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Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma

Mitochondrial dysfunction is common in cancer, and the mitochondrial electron transport chain is often affected in carcinogenesis. So far, few is known about the expression of the mitochondrial complex III (ubiquinol-cytochrome c reductase complex) subunits in clear cell renal cell carcinoma (ccRCC)...

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Autores principales: Ellinger, Jörg, Gromes, Arabella, Poss, Mirjam, Brüggemann, Maria, Schmidt, Doris, Ellinger, Nadja, Tolkach, Yuri, Dietrich, Dimo, Kristiansen, Glen, Müller, Stefan C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349929/
https://www.ncbi.nlm.nih.gov/pubmed/27845902
http://dx.doi.org/10.18632/oncotarget.13275
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author Ellinger, Jörg
Gromes, Arabella
Poss, Mirjam
Brüggemann, Maria
Schmidt, Doris
Ellinger, Nadja
Tolkach, Yuri
Dietrich, Dimo
Kristiansen, Glen
Müller, Stefan C.
author_facet Ellinger, Jörg
Gromes, Arabella
Poss, Mirjam
Brüggemann, Maria
Schmidt, Doris
Ellinger, Nadja
Tolkach, Yuri
Dietrich, Dimo
Kristiansen, Glen
Müller, Stefan C.
author_sort Ellinger, Jörg
collection PubMed
description Mitochondrial dysfunction is common in cancer, and the mitochondrial electron transport chain is often affected in carcinogenesis. So far, few is known about the expression of the mitochondrial complex III (ubiquinol-cytochrome c reductase complex) subunits in clear cell renal cell carcinoma (ccRCC). In this study, the NextBio database was used to determine an expression profile of the mitochondrial complex III subunits based on published microarray studies. We observed that five out of 11 subunits of the complex III were downregulated in at least three microarray studies. The decreased mRNA expression level of UQCRFS1 and UQCRC1 in ccRCC was confirmed using PCR. Low mRNA levels UQCRC1 were also correlated with a shorter period of cancer-specific and overall survival. Furthermore, UQCRFS1 and UQCRC1 were also decreased in ccRCC on the protein level as determined using Western blotting and immunohistochemistry. UQCRC1 protein expression was also lower in ccRCC than in papillary and chromophobe subtypes. Analyzing gene expression and DNA methylation in The Cancer Genome Atlas cohort revealed an inverse correlation of gene expression and DNA methylation, suggesting that DNA hypermethylation is regulating the expression of UQCRC1 and UQCRFS1. Taken together, our data implicate that dysregulated UQCRC1 and UQCRFS1 are involved in impaired mitochondrial electron transport chain function.
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spelling pubmed-53499292017-04-06 Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma Ellinger, Jörg Gromes, Arabella Poss, Mirjam Brüggemann, Maria Schmidt, Doris Ellinger, Nadja Tolkach, Yuri Dietrich, Dimo Kristiansen, Glen Müller, Stefan C. Oncotarget Research Paper Mitochondrial dysfunction is common in cancer, and the mitochondrial electron transport chain is often affected in carcinogenesis. So far, few is known about the expression of the mitochondrial complex III (ubiquinol-cytochrome c reductase complex) subunits in clear cell renal cell carcinoma (ccRCC). In this study, the NextBio database was used to determine an expression profile of the mitochondrial complex III subunits based on published microarray studies. We observed that five out of 11 subunits of the complex III were downregulated in at least three microarray studies. The decreased mRNA expression level of UQCRFS1 and UQCRC1 in ccRCC was confirmed using PCR. Low mRNA levels UQCRC1 were also correlated with a shorter period of cancer-specific and overall survival. Furthermore, UQCRFS1 and UQCRC1 were also decreased in ccRCC on the protein level as determined using Western blotting and immunohistochemistry. UQCRC1 protein expression was also lower in ccRCC than in papillary and chromophobe subtypes. Analyzing gene expression and DNA methylation in The Cancer Genome Atlas cohort revealed an inverse correlation of gene expression and DNA methylation, suggesting that DNA hypermethylation is regulating the expression of UQCRC1 and UQCRFS1. Taken together, our data implicate that dysregulated UQCRC1 and UQCRFS1 are involved in impaired mitochondrial electron transport chain function. Impact Journals LLC 2016-11-10 /pmc/articles/PMC5349929/ /pubmed/27845902 http://dx.doi.org/10.18632/oncotarget.13275 Text en Copyright: © 2016 Ellinger 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
Ellinger, Jörg
Gromes, Arabella
Poss, Mirjam
Brüggemann, Maria
Schmidt, Doris
Ellinger, Nadja
Tolkach, Yuri
Dietrich, Dimo
Kristiansen, Glen
Müller, Stefan C.
Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma
title Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma
title_full Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma
title_fullStr Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma
title_full_unstemmed Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma
title_short Systematic expression analysis of the mitochondrial complex III subunits identifies UQCRC1 as biomarker in clear cell renal cell carcinoma
title_sort systematic expression analysis of the mitochondrial complex iii subunits identifies uqcrc1 as biomarker in clear cell renal cell carcinoma
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5349929/
https://www.ncbi.nlm.nih.gov/pubmed/27845902
http://dx.doi.org/10.18632/oncotarget.13275
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