Cargando…

ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1

Autophagy is a highly conserved cellular process in which intracellular proteins and organelles are sequestered and degraded after the fusion of double-membrane vesicles known as autophagosomes with lysosomes. The process of autophagy is dependent on autophagy-related (ATG) proteins. The role of aut...

Descripción completa

Detalles Bibliográficos
Autores principales: Frangež, Živa, Gérard, Deborah, He, Zhaoyue, Gavriil, Marios, Fernández-Marrero, Yuniel, Seyed Jafari, S. Morteza, Hunger, Robert E., Lucarelli, Philippe, Yousefi, Shida, Sauter, Thomas, Sinkkonen, Lasse, Simon, Hans-Uwe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397460/
https://www.ncbi.nlm.nih.gov/pubmed/34458153
http://dx.doi.org/10.3389/fonc.2021.721624
_version_ 1783744620578996224
author Frangež, Živa
Gérard, Deborah
He, Zhaoyue
Gavriil, Marios
Fernández-Marrero, Yuniel
Seyed Jafari, S. Morteza
Hunger, Robert E.
Lucarelli, Philippe
Yousefi, Shida
Sauter, Thomas
Sinkkonen, Lasse
Simon, Hans-Uwe
author_facet Frangež, Živa
Gérard, Deborah
He, Zhaoyue
Gavriil, Marios
Fernández-Marrero, Yuniel
Seyed Jafari, S. Morteza
Hunger, Robert E.
Lucarelli, Philippe
Yousefi, Shida
Sauter, Thomas
Sinkkonen, Lasse
Simon, Hans-Uwe
author_sort Frangež, Živa
collection PubMed
description Autophagy is a highly conserved cellular process in which intracellular proteins and organelles are sequestered and degraded after the fusion of double-membrane vesicles known as autophagosomes with lysosomes. The process of autophagy is dependent on autophagy-related (ATG) proteins. The role of autophagy in cancer is very complex and still elusive. We investigated the expression of ATG proteins in benign nevi, primary and metastatic melanoma tissues using customized tissue microarrays (TMA). Results from immunohistochemistry show that the expression of ATG5 and ATG7 is significantly reduced in melanoma tissues compared to benign nevi. This reduction correlated with changes in the expression of autophagic activity markers, suggesting decreased basal levels of autophagy in primary and metastatic melanomas. Furthermore, the analysis of survival data of melanoma patients revealed an association between reduced ATG5 and ATG7 levels with an unfavourable clinical outcome. Currently, the mechanisms regulating ATG expression levels in human melanoma remains unknown. Using bioinformatic predictions of transcription factor (TF) binding motifs in accessible chromatin of primary melanocytes, we identified new TFs involved in the regulation of core ATGs. We then show that nuclear respiratory factor 1 (NRF1) stimulates the production of mRNA and protein as well as the promoter activity of ATG5 and ATG7. Moreover, NRF1 deficiency increased in vitro migration of melanoma cells. Our results support the concept that reduced autophagic activity contributes to melanoma development and progression, and identifies NRF1 as a novel TF involved in the regulation of both ATG5 and ATG7 genes.
format Online
Article
Text
id pubmed-8397460
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-83974602021-08-28 ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1 Frangež, Živa Gérard, Deborah He, Zhaoyue Gavriil, Marios Fernández-Marrero, Yuniel Seyed Jafari, S. Morteza Hunger, Robert E. Lucarelli, Philippe Yousefi, Shida Sauter, Thomas Sinkkonen, Lasse Simon, Hans-Uwe Front Oncol Oncology Autophagy is a highly conserved cellular process in which intracellular proteins and organelles are sequestered and degraded after the fusion of double-membrane vesicles known as autophagosomes with lysosomes. The process of autophagy is dependent on autophagy-related (ATG) proteins. The role of autophagy in cancer is very complex and still elusive. We investigated the expression of ATG proteins in benign nevi, primary and metastatic melanoma tissues using customized tissue microarrays (TMA). Results from immunohistochemistry show that the expression of ATG5 and ATG7 is significantly reduced in melanoma tissues compared to benign nevi. This reduction correlated with changes in the expression of autophagic activity markers, suggesting decreased basal levels of autophagy in primary and metastatic melanomas. Furthermore, the analysis of survival data of melanoma patients revealed an association between reduced ATG5 and ATG7 levels with an unfavourable clinical outcome. Currently, the mechanisms regulating ATG expression levels in human melanoma remains unknown. Using bioinformatic predictions of transcription factor (TF) binding motifs in accessible chromatin of primary melanocytes, we identified new TFs involved in the regulation of core ATGs. We then show that nuclear respiratory factor 1 (NRF1) stimulates the production of mRNA and protein as well as the promoter activity of ATG5 and ATG7. Moreover, NRF1 deficiency increased in vitro migration of melanoma cells. Our results support the concept that reduced autophagic activity contributes to melanoma development and progression, and identifies NRF1 as a novel TF involved in the regulation of both ATG5 and ATG7 genes. Frontiers Media S.A. 2021-08-12 /pmc/articles/PMC8397460/ /pubmed/34458153 http://dx.doi.org/10.3389/fonc.2021.721624 Text en Copyright © 2021 Frangež, Gérard, He, Gavriil, Fernández-Marrero, Seyed Jafari, Hunger, Lucarelli, Yousefi, Sauter, Sinkkonen and Simon https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Frangež, Živa
Gérard, Deborah
He, Zhaoyue
Gavriil, Marios
Fernández-Marrero, Yuniel
Seyed Jafari, S. Morteza
Hunger, Robert E.
Lucarelli, Philippe
Yousefi, Shida
Sauter, Thomas
Sinkkonen, Lasse
Simon, Hans-Uwe
ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1
title ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1
title_full ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1
title_fullStr ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1
title_full_unstemmed ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1
title_short ATG5 and ATG7 Expression Levels Are Reduced in Cutaneous Melanoma and Regulated by NRF1
title_sort atg5 and atg7 expression levels are reduced in cutaneous melanoma and regulated by nrf1
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8397460/
https://www.ncbi.nlm.nih.gov/pubmed/34458153
http://dx.doi.org/10.3389/fonc.2021.721624
work_keys_str_mv AT frangezziva atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT gerarddeborah atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT hezhaoyue atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT gavriilmarios atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT fernandezmarreroyuniel atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT seyedjafarismorteza atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT hungerroberte atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT lucarelliphilippe atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT yousefishida atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT sauterthomas atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT sinkkonenlasse atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1
AT simonhansuwe atg5andatg7expressionlevelsarereducedincutaneousmelanomaandregulatedbynrf1