Atypical protein kinase C zeta: potential player in cell survival and cell migration of ovarian cancer.

Abstract

Ovarian cancer is one of the most aggressive gynaecological cancers, thus understanding the different biological pathways involved in ovarian cancer progression is important in identifying potential therapeutic targets for the disease. The aim of this study was to investigate the potential roles of Protein Kinase C Zeta (PRKCZ) in ovarian cancer. The atypical protein kinase C isoform, PRKCZ, is involved in the control of various signalling processes including cell proliferation, cell survival, and cell motility, all of which are important for cancer development and progression. Herein, we observe a significant increase in cell survival upon PRKCZ over-expression in SKOV3 ovarian cancer cells; additionally, when the cells are treated with small interference RNA (siRNA) targeting PRKCZ, the motility of SKOV3 cells decreased. Furthermore, we demonstrate that over-expression of PRKCZ results in gene and/or protein expression alterations of insulin-like growth factor 1 receptor (IGF1R) and integrin beta 3 (ITGB3) in SKOV3 and OVCAR3 cells. Collectively, our study describes PRKCZ as a potential regulatory component of the IGF1R and ITGB3 pathways and suggests that it may play critical roles in ovarian tumourigenesis.

• Authors: Kelly K Y Seto, Irene L Andrulis
• Journal: PloS one (PLoS One) Vol. 10 Issue 4 Pg. e0123528 ( 2015) ISSN: 1932-6203 [Electronic] United States
• PMID: 25874946 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Integrin beta3
• RNA, Small Interfering
• TIMP1 protein, human
• Tissue Inhibitor of Metalloproteinase-1
• Receptor, IGF Type 1
• protein kinase C zeta
• Protein Kinase C

Topics

• Cell Line, Tumor
• Cell Movement
• Cell Survival
• Female
• Humans
• Integrin beta3 (genetics, metabolism)
• Ovarian Neoplasms (metabolism, pathology)
• Protein Kinase C (antagonists & inhibitors, genetics, metabolism)
• RNA Interference
• RNA, Small Interfering (metabolism)
• Real-Time Polymerase Chain Reaction
• Receptor, IGF Type 1 (genetics, metabolism)
• Signal Transduction
• Tissue Inhibitor of Metalloproteinase-1 (genetics, metabolism)