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The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy

The Mediator complex, a multi-subunit protein complex, plays an integral role in regulating transcription. Genetic alterations of the mediator subunit 15 (MED15) in separate tumor entities have been described previously. However, till now, not much is known about the role of MED15 in urothelial blad...

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Autores principales: Syring, Isabella, Weiten, Richard, Müller, Tim, Schmidt, Doris, Steiner, Susanne, Kristiansen, Glen, Müller, Stefan C., Ellinger, Jörg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096071/
https://www.ncbi.nlm.nih.gov/pubmed/30127891
http://dx.doi.org/10.3892/ol.2018.9014
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author Syring, Isabella
Weiten, Richard
Müller, Tim
Schmidt, Doris
Steiner, Susanne
Kristiansen, Glen
Müller, Stefan C.
Ellinger, Jörg
author_facet Syring, Isabella
Weiten, Richard
Müller, Tim
Schmidt, Doris
Steiner, Susanne
Kristiansen, Glen
Müller, Stefan C.
Ellinger, Jörg
author_sort Syring, Isabella
collection PubMed
description The Mediator complex, a multi-subunit protein complex, plays an integral role in regulating transcription. Genetic alterations of the mediator subunit 15 (MED15) in separate tumor entities have been described previously. However, till now, not much is known about the role of MED15 in urothelial bladder cancer (BCa). Using cBioPortal, database analysis was executed for the mRNA expression and survival analysis of MED15 in BCa. Immunohistochemistry (IHC) analysis against MED15 was performed on tissue microarrays with 18 benign, 126 BCa, and 38 metastases samples. The intensity evaluation was performed using a staining intensity score from 0 to 3 and associated with clinicopathological data. The BCa cell lines T24 and TCCSUP were used for the functional investigation. After the MED15 knockdown by small interfering (si)RNA, cell proliferation, migration and invasion were investigated. On the mRNA level, only a low number of alterations (2%) was found for MED15 in BCa. Due to the small count of events, there were no significant differences or tendencies in survival. For IHC, MED15 was found to have a higher expression in non-muscle invasive BCa compared with benign and muscle invasive BCa. For survival analysis, no significant differences between samples with or without overexpression of MED15 were found. In the functional analysis, proliferation, migration, and invasion were significantly reduced in BCa-cells following the transient siRNA-mediated MED15 knockdown. In summary, MED15 appears to play a role in the tumor parameters proliferation, migration, and invasion in BCa, but further investigations are necessary.
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spelling pubmed-60960712018-08-20 The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy Syring, Isabella Weiten, Richard Müller, Tim Schmidt, Doris Steiner, Susanne Kristiansen, Glen Müller, Stefan C. Ellinger, Jörg Oncol Lett Articles The Mediator complex, a multi-subunit protein complex, plays an integral role in regulating transcription. Genetic alterations of the mediator subunit 15 (MED15) in separate tumor entities have been described previously. However, till now, not much is known about the role of MED15 in urothelial bladder cancer (BCa). Using cBioPortal, database analysis was executed for the mRNA expression and survival analysis of MED15 in BCa. Immunohistochemistry (IHC) analysis against MED15 was performed on tissue microarrays with 18 benign, 126 BCa, and 38 metastases samples. The intensity evaluation was performed using a staining intensity score from 0 to 3 and associated with clinicopathological data. The BCa cell lines T24 and TCCSUP were used for the functional investigation. After the MED15 knockdown by small interfering (si)RNA, cell proliferation, migration and invasion were investigated. On the mRNA level, only a low number of alterations (2%) was found for MED15 in BCa. Due to the small count of events, there were no significant differences or tendencies in survival. For IHC, MED15 was found to have a higher expression in non-muscle invasive BCa compared with benign and muscle invasive BCa. For survival analysis, no significant differences between samples with or without overexpression of MED15 were found. In the functional analysis, proliferation, migration, and invasion were significantly reduced in BCa-cells following the transient siRNA-mediated MED15 knockdown. In summary, MED15 appears to play a role in the tumor parameters proliferation, migration, and invasion in BCa, but further investigations are necessary. D.A. Spandidos 2018-09 2018-06-25 /pmc/articles/PMC6096071/ /pubmed/30127891 http://dx.doi.org/10.3892/ol.2018.9014 Text en Copyright: © Syring et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Syring, Isabella
Weiten, Richard
Müller, Tim
Schmidt, Doris
Steiner, Susanne
Kristiansen, Glen
Müller, Stefan C.
Ellinger, Jörg
The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy
title The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy
title_full The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy
title_fullStr The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy
title_full_unstemmed The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy
title_short The knockdown of the Mediator complex subunit MED15 restrains urothelial bladder cancer cells' malignancy
title_sort knockdown of the mediator complex subunit med15 restrains urothelial bladder cancer cells' malignancy
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6096071/
https://www.ncbi.nlm.nih.gov/pubmed/30127891
http://dx.doi.org/10.3892/ol.2018.9014
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