A proteomic analysis of an in vitro knock-out of miR-200c

Abstract Loss of miR-200c is correlated to advanced cancer-subtypes due to increased EMT and decreased treatment efficacy by chemotherapeutics. As miRNAs regulate a multitude of targets, the analysis of differentially expressed proteins upon a genomic knock-out (KO) is of interest. In this study, we...

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Autores principales: Bojan Ljepoja, Jonathan García-Roman, Ann-Katrin Sommer, Thomas Fröhlich, Georg J. Arnold, Ernst Wagner, Andreas Roidl
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Publicado: Nature Portfolio 2018
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spelling oai:doaj.org-article:33c8ee14553a400c8741f1a8882b09952021-12-02T12:32:35ZA proteomic analysis of an in vitro knock-out of miR-200c10.1038/s41598-018-25240-y2045-2322https://doaj.org/article/33c8ee14553a400c8741f1a8882b09952018-05-01T00:00:00Zhttps://doi.org/10.1038/s41598-018-25240-yhttps://doaj.org/toc/2045-2322Abstract Loss of miR-200c is correlated to advanced cancer-subtypes due to increased EMT and decreased treatment efficacy by chemotherapeutics. As miRNAs regulate a multitude of targets, the analysis of differentially expressed proteins upon a genomic knock-out (KO) is of interest. In this study, we generated a TALENs KO of miR-200c in MCF7 breast cancer cells, excluded its compensation by family-members and evaluated the impact on the proteome by analyzing three individual KO-clones. We identified 26 key proteins and a variety of enrichments in metabolic and cytoskeletal pathways. In six of these targets (AGR2, FLNA/B, ALDH7A1, SCIN, GSTM3) the differential expression was additionally detected at mRNA level. Together, these alterations in protein abundance accounted for the observed biological phenotypes, i.e. increased migration and chemoresistance and altered metabolism, found in the miR-200c-KO clones. These findings provide novel insights into miR-200c and pave the way for further studies.Bojan LjepojaJonathan García-RomanAnn-Katrin SommerThomas FröhlichGeorg J. ArnoldErnst WagnerAndreas RoidlNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 8, Iss 1, Pp 1-15 (2018)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Bojan Ljepoja
Jonathan García-Roman
Ann-Katrin Sommer
Thomas Fröhlich
Georg J. Arnold
Ernst Wagner
Andreas Roidl
A proteomic analysis of an in vitro knock-out of miR-200c
description Abstract Loss of miR-200c is correlated to advanced cancer-subtypes due to increased EMT and decreased treatment efficacy by chemotherapeutics. As miRNAs regulate a multitude of targets, the analysis of differentially expressed proteins upon a genomic knock-out (KO) is of interest. In this study, we generated a TALENs KO of miR-200c in MCF7 breast cancer cells, excluded its compensation by family-members and evaluated the impact on the proteome by analyzing three individual KO-clones. We identified 26 key proteins and a variety of enrichments in metabolic and cytoskeletal pathways. In six of these targets (AGR2, FLNA/B, ALDH7A1, SCIN, GSTM3) the differential expression was additionally detected at mRNA level. Together, these alterations in protein abundance accounted for the observed biological phenotypes, i.e. increased migration and chemoresistance and altered metabolism, found in the miR-200c-KO clones. These findings provide novel insights into miR-200c and pave the way for further studies.
format article
author Bojan Ljepoja
Jonathan García-Roman
Ann-Katrin Sommer
Thomas Fröhlich
Georg J. Arnold
Ernst Wagner
Andreas Roidl
author_facet Bojan Ljepoja
Jonathan García-Roman
Ann-Katrin Sommer
Thomas Fröhlich
Georg J. Arnold
Ernst Wagner
Andreas Roidl
author_sort Bojan Ljepoja
title A proteomic analysis of an in vitro knock-out of miR-200c
title_short A proteomic analysis of an in vitro knock-out of miR-200c
title_full A proteomic analysis of an in vitro knock-out of miR-200c
title_fullStr A proteomic analysis of an in vitro knock-out of miR-200c
title_full_unstemmed A proteomic analysis of an in vitro knock-out of miR-200c
title_sort proteomic analysis of an in vitro knock-out of mir-200c
publisher Nature Portfolio
publishDate 2018
url https://doaj.org/article/33c8ee14553a400c8741f1a8882b0995
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