Multiplexed assays for detection of mutations in PIK3CA.
dc.contributor.author | Board, Ruth E | |
dc.contributor.author | Thelwell, Nicola J | |
dc.contributor.author | Ravetto, Paul F | |
dc.contributor.author | Little, Stephen | |
dc.contributor.author | Ranson, Malcolm R | |
dc.contributor.author | Dive, Caroline | |
dc.contributor.author | Hughes, Andrew | |
dc.contributor.author | Whitcombe, David | |
dc.date.accessioned | 2009-04-21T16:41:15Z | |
dc.date.available | 2009-04-21T16:41:15Z | |
dc.date.issued | 2008-04 | |
dc.identifier.citation | Multiplexed assays for detection of mutations in PIK3CA. 2008, 54 (4):757-60 Clin. Chem. | en |
dc.identifier.issn | 0009-9147 | |
dc.identifier.pmid | 18375489 | |
dc.identifier.doi | 10.1373/clinchem.2007.098376 | |
dc.identifier.uri | http://hdl.handle.net/10541/65741 | |
dc.description.abstract | BACKGROUND: Mutations in the PIK3CA gene (phosphoinositide-3-kinase, catalytic, alpha polypeptide) have recently been described in a number of cancers, and their detection is currently limited because of the low sensitivity of conventional sequencing techniques. METHODS: We combined Amplification Refractory Mutation System (ARMS; AstraZeneca) allele-specific PCR and Scorpions (DxS) to develop assays for tumor-borne PIK3CA mutations and used real-time PCR to develop high-throughput multiplexed assays for the most commonly reported PIK3CA mutants (H1047L, H1047R, E542K, E545K). RESULTS: These assays were more sensitive than sequencing and could detect 5 copies of mutant DNA in proportions as low as 0.1% of the total DNA. We assayed DNA extracted from human tumors and detected PIK3CA mutation frequencies of 10.2% in colorectal cancer, 38.7% in breast cancer, 1.9% in lung cancer, and 2.9% in melanoma. In contrast, sequencing detected only 53% of the mutations detected by our assay. CONCLUSIONS: Multiplexed assays, which can easily be applied to clinical samples, have been developed for the detection of PIK3CA mutations. | |
dc.language.iso | en | en |
dc.subject | Breast Cancer | en |
dc.subject | Lung Cancer | en |
dc.subject | Colorectal Cancer | en |
dc.subject | PIK3CA | en |
dc.subject | Tumour Markers | en |
dc.subject.mesh | 1-Phosphatidylinositol 3-Kinase | |
dc.subject.mesh | Breast Neoplasms | |
dc.subject.mesh | Colorectal Neoplasms | |
dc.subject.mesh | Female | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Lung Neoplasms | |
dc.subject.mesh | Melanoma | |
dc.subject.mesh | Mutation | |
dc.subject.mesh | Polymerase Chain Reaction | |
dc.subject.mesh | Sensitivity and Specificity | |
dc.subject.mesh | Tumor Markers, Biological | |
dc.title | Multiplexed assays for detection of mutations in PIK3CA. | en |
dc.type | Article | en |
dc.contributor.department | Discovery Medicine, AstraZeneca Pharmaceuticals, Macclesfield, UK. ruth.board@astrazeneca.com | en |
dc.identifier.journal | Clinical Chemistry | en |
html.description.abstract | BACKGROUND: Mutations in the PIK3CA gene (phosphoinositide-3-kinase, catalytic, alpha polypeptide) have recently been described in a number of cancers, and their detection is currently limited because of the low sensitivity of conventional sequencing techniques. METHODS: We combined Amplification Refractory Mutation System (ARMS; AstraZeneca) allele-specific PCR and Scorpions (DxS) to develop assays for tumor-borne PIK3CA mutations and used real-time PCR to develop high-throughput multiplexed assays for the most commonly reported PIK3CA mutants (H1047L, H1047R, E542K, E545K). RESULTS: These assays were more sensitive than sequencing and could detect 5 copies of mutant DNA in proportions as low as 0.1% of the total DNA. We assayed DNA extracted from human tumors and detected PIK3CA mutation frequencies of 10.2% in colorectal cancer, 38.7% in breast cancer, 1.9% in lung cancer, and 2.9% in melanoma. In contrast, sequencing detected only 53% of the mutations detected by our assay. CONCLUSIONS: Multiplexed assays, which can easily be applied to clinical samples, have been developed for the detection of PIK3CA mutations. |
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