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The value of cell-free DNA for molecular pathology

期刊

JOURNAL OF PATHOLOGY
卷 244, 期 5, 页码 616-627

出版社

WILEY
DOI: 10.1002/path.5048

关键词

liquid biopsy; cell-free nucleic acids; circulating tumour DNA; genomics; PCR; DNA sequencing; molecular pathology; cancer

资金

  1. Department of Pathology of the Memorial Sloan Kettering Cancer Center
  2. Department of Pediatrics of the Memorial Sloan Kettering Cancer Center
  3. Marie-Jose and Henry R. Kravis Center for Molecular Oncology of the Memorial Sloan Kettering Cancer Center
  4. Memorial Sloan Kettering Cancer Center Support Grant (NIH/NCI) [P30CA008748]
  5. University of Cambridge
  6. Cancer Research UK
  7. National Breast Cancer Foundation
  8. Victorian Cancer Agency, Australia
  9. National Breast Cancer Foundation [ECF-14-027] Funding Source: researchfish

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Over the past decade, advances in molecular biology and genomics techniques have revolutionized the diagnosis and treatment of cancer. The technological advances in tissue profiling have also been applied to the study of cell-free nucleic acids, an area of increasing interest for molecular pathology. Cell-free nucleic acids are released from tumour cells into the surrounding body fluids and can be assayed non-invasively. The repertoire of genomic alterations in circulating tumour DNA (ctDNA) is reflective of both primary tumours and distant metastatic sites, and ctDNA can be sampled multiple times, thereby overcoming the limitations of the analysis of single biopsies. Furthermore, ctDNA can be sampled regularly to monitor response to treatment, to define the evolution of the tumour genome, and to assess the acquisition of resistance and minimal residual disease. Recently, clinical ctDNA assays have been approved for guidance of therapy, which is an exciting first step in translating cell-free nucleic acid research tests into clinical use for oncology. In this review, we discuss the advantages of cell-free nucleic acids as analytes in different body fluids, including blood plasma, urine, and cerebrospinal fluid, and their clinical applications in solid tumours and haematological malignancies. We will also discuss practical considerations for clinical deployment, such as preanalytical factors and regulatory requirements. Copyright (c) 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.

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