Breast cancer incidence in Europe reaches 430 000 cases every year.
Tumours with increased levels of the human epidermal growth factor
receptor 2 (HER2) are aggressive and associated with high mortality.
HER2 is a potent oncoprotein that has become an established target for
adjuvant treatment of breast cancer.
Despite the efficacy of anti-HER2 monoclonal antibodies, tumours still progress due to innate or acquired resistance to the treatment. There is an immediate need to develop innovative new, targeted agents for HER2 positive disease as well as identify HER2-related biomarkers for prediction, diagnosis, and monitoring of disease.
Seeking to address this, the EU-funded
IMAGINT (HER Imaging and molecular interaction mapping in breast cancer) project brought together an interdisciplinary team of researchers across Europe. The scientific plan focused on the therapeutic potential of the antibody-like proteins - designed ankyrin repeat proteins (DARPins). These are small molecules based on human protein scaffolds that can bind specific targets with high affinity.
IMAGINT developed a series of tools for synthesising and manipulating DARPins to carry specific chemical modifications and generated DARPins against different HER receptors. They went on to study the subcellular HER2 distribution and proposed this as a novel method for screening patient tissues.
Researchers discovered differences between breast cancer and corresponding healthy tissue using imaging cycler microscopy. Moreover, they detected alterations in associating miRNAs/proteins in response to anti-HER2 therapy. They also identified a number of breast cancer prognostic biomarkers following bioinformatic analysis of gene expression.
One of the IMAGINT imaging assays for identification of HER heterodimers demonstrated clinical applicability and prognostic value. Using this assay, scientists validated a new mechanism of resistance to anti-EGFR therapy in patients with triple-negative breast cancer. Furthermore, they developed a new agent allowing non-invasive whole body imaging of HER2+ tumours to provide information on disease spread and stage.
The identified biomarkers would help personalise treatment decisions and assist in the development of new drugs. For instance, early identification of patients at high risk of metastatic recurrence can help clinicians change their treatment strategy. Collectively, the deliverables of the IMAGINT study enable stratification and monitoring of breast cancer for hopefully better patient outcomes.