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Induction and Analysis of Epithelial to Mesenchymal Transition
Published on: August 27, 2013
Evidence that v-src and v-fps gene products use a protein kinase C-mediated pathway to induce expression of a
R Spangler1, C Joseph, S A Qureshi
1Institute for Biomolecular Structure and Function, Hunter College, City University of New York, NY 10021.
Abstract:
Induction of the transformation-related gene 9E3 by the v-src and v-fps gene products (v-Src and v-Fps) is blocked in chicken embryo fibroblasts depleted of protein kinase C (PKC). PKC agonists induce 9E3 gene expression. Protein kinase inhibitors block v-Src- and v-Fps-induced 9E3 gene expression with the same dose-response curves seen for PKC agonist-induced 9E3 gene expression. These data suggest that v-Src and v-Fps use a PKC-mediated signal-transduction pathway to induce expression of the transformation-related 9E3 gene. Consistent with this hypothesis, we find that both v-Src and v-Fps rapidly induce phosphorylation of a 67-kDa PKC substrate.
Insights
The study reveals that protein kinase C (PKC) is crucial for the v-Src and v-Fps oncogenes to induce the transformation-related gene 9E3. This suggests a PKC-mediated signaling pathway is involved in cancer-related gene expression.
Area of Science:
- Molecular Biology
- Cell Signaling
- Oncogenesis
Background:
- The v-src and v-fps oncogenes are known to induce cellular transformation.
- The transformation-related gene 9E3 is implicated in cellular processes.
- Protein kinase C (PKC) is a family of enzymes involved in various cellular signaling pathways.
Purpose of the Study:
- To investigate the role of protein kinase C (PKC) in the induction of the 9E3 gene by v-Src and v-Fps oncogenes.
- To elucidate the signal-transduction pathway utilized by v-Src and v-Fps for 9E3 gene expression.
Main Methods:
- Depletion of protein kinase C (PKC) in chicken embryo fibroblasts.
- Treatment with PKC agonists and protein kinase inhibitors.
- Analysis of 9E3 gene expression.
- Assay for phosphorylation of a 67-kDa PKC substrate.
Main Results:
- Depletion of PKC blocked v-Src- and v-Fps-induced 9E3 gene expression.
- PKC agonists induced 9E3 gene expression.
- Protein kinase inhibitors mimicked the dose-response of PKC agonists in blocking v-Src- and v-Fps-induced 9E3 expression.
- Both v-Src and v-Fps rapidly induced phosphorylation of a 67-kDa PKC substrate.
Conclusions:
- v-Src and v-Fps oncogenes utilize a protein kinase C (PKC)-mediated signal-transduction pathway to induce the transformation-related 9E3 gene.
- PKC activation is a key event in the signaling cascade initiated by v-Src and v-Fps leading to 9E3 gene expression.
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