Research Papers:

A small molecule inhibitor of atypical protein kinase C signaling inhibits pancreatic cancer cell transformed growth and invasion

Amanda M. Butler, Michele L. Scotti Buzhardt, Eda Erdogan, Shuhua Li, Kristin S. Inman, Alan P. Fields and Nicole R. Murray _

PDF  |  HTML  |  Supplementary Files  |  How to cite

Oncotarget. 2015; 6:15297-15310. https://doi.org/10.18632/oncotarget.3812

Metrics: PDF 2221 views  |   HTML 2799 views  |   ?  


Amanda M. Butler1, Michele L. Scotti Buzhardt2, Eda Erdogan3, Shuhua Li1, Kristin S. Inman1, Alan P. Fields1 and Nicole R. Murray1

1 Department of Cancer Biology, Mayo Clinic, Jacksonville, FL, USA

2 Genoptix/Novartis Molecular Diagnostics, Carlsbad, CA, USA

3 Department of Biomedical Sciences and Pathobiology, Virginia Polytechnic Institute and State University, Blacksburg, VA, USA

Correspondence to:

Nicole R. Murray, email:

Keywords: atypical PKCs, aurothiomalate, pancreatic cancer, transformed growth, invasion

Received: July 30, 2014 Accepted: March 10, 2015 Published: April 14, 2015


Pancreatic cancer is highly resistant to current chemotherapies. Identification of the critical signaling pathways that mediate pancreatic cancer transformed growth is necessary for the development of more effective therapeutic treatments. Recently, we demonstrated that protein kinase C iota (PKCι) and zeta (PKCζ) promote pancreatic cancer transformed growth and invasion, by activating Rac1→ERK and STAT3 signaling pathways, respectively. However, a key question is whether PKCι and PKCζ play redundant (or non-redundant) roles in pancreatic cancer cell transformed growth. Here we describe the novel observations that 1) PKCι and PKCζ are non-redundant in the context of the transformed growth of pancreatic cancer cells; 2) a gold-containing small molecule known to disrupt the PKCι/Par6 interaction, aurothiomalate, also disrupts PKCζ/Par6 interaction; 3) aurothiomalate inhibits downstream signaling of both PKCι and PKCζ, and blocks transformed growth of pancreatic cancer cells in vitro; and 4) aurothiomalate inhibits pancreatic cancer tumor growth and metastasis in vivo. Taken together, these data provide convincing evidence that an inhibitor of atypical PKC signaling inhibits two key oncogenic signaling pathways, driven non-redundantly by PKCι and PKCζ, to significantly reduce tumor growth and metastasis. Our results demonstrate that inhibition of atypical PKC signaling is a promising therapeutic strategy to treat pancreatic cancer.

Creative Commons License All site content, except where otherwise noted, is licensed under a Creative Commons Attribution 4.0 License.
PII: 3812