Journal article

Using the MCF10A/MCF10CA1a breast cancer progression cell line model to investigate the effect of active, mutant forms of EGFR in breast cancer development and treatment using gefitinib

DC Bessette, E Tilch, T Seidens, MCJ Quinn, AP Wiegmans, W Shi, S Cocciardi, A McCart-Reed, JM Saunus, PT Simpson, SM Grimmond, SR Lakhani, KK Khanna, N Waddell, F Al-Ejeh, G Chenevix-Trench

Plos One | Published : 2015

Abstract

Background: Basal-like and triple negative breast cancer (TNBC) share common molecular features, poor prognosis and a propensity for metastasis to the brain. Amplification of epidermal growth factor receptor (EGFR) occurs in ∼50% of basal-like breast cancer, and mutations in the epidermal growth factor receptor (EGFR) have been reported in up to ∼ 10% of Asian TNBC patients. In non-small cell lung cancer several different mutations in the EGFR tyrosine kinase domain confer sensitivity to receptor tyrosine kinase inhibitors, but the tumourigenic potential of EGFR mutations in breast cells and their potential for targeted therapy is unknown. Materials and Methods: Constructs containing wild ty..

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University of Melbourne Researchers

Grants

Awarded by National Health and Medical Research Council


Funding Acknowledgements

This work was funded by the National Health and Medical Research Council Australia (Programme Grant No. 1017028). In addition, APW and PTS are funded by fellowships from the National Breast Cancer Foundation, Australia; GCT is a Senior Principal Research Fellow of the NHMRC. ET was supported by the Max Weber-Programm des Freistaates Bayern zur Hochbegabtenforderung nach dem Bayerischen Eliteforderungsgesetz of the State of Bavaria and a grant from the Deans' Office of the faculty for chemistry and pharmacy of the Ludwig-Maximilians University.