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dc.contributor.authorBoard, Ruth E
dc.contributor.authorThelwell, Nicola J
dc.contributor.authorRavetto, Paul F
dc.contributor.authorLittle, Stephen
dc.contributor.authorRanson, Malcolm R
dc.contributor.authorDive, Caroline
dc.contributor.authorHughes, Andrew
dc.contributor.authorWhitcombe, David
dc.date.accessioned2009-04-21T16:41:15Z
dc.date.available2009-04-21T16:41:15Z
dc.date.issued2008-04
dc.identifier.citationMultiplexed assays for detection of mutations in PIK3CA. 2008, 54 (4):757-60 Clin. Chem.en
dc.identifier.issn0009-9147
dc.identifier.pmid18375489
dc.identifier.doi10.1373/clinchem.2007.098376
dc.identifier.urihttp://hdl.handle.net/10541/65741
dc.description.abstractBACKGROUND: 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.isoenen
dc.subjectBreast Canceren
dc.subjectLung Canceren
dc.subjectColorectal Canceren
dc.subjectPIK3CAen
dc.subjectTumour Markersen
dc.subject.mesh1-Phosphatidylinositol 3-Kinase
dc.subject.meshBreast Neoplasms
dc.subject.meshColorectal Neoplasms
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshLung Neoplasms
dc.subject.meshMelanoma
dc.subject.meshMutation
dc.subject.meshPolymerase Chain Reaction
dc.subject.meshSensitivity and Specificity
dc.subject.meshTumor Markers, Biological
dc.titleMultiplexed assays for detection of mutations in PIK3CA.en
dc.typeArticleen
dc.contributor.departmentDiscovery Medicine, AstraZeneca Pharmaceuticals, Macclesfield, UK. ruth.board@astrazeneca.comen
dc.identifier.journalClinical Chemistryen
html.description.abstractBACKGROUND: 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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