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PMID: 2830575 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Reduced protein kinase C activity in a ras-resistant cell line derived from Ki-MSV transformed cells.

Oncogene ·Vol. 1 ·No. 1 ·1987-03-00 ·Pages 37-46

Kamata T, Sullivan NF, Wooten MW

Abstract

We have examined phosphatidylinositol turnover and C-kinase distribution in a flat cellular ras-resistant cell line (C11) derived from Kirsten murine sarcoma virus (Ki-MSV) transformed NIH/3T3 cells (DT). This cell type has been shown to express high levels of the p21 Ki-ras gene product yet is resistant to the transforming effects of this protein. Our data indicate that C11 cells have reduced levels of total C-kinase activity when compared to NIH/3T3 cells and do not retain the ability to phosphorylate the growth associated 80-kDa C-kinase substrate either in vivo or in vitro. Furthermore, whilst the steady state levels of diacylglycerol and the sum of inositol phosphates are elevated in DT cells, in C11 cells these levels are reduced to an amount equivalent to that seen in NIH/3T3 cells. These data indicate a correlation between a protein kinase C dependent pathway and resistance to transformation by ras.

MeSH Terms
Cell Compartmentation Cell Line Cell Membrane/enzymology Cell Transformation, Viral Cytoplasm/enzymology Diglycerides/metabolism Gene Expression Regulation/drug effects Genes, ras Kirsten murine sarcoma virus/genetics Molecular Weight Phosphatidylinositols/metabolism Phosphoproteins/metabolism Protein Kinase C/metabolism Tetradecanoylphorbol Acetate/pharmacology
Chemicals
Diglycerides Phosphatidylinositols Phosphoproteins Protein Kinase C Tetradecanoylphorbol Acetate
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Kamata T
Cold Spring Harbor Laboratory, New York 11724.
Sullivan N F
Wooten M W
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1987-03-00
Pages
37-46
Language
English
Region
England
NLM ID
8711562
Subset
IM
Grants
NCI NIH HHS · CA13106 · United States
NCI NIH HHS · CA39811 · United States
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