Exploring mechanisms of acquired resistance to HER2 (human epidermal growth factor receptor 2)-targeted therapies in breast cancer

Helen Creedon, Adam Byron, Joanna Main, Larry Hayward, Teresa Klinowska, Valerie G Brunton

Research output: Contribution to journalArticle

Abstract / Description of output

HER2 (human epidermal growth factor receptor 2)-targeted therapy in breast cancer is one of the earliest and arguably most successful examples of the modern class of targeted drugs. Initially identified in the 1980s, the observation that HER2 acts as an independent predictor of poor prognosis in the 20% of breast cancer cases carrying a gene amplification or protein overexpression cemented its place at the forefront of research in this field. The outlook for patients with HER2-positive breast cancer has been revolutionized by the introduction of HER2-targeted agents, such as trastuzumab and lapatinib, yet resistance is frequently encountered and multiple different resistance mechanisms have been identified. We have explored resistance to a novel pan-HER inhibitor, AZD8931, and we examine mechanisms of resistance common to trastuzumab, lapatinib and AZD8931, and discuss the current problems associated with translating the wealth of pre-clinical data into clinical benefit.

Original languageEnglish
Pages (from-to)822-30
JournalBiochemical Society Transactions
Volume42
Issue number4
Early online date1 Aug 2014
DOIs
Publication statusPublished - Aug 2014

Keywords / Materials (for Non-textual outputs)

  • Antibodies, Monoclonal, Humanized
  • Antineoplastic Agents
  • Breast Neoplasms
  • Drug Resistance, Neoplasm
  • Female
  • Humans
  • Quinazolines
  • Receptor, ErbB-2

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