiveness is associated with decreased expression of RORα and RORγ, suggesting that RORs could be important in melanoma progression and host responses against the tumor. Furthermore, it suggests that RORα and RORγ might constitute a novel druggable target in anti-melanoma management using tumor suppressor gene therapy restoring their normal functions. Impact Journals LLC 2016-08-11 /pmc/articles/PMC5325362/ /pubmed/27542227 http://dx.doi.org/10.18632/oncotarget.11211 Text en Copyright: © 2016 Brożyna et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Brożyna, Anna A. Jóźwicki, Wojciech Skobowiat, Cezary Jetten, Anton Slominski, Andrzej T. RORα and RORγ expression inversely correlates with human melanoma progression |
title | RORα and RORγ expression inversely correlates with human melanoma progression |
title_full | RORα and RORγ expression inversely correlates with human melanoma progression |
title_fullStr | RORα and RORγ expression inversely correlates with human melanoma progression |
title_full_unstemmed | RORα and RORγ expression inversely correlates with human melanoma progression |
title_short | RORα and RORγ expression inversely correlates with human melanoma progression |
title_sort | rorα and rorγ expression inversely correlates with human melanoma progression |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5325362/ https://www.ncbi.nlm.nih.gov/pubmed/27542227 http://dx.doi.org/10.18632/oncotarget.11211 |
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