Poster Presentation 29th Lorne Cancer Conference 2017

The role of periostin in tumour cell migration, apoptosis, invasion and proliferation in vitro (#268)

Lynda A Sharp 1 , Dodie Pouniotis 1 , Ian Darby 1
  1. Health and Biomedical Science, RMIT, Bundoora, VIC, Australia

Abstract

The role of periostin in tumour cell migration, apoptosis, invasion and proliferation in vitro

Lynda Sharp1,2, Dr. Dodie S. Pouniotis1,2, Ian A. Darby1,2

1Cancer & Tissue Repair Laboratory, RMIT University, Bundoora, VIC 3083, Australia

2School of Health & Biomedical Sciences, RMIT University, Bundoora, VIC 3083, Australia

 

 

Introduction

 

Periostin (PSTN) is a secreted 90kDa protein, preferentially expressed in embryogenesis and differentially expressed in certain types of normal adult connective tissue.  Overexpression of periostin in various human tumours and/or its associated tumour stroma has been shown to correlate with advanced disease and high mortality.  We hypothesised that PSTN may play a significant role in tumour growth and spread via a variety of tumour effector functions. Using murine (LLC) and human (A549) lung carcinoma cell lines, we show that PSTN expression has an influence on migration, proliferation, apoptosis and invasion in vitro.

Method

LLC & A549 cells were treated with: recombinant PSTN, transfected with PSTN plasmid or silenced for PSTN expression using esiRNA. Scratch assays were performed to determine tumour cell migration and flow cytometry to examine proliferation and apoptosis. Matrigel invasion and migration assays were performed to determine the effect of PSTN expression on cell invasion.  

Results

LLC-PSTN showed increased cell migration and proliferation whilst significantly reducing apoptosis in vitro.  PSTN silenced LLC cells showed a significant increase in early apoptosis while LLC and A549 cells treated with recombinant PSTN how significantly decreased apoptosis and increased migration and proliferation in vitro.

Conclusion

The data suggests PSTN plays a role in tumour cell migration, apoptosis and invasion/migration in vitro. These results may suggest the mechanism of increased periostin expression and advanced disease and needs to be further investigated in vivo.