Protein kinase C beta II suppresses colorectal cancer by regulating IGF-1 mediated cell survival.
Ontology highlight
ABSTRACT: Despite extensive efforts, cancer therapies directed at the Protein Kinase C (PKC) family of serine/threonine kinases have failed in clinical trials. These therapies have been directed at inhibiting PKC and have, in some cases, worsened disease outcome. Here we examine colon cancer patients and show not only that PKC Beta II is a tumour suppressor, but patients with low levels of this isozyme have significantly decreased disease free survival. Specifically, analysis of gene expression levels of all PKC genes in matched normal and cancer tissue samples from colon cancer patients revealed a striking down-regulation of the gene coding PKC Beta in the cancer tissue (n = 21). Tissue microarray analysis revealed a dramatic down-regulation of PKC Beta II protein levels in both the epithelial and
SUBMITTER: Dowling CM
PROVIDER: S-EPMC4991501 | biostudies-literature | 2016 Apr
REPOSITORIES: biostudies-literature
ACCESS DATA