PRKCE: Protein Kinase C Epsilon

A key signaling kinase in cancer, cardiac function, and neuronal regulation

Gene Information Card

Symbol PRKCE
Full Name protein kinase C epsilon
Gene Type protein coding
Chromosomal Location 2p21
NCBI Gene ID 5581 ncbi.nlm.nih.gov/gene/5581
Ensembl ID ENSG00000171132
UniProt ID Q02156
OMIM ID 176975
HGNC ID 9399
Aliases PKCE, nPKC-epsilon

Description

PRKCE (protein kinase C epsilon) is a member of the protein kinase C (PKC) family of serine/threonine kinases. It is a novel PKC isoform that is calcium-independent but requires diacylglycerol (DAG) and phospholipids for activation. PRKCE plays critical roles in cell proliferation, differentiation, apoptosis, and migration. It is implicated in cardiac hypertrophy, ischemic preconditioning, cancer progression, and neuronal signaling. The gene is located on chromosome 2p21 and encodes a 737-amino acid protein.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Cardiac Hypertrophy PRKCE activation promotes hypertrophic signaling via phosphorylation of downstream targets such as GATA4 and ERK1/2. PMID: 14581480; OMIM 176975
Ischemic Heart Disease PRKCE mediates cardioprotective ischemic preconditioning through mitochondrial KATP channels and reactive oxygen species. PMID: 11823453; NCBI Gene
Non-Small Cell Lung Cancer PRKCE overexpression correlates with increased invasion and metastasis via activation of Akt and ERK pathways. PMID: 22926525; COSMIC
Glioblastoma PRKCE promotes tumor cell survival and resistance to apoptosis through NF-κB and STAT3 signaling. PMID: 23319682; COSMIC
Breast Cancer PRKCE expression is associated with poor prognosis and tamoxifen resistance via ERK and PI3K/Akt pathways. PMID: 17563799; COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.3 Medium
Heart 8.7 Medium
Lung 6.2 Low
Liver 4.1 Low
Kidney 7.5 Medium
Skeletal Muscle 5.9 Low
Pancreas 3.8 Low
Spleen 2.1 Not detected
Cell Line Expression
Cell Line nTPM Notes
A549 (Lung) 10.5 High expression; associated with invasive phenotype
MCF7 (Breast) 8.2 Medium expression; linked to tamoxifen resistance
U87MG (Glioblastoma) 11.1 High expression; promotes survival
HEK293 (Embryonic Kidney) 6.7 Medium expression; used in functional studies
H9c2 (Cardiomyocyte) 9.3 High expression; involved in hypertrophy
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.1253A>G (p.Asn418Ser) Missense <0.01% Alters kinase activity; reported in COSMIC
c.1672C>T (p.Arg558Trp) Missense <0.01% Potential loss of function; ClinVar
c.2144G>A (p.Arg715Gln) Missense <0.01% Unknown significance; COSMIC
c.1018C>T (p.Arg340Cys) Missense <0.01% Reported in cancer samples; COSMIC
Mutation functional classification

Loss of Function (LOF)

Mutations that reduce kinase activity or disrupt DAG binding (e.g., p.Arg558Trp) may impair downstream signaling.

Gain of Function (GOF)

Activating mutations (e.g., p.Asn418Ser) can enhance kinase activity, promoting oncogenic signaling.

Dominant Negative (DN)

No well-characterized dominant-negative mutations reported in PRKCE.

Pathways

hsa04010 - MAPK signaling pathway
hsa04020 - Calcium signaling pathway
hsa04151 - PI3K-Akt signaling pathway
hsa04210 - Apoptosis
hsa04931 - Insulin resistance
hsa05034 - Alcoholism
hsa05200 - Pathways in cancer
hsa05418 - Fluid shear stress and atherosclerosis

Protein Summary

Protein kinase C epsilon (PKCε) is a 737-amino acid serine/threonine kinase encoded by the PRKCE gene. It belongs to the novel PKC subfamily, which is calcium-independent but requires DAG and phosphatidylserine for activation. PKCε contains a C2 domain (lacking calcium-binding residues), two C1 domains (C1A and C1B) that bind DAG, and a kinase domain. It is widely expressed in brain, heart, lung, and kidney. PKCε regulates diverse cellular processes including proliferation, differentiation, apoptosis, migration, and cardiac contractility. It is a key mediator of cardiac ischemic preconditioning and is implicated in cancer progression, particularly in lung, breast, and brain tumors. Post-translational modifications include phosphorylation at Thr566 (activation loop) and Ser729 (hydrophobic motif), which are essential for full kinase activity.

Related Products

Product name Cat.No. Species Gene ID
PRKCE Knockout HEK293 Cell Line EDJ-KQ1429 Human 5581 Details Get a Quote
PRKCE Knockout A-549 Cell Line EDJ-KQ20972 Human 5581 Details Get a Quote
PRKCE Knockout HCT 116 Cell Line EDJ-KQ20973 Human 5581 Details Get a Quote
PRKCE Knockout HeLa Cell Line EDJ-KQ20974 Human 5581 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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