Abstract
Mapping tumour cell protein networks in routinely processed clinical samples, such as formalin-fixed and paraffin-embedded (FFPE) breast cancer tissues, will be critical for realizing the promise of personalized molecular therapy as only a subset of patients will respond. The quantification and characterisation of deregulated signalling molecules, including HER2, is a very promising approach for the identification of new suitable therapy targets and for the selection of those patients who will receive the greatest benefit from individualised treatments. In this regard the reverse phase protein array (RPPA) is a powerful technology for quick and simultaneous analysis of many patient samples allowing relative and absolute protein quantifications. Importantly, it requires only limited amounts of routine clinical material (e.g. biopsies). In this article we present a straight forward approach for extract-based determination of protein levels for HER2 and downstream signalling molecules in FFPE cancer tissues in order to define patient subgroups for therapy.
| Original language | English |
|---|---|
| Title of host publication | HER2 and Cancer |
| Subtitle of host publication | Mechanism, Testing and Targeted Therapy |
| Publisher | Nova Science Publishers, Inc. |
| Pages | 211-216 |
| Number of pages | 6 |
| ISBN (Print) | 9781611226508 |
| State | Published - Feb 2011 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Deregulated signalling pathways
- Formalin-fixed and paraffin embedded tissues (FFPE)
- Human epidermal growth factor receptor 2 (HER2)
- Reverse phase protein array (RPPA)
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