| Literature DB >> 15159020 |
Jürgen Sonnemann1, Volker Gekeler, Katrin Ahlbrecht, Klaus Brischwein, Chao Liu, Peter Bader, Cornelia Müller, Dietrich Niethammer, James F Beck.
Abstract
Previous studies point to protein kinase C (PKC) isozyme eta as a resistance factor in cancer cells. Therefore, we investigated whether down-regulation of PKCeta with second generation antisense oligonucleotides (ODNs) would sensitise A549 human lung carcinoma cells to cytostatics. The effects were compared to the outcome of Bcl-xL down-regulation. Upon treatment with antisense ODNs, PKCeta and Bcl-xL were both significantly reduced on mRNA and protein level. Down-regulation of either PKCeta or Bcl-xL in combination with vincristine or paclitaxel resulted in a significant increase in caspase-3 activity compared to that in the control oligonucleotide treated cells. In addition, PKCeta down-regulation augmented vincristine-induced dissipation of mitochondrial transmembrane potential. In conclusion, these results confirm that PKCeta might represent a considerable resistance factor and an interesting target to improve anticancer chemotherapy. Copyright 2004 Elsevier Ltd.Entities:
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Year: 2004 PMID: 15159020 DOI: 10.1016/j.canlet.2004.02.001
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679