Abstract
Recent developments in massively parallel sequencing and digital genomic techniques support the clinical validity of cell-free circulating tumour DNA (ctDNA) as a 'liquid biopsy' in human cancer. In breast cancer, ctDNA detected in plasma can be used to non-invasively scan tumour genomes and quantify tumour burden. The applications for ctDNA in plasma include identifying actionable genomic alterations, monitoring treatment responses, unravelling therapeutic resistance, and potentially detecting disease progression before clinical and radiological confirmation. ctDNA may be used to characterise tumour heterogeneity and metastasis-specific mutations providing information to adapt the therapeutic management of patients. In this article, we review the current status of ctDNA as a 'liquid biopsy' in breast cancer.
| Original language | English |
|---|---|
| Pages (from-to) | 464-474 |
| Number of pages | 11 |
| Journal | Molecular Oncology |
| Volume | 10 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1 Mar 2016 |
| Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2015 Federation of European Biochemical Societies.
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
- Breast cancer
- Circulating cell-free tumour DNA
- Heterogeneity
- Monitoring
- Resistance
- Stratification
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