The use of panel testing in familial breast and ovarian cancer.
Published version
Peer-reviewed
Repository URI
Repository DOI
Change log
Authors
Abstract
Advances in sequencing technology have led to the introduction of panel testing in hereditary breast and ovarian cancer. While direct-to-consumer testing services have become widely available, the clinical validity of many of the genes on panel tests remains contentious and risk management guidelines are often lacking. This article gives an overview of advantages with panel testing as well as important challenges, including clinical translation of test results.
Description
Keywords
breast cancer, gene panel, genetic testing and hereditary cancer, ovarian cancer, AMP-Activated Protein Kinase Kinases, Antigens, CD, Cadherins, DNA-Binding Proteins, Epithelial Cell Adhesion Molecule, Female, Genes, BRCA1, Genes, BRCA2, Genetic Predisposition to Disease, Genetic Testing, Hereditary Breast and Ovarian Cancer Syndrome, High-Throughput Nucleotide Sequencing, Humans, Li-Fraumeni Syndrome, Lynch Syndrome II, MutL Protein Homolog 1, MutS Homolog 2 Protein, PTEN Phosphohydrolase, Peutz-Jeghers Syndrome, Protein Serine-Threonine Kinases, Sequence Analysis, DNA, Tumor Suppressor Protein p53
Journal Title
Clin Med (Lond)
Conference Name
Journal ISSN
1470-2118
1473-4893
1473-4893
Volume Title
17
Publisher
Elsevier BV
Publisher DOI
Sponsorship
European Research Council (310018)