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The translation of discoveries on extracellular vesicle (EV) based cancer biomarkers to personalised precision oncology requires the development of robust, sensitive and specific assays that are amenable to adoption in the clinical laboratory. Whilst a variety of elegant approaches for EV liquid biopsy have been developed, most of them remain as research prototypes due to the requirement of a high level of microfabrication and/or sophisticated instruments. Hence, this study is set to develop a simple DNA aptamer-enabled and fluorescence polarisation-based homogenous assay that eliminates the need to separate unbound detection ligands from the bound species for EV detection.

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Article Synopsis
  • The tendency for solid cancers to spread (metastasize) is crucial for determining patient prognosis, and recent findings show that micrometastases can develop much earlier than previously recognized.
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  • The current cancer staging methods may need updates to accurately reflect cancer presence in different areas of the body, and early therapies for small-scale cancer spread could help prevent more severe disease later on, especially in high-risk cases like skin cancer.
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Recent progress in our understanding of cancer mostly relies on the systematic profiling of patient samples with high-throughput techniques like transcriptomics. With this approach, one can find gene signatures and networks underlying cancer aggressiveness and therapy resistance. However, omics data alone cannot generate insights into the spatiotemporal aspects of tumor progression.

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