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...
Guardado en:
Autores principales: | , , , , , , |
---|---|
Formato: | article |
Lenguaje: | EN |
Publicado: |
Nature Portfolio
2018
|
Materias: | |
Acceso en línea: | https://doaj.org/article/33c8ee14553a400c8741f1a8882b0995 |
Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|
id |
oai:doaj.org-article:33c8ee14553a400c8741f1a8882b0995 |
---|---|
record_format |
dspace |
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 |
work_keys_str_mv |
AT bojanljepoja aproteomicanalysisofaninvitroknockoutofmir200c AT jonathangarciaroman aproteomicanalysisofaninvitroknockoutofmir200c AT annkatrinsommer aproteomicanalysisofaninvitroknockoutofmir200c AT thomasfrohlich aproteomicanalysisofaninvitroknockoutofmir200c AT georgjarnold aproteomicanalysisofaninvitroknockoutofmir200c AT ernstwagner aproteomicanalysisofaninvitroknockoutofmir200c AT andreasroidl aproteomicanalysisofaninvitroknockoutofmir200c AT bojanljepoja proteomicanalysisofaninvitroknockoutofmir200c AT jonathangarciaroman proteomicanalysisofaninvitroknockoutofmir200c AT annkatrinsommer proteomicanalysisofaninvitroknockoutofmir200c AT thomasfrohlich proteomicanalysisofaninvitroknockoutofmir200c AT georgjarnold proteomicanalysisofaninvitroknockoutofmir200c AT ernstwagner proteomicanalysisofaninvitroknockoutofmir200c AT andreasroidl proteomicanalysisofaninvitroknockoutofmir200c |
_version_ |
1718394029958234112 |