Erschienen in:
01.06.2010 | PRECLINICAL STUDIES
Screening of a PKC ζ-specific kinase inhibitor PKCzI257.3 which inhibits EGF-induced breast cancer cell chemotaxis
verfasst von:
Jing Wu, Baogang Zhang, Min Wu, Hongyan Li, Ruifang Niu, Guoguang Ying, Ning Zhang
Erschienen in:
Investigational New Drugs
|
Ausgabe 3/2010
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Summary
Chemotaxis has recently been implicated in tumor metastasis. Protein Kinase C(PKC)ζ is often over-activated and is a key signal transducer shared by both EGFR- and CXCR4-mediated chemotactic signaling in human breast and lung cancers, as well as CSF-1-induced macrophage migration. In order to develop potential inhibitors targeting PKCζ for effective blockage of cancer cell chemotaxis and tumor metastasis, the Z′-LYTE™ KINASE ASSAY -SER/THR 7 PEPTIDE Kit was used and a compound called PKCzI257.3 was identified with IC50 of 28 µM. As a result of treatment, chemotactic migration potency of the human breast cancer cell MDA-MB-231 were impaired, while no significant effect was observed on cell proliferation. Furthermore, EGF-induced cofilin phosphorylation, a critical step of cofilin recycle and actin polymerization, was also dampened, which was relevant to the decreased cell migration. Our results suggest that PKCzI257.3 is a PKCζ-specific compound inhibitor which blocked cancer cell migration and may serve as a potential therapeutic drug for cancer treatment.