Back to Search
Start Over
Protein kinase C Inhibitors selectively modulate dynamics of cell adhesion molecules and cell death in human colon cancer cells.
- Source :
-
Cell adhesion & migration [Cell Adh Migr] 2019 Dec; Vol. 13 (1), pp. 83-97. Date of Electronic Publication: 2018 Oct 11. - Publication Year :
- 2019
-
Abstract
- 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.
- Subjects :
- Autophagy
Collagen metabolism
Colonic Neoplasms drug therapy
Colonic Neoplasms metabolism
Humans
Reactive Oxygen Species metabolism
Tumor Cells, Cultured
Apoptosis drug effects
Cell Adhesion
Cell Adhesion Molecules metabolism
Colonic Neoplasms pathology
Gene Expression Regulation, Neoplastic drug effects
Protein Kinase C antagonists & inhibitors
Protein Kinase Inhibitors pharmacology
Subjects
Details
- Language :
- English
- ISSN :
- 1933-6926
- Volume :
- 13
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Cell adhesion & migration
- Publication Type :
- Academic Journal
- Accession number :
- 30289336
- Full Text :
- https://doi.org/10.1080/19336918.2018.1530933