Cargando…

Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells

During development of colon cancer, Protein Kinase Cs (PKCs) are involved in regulation of many genes controlling several cellular mechanisms. Here, we examined the changes in cell adhesion molecules and PKCs for colorectal cancer progression. We identified that PKCs affected expression of EpCAM, cl...

Descripción completa

Detalles Bibliográficos
Autores principales: Dükel, Muzaffer, Tavsan, Zehra, Erdogan, Duygu, Erkan Gök, Deniz, Ayar Kayali, Hulya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527378/
https://www.ncbi.nlm.nih.gov/pubmed/30289336
http://dx.doi.org/10.1080/19336918.2018.1530933
_version_ 1783420025240027136
author Dükel, Muzaffer
Tavsan, Zehra
Erdogan, Duygu
Erkan Gök, Deniz
Ayar Kayali, Hulya
author_facet Dükel, Muzaffer
Tavsan, Zehra
Erdogan, Duygu
Erkan Gök, Deniz
Ayar Kayali, Hulya
author_sort Dükel, Muzaffer
collection PubMed
description During development of colon cancer, Protein Kinase Cs (PKCs) are involved in regulation of many genes controlling several cellular mechanisms. Here, we examined the changes in cell adhesion molecules and PKCs for colorectal cancer progression. We identified that PKCs affected expression of EpCAM, claudins, tetraspanins. Treatment with low concentrations of PKC inhibitors resulted in decreased cell viability. In addition, immunoblotting and qRT-PCR analysis showed that apoptosis was inhibited while autophagy was induced by PKC inhibition in colon cancer cells. Furthermore, we observed decreased levels of intracellular Reactive Oxygen Species (ROS), lipid peroxidation and protein carbonyl, confirming the ROS-induced apoptosis. Taken together, our results reveal that PKC signalling modulates not only cell adhesion dynamics but also cell death-related mechanisms. Abbreviations: PKC: Protein Kinase C; EpCAM: Epithelial cell adhesion molecule; FBS: fetal bovine serum; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide); CAM: cell adhesion molecule; ROS: reactive oxygen species
format Online
Article
Text
id pubmed-6527378
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-65273782019-05-31 Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells Dükel, Muzaffer Tavsan, Zehra Erdogan, Duygu Erkan Gök, Deniz Ayar Kayali, Hulya Cell Adh Migr Research Article During development of colon cancer, Protein Kinase Cs (PKCs) are involved in regulation of many genes controlling several cellular mechanisms. Here, we examined the changes in cell adhesion molecules and PKCs for colorectal cancer progression. We identified that PKCs affected expression of EpCAM, claudins, tetraspanins. Treatment with low concentrations of PKC inhibitors resulted in decreased cell viability. In addition, immunoblotting and qRT-PCR analysis showed that apoptosis was inhibited while autophagy was induced by PKC inhibition in colon cancer cells. Furthermore, we observed decreased levels of intracellular Reactive Oxygen Species (ROS), lipid peroxidation and protein carbonyl, confirming the ROS-induced apoptosis. Taken together, our results reveal that PKC signalling modulates not only cell adhesion dynamics but also cell death-related mechanisms. Abbreviations: PKC: Protein Kinase C; EpCAM: Epithelial cell adhesion molecule; FBS: fetal bovine serum; MTT: 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide); CAM: cell adhesion molecule; ROS: reactive oxygen species Taylor & Francis 2018-10-11 /pmc/articles/PMC6527378/ /pubmed/30289336 http://dx.doi.org/10.1080/19336918.2018.1530933 Text en © 2019 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Dükel, Muzaffer
Tavsan, Zehra
Erdogan, Duygu
Erkan Gök, Deniz
Ayar Kayali, Hulya
Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
title Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
title_full Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
title_fullStr Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
title_full_unstemmed Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
title_short Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
title_sort protein kinase c inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527378/
https://www.ncbi.nlm.nih.gov/pubmed/30289336
http://dx.doi.org/10.1080/19336918.2018.1530933
work_keys_str_mv AT dukelmuzaffer proteinkinasecinhibitorsselectivelymodulatedynamicsofcelladhesionmoleculesandcelldeathinhumancoloncancercells
AT tavsanzehra proteinkinasecinhibitorsselectivelymodulatedynamicsofcelladhesionmoleculesandcelldeathinhumancoloncancercells
AT erdoganduygu proteinkinasecinhibitorsselectivelymodulatedynamicsofcelladhesionmoleculesandcelldeathinhumancoloncancercells
AT erkangokdeniz proteinkinasecinhibitorsselectivelymodulatedynamicsofcelladhesionmoleculesandcelldeathinhumancoloncancercells
AT ayarkayalihulya proteinkinasecinhibitorsselectivelymodulatedynamicsofcelladhesionmoleculesandcelldeathinhumancoloncancercells