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The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data

The KRAB‐ZNF (Krüppel‐associated box domain zinc finger) gene family is composed of a large number of highly homologous genes, gene isoforms, and pseudogenes. The proteins encoded by these genes, whose expression is often tissue‐specific, act as epigenetic suppressors contributing to the addition of...

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Autores principales: Machnik, Marta, Cylwa, Rafał, Kiełczewski, Kornel, Biecek, Przemysław, Liloglou, Triantafillos, Mackiewicz, Andrzej, Oleksiewicz, Urszula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442004/
https://www.ncbi.nlm.nih.gov/pubmed/30444046
http://dx.doi.org/10.1002/1878-0261.12407
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author Machnik, Marta
Cylwa, Rafał
Kiełczewski, Kornel
Biecek, Przemysław
Liloglou, Triantafillos
Mackiewicz, Andrzej
Oleksiewicz, Urszula
author_facet Machnik, Marta
Cylwa, Rafał
Kiełczewski, Kornel
Biecek, Przemysław
Liloglou, Triantafillos
Mackiewicz, Andrzej
Oleksiewicz, Urszula
author_sort Machnik, Marta
collection PubMed
description The KRAB‐ZNF (Krüppel‐associated box domain zinc finger) gene family is composed of a large number of highly homologous genes, gene isoforms, and pseudogenes. The proteins encoded by these genes, whose expression is often tissue‐specific, act as epigenetic suppressors contributing to the addition of repressive chromatin marks and DNA methylation. Due to its high complexity, the KRAB‐ZNF family has not been studied in sufficient detail, and the involvement of its members in carcinogenesis remains mostly unexplored. In this study, we aimed to provide a comprehensive description of cancer‐associated KRAB‐ZNFs using publicly available The Cancer Genome Atlas pan‐cancer datasets. We analyzed 6727 tumor and normal tissue samples from 16 cancer types. Here, we showed that a small but distinctive cluster of 16 KRAB‐ZNFs is commonly upregulated across multiple cancer cohorts in comparison to normal samples. We confirmed these observations in the independent panels of lung and breast cancer cell lines and tissues. This upregulation was also observed for most of the KRAB‐ZNF splicing variants, whose expression is simultaneously upregulated in tumors compared to normal tissues. Finally, by analyzing the clinicopathological data for breast and lung cancers, we demonstrated that the expression of cancer‐associated KRAB‐ZNFs correlates with patient survival, tumor histology, and molecular subtyping. Altogether, our study allowed the identification and characterization of KRAB‐ZNF factors that may have an essential function in cancer biology and thus potential to become novel oncologic biomarkers and treatment targets.
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spelling pubmed-64420042019-04-11 The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data Machnik, Marta Cylwa, Rafał Kiełczewski, Kornel Biecek, Przemysław Liloglou, Triantafillos Mackiewicz, Andrzej Oleksiewicz, Urszula Mol Oncol Research Articles The KRAB‐ZNF (Krüppel‐associated box domain zinc finger) gene family is composed of a large number of highly homologous genes, gene isoforms, and pseudogenes. The proteins encoded by these genes, whose expression is often tissue‐specific, act as epigenetic suppressors contributing to the addition of repressive chromatin marks and DNA methylation. Due to its high complexity, the KRAB‐ZNF family has not been studied in sufficient detail, and the involvement of its members in carcinogenesis remains mostly unexplored. In this study, we aimed to provide a comprehensive description of cancer‐associated KRAB‐ZNFs using publicly available The Cancer Genome Atlas pan‐cancer datasets. We analyzed 6727 tumor and normal tissue samples from 16 cancer types. Here, we showed that a small but distinctive cluster of 16 KRAB‐ZNFs is commonly upregulated across multiple cancer cohorts in comparison to normal samples. We confirmed these observations in the independent panels of lung and breast cancer cell lines and tissues. This upregulation was also observed for most of the KRAB‐ZNF splicing variants, whose expression is simultaneously upregulated in tumors compared to normal tissues. Finally, by analyzing the clinicopathological data for breast and lung cancers, we demonstrated that the expression of cancer‐associated KRAB‐ZNFs correlates with patient survival, tumor histology, and molecular subtyping. Altogether, our study allowed the identification and characterization of KRAB‐ZNF factors that may have an essential function in cancer biology and thus potential to become novel oncologic biomarkers and treatment targets. John Wiley and Sons Inc. 2019-02-16 2019-04 /pmc/articles/PMC6442004/ /pubmed/30444046 http://dx.doi.org/10.1002/1878-0261.12407 Text en © 2018 The Authors. Published by FEBS Press and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Machnik, Marta
Cylwa, Rafał
Kiełczewski, Kornel
Biecek, Przemysław
Liloglou, Triantafillos
Mackiewicz, Andrzej
Oleksiewicz, Urszula
The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data
title The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data
title_full The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data
title_fullStr The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data
title_full_unstemmed The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data
title_short The expression signature of cancer‐associated KRAB‐ZNF factors identified in TCGA pan‐cancer transcriptomic data
title_sort expression signature of cancer‐associated krab‐znf factors identified in tcga pan‐cancer transcriptomic data
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6442004/
https://www.ncbi.nlm.nih.gov/pubmed/30444046
http://dx.doi.org/10.1002/1878-0261.12407
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