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Identification of Novel CK2 Kinase Substrates Using a Versatile Biochemical Approach
Published on: February 21, 2019
Multifunctional roles of PKCδ: Opportunities for targeted therapy in human disease
Mary E Reyland1, David N M Jones2
1Department of Craniofacial Biology, School of Dental Medicine, University of Colorado Anschutz Medical Campus, Aurora, CO 80045, USA.
Abstract:
The serine-threonine protein kinase, protein kinase C-δ (PKCδ), is emerging as a bi-functional regulator of cell death and proliferation. Studies in PKCδ-/- mice have confirmed a pro-apoptotic role for this kinase in response to DNA damage and a tumor promoter role in some oncogenic contexts. In non-transformed cells, inhibition of PKCδ suppresses the release of cytochrome c and caspase activation, indicating a function upstream of apoptotic pathways. Data from PKCδ-/- mice demonstrate a role for PKCδ in the execution of DNA damage-induced and physiologic apoptosis. This has led to the important finding that inhibitors of PKCδ can be used therapeutically to reduce irradiation and chemotherapy-induced toxicity. By contrast, PKCδ is a tumor promoter in mouse models of mammary gland and lung cancer, and increased PKCδ expression is a negative prognostic indicator in Her2+ and other subtypes of human breast cancer. Understanding how these distinct functions of PKCδ are regulated is critical for the design of therapeutics to target this pathway. This review will discuss what is currently known about biological roles of PKCδ and prospects for targeting PKCδ in human disease.
Insights
Protein kinase C-delta (PKCδ) has dual roles in cell death and proliferation. Inhibiting PKCδ may reduce chemotherapy toxicity, but it also promotes tumor growth in some cancers.
Area of Science:
- Cellular Biology
- Molecular Oncology
- Biochemistry
Background:
- Protein kinase C-delta (PKCδ) is a serine-threonine kinase with a newly recognized dual role in regulating cell death and proliferation.
- Studies in knockout mice reveal PKCδ's pro-apoptotic function in response to DNA damage and its role as a tumor promoter in certain cancers.
- PKCδ acts upstream of apoptotic pathways, as inhibiting it suppresses cytochrome c release and caspase activation in non-transformed cells.
Purpose of the Study:
- To review the current understanding of PKCδ's biological functions.
- To explore the prospects of targeting PKCδ for therapeutic interventions in human diseases.
- To elucidate the regulatory mechanisms underlying PKCδ's distinct roles in cell death and proliferation.
Main Methods:
- Review of existing literature and studies involving PKCδ knockout mice.
- Analysis of data on PKCδ expression in human breast cancer subtypes.
- Examination of cellular assays investigating apoptotic pathway regulation.
Main Results:
- PKCδ deficiency protects against DNA damage-induced and physiological apoptosis.
- PKCδ inhibition reduces irradiation and chemotherapy-induced toxicity.
- PKCδ acts as a tumor promoter in mouse models of mammary gland and lung cancer.
- Elevated PKCδ expression correlates with poor prognosis in Her2+ and other breast cancer subtypes.
Conclusions:
- PKCδ exhibits opposing roles, acting as a pro-apoptotic factor and a tumor promoter.
- Targeting PKCδ presents a therapeutic opportunity for managing treatment toxicity.
- Further research into PKCδ regulation is crucial for developing effective cancer therapies.
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