Multiplexed Assays for Detection of Mutations in PIK3CA

Author:

Board Ruth E123,Thelwell Nicola J4,Ravetto Paul F4,Little Stephen4,Ranson Malcolm2,Dive Caroline3,Hughes Andrew1,Whitcombe David4

Affiliation:

1. Discovery Medicine, AstraZeneca Pharmaceuticals, Macclesfield, UK

2. CRUK Department of Medical Oncology, Christie Hospital NHS Trust, Manchester, UK

3. Clinical and Experimental Pharmacology Group, Paterson Institute of Cancer Research, University of Manchester, Manchester, UK

4. DxS Ltd, Manchester, UK

Abstract

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.

Funder

Cancer Research UK

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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