Atypical protein kinase C-zeta modulates clonogenicity, motility, and secretion of proteolytic enzymes in murine mammary cells.

Abstract

In this paper, we investigated whether protein kinase C-zeta (PKC zeta), a member of the atypical PKC family, induces phenotypic alterations associated with malignant transformation and tumor progression in mammary cells. The stable overexpression of PKC zeta in immortalized mammary epithelial cells (NMuMG), activates the mitogenic extracellular signal-regulated kinase (ERK) pathway, enhanced clonal cell growth and exerts profound effects on proteases secretion. The effect on proteases expression seems to be specific for urokinase-type plasminogen activator and metalloproteinase-9 (MMP-9) because no modulation in MMP-2 and MMP-3 production could be detected. In addition, our experiments demonstrated that PKC zeta overexpression markedly altered the adhesive, spreading, and migratory abilities of NMuMG cells. The overexpression of this enzyme was not sufficient to confer an anchorage-independent growth capacity. An extensive mutational analysis of PKC zeta revealed that the effects observed in NMuMG cells were strictly dependent on the kinase (catalytic) domain of the enzyme. Taken together, these results suggest that in mammary cells PKC zeta modulates several of the critical events involved in tumor development and dissemination through the activation of mitogen activated protein kinase (MAPK)/ERK pathway.

• Authors: Alejandro J Urtreger, Valeria C Grossoni, Karina B Falbo, Marcelo G Kazanietz, Elisa D Bal de Kier Joffé
• Journal: Molecular carcinogenesis (Mol Carcinog) Vol. 42 Issue 1 Pg. 29-39 (Jan 2005) ISSN: 0899-1987 [Print] United States
• PMID: 15546134 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• PKC-3 protein
• Protein Kinase C
• Mitogen-Activated Protein Kinase 1
• Mitogen-Activated Protein Kinase 3
• Peptide Hydrolases
• Matrix Metalloproteinases

Topics

• Animals
• Cell Division (physiology)
• Cell Movement (physiology)
• Cell Survival (physiology)
• Female
• Mammary Glands, Animal (cytology, metabolism)
• Matrix Metalloproteinases (metabolism)
• Mice
• Mitogen-Activated Protein Kinase 1 (metabolism)
• Mitogen-Activated Protein Kinase 3 (metabolism)
• Peptide Hydrolases (metabolism)
• Protein Kinase C (metabolism)