Development of a multiplex allele-specific qPCR approach for testing PIK3CA mutations in patients with colorectal cancer. Issue 11 (November 2022)

• Record Type: Journal Article
• Authors: Oscorbin, Igor P.; Beginyazova, Oguljan P.; Khlistun, Inna V.; Shamovskaya, Darya V.; Oskina, Natalia A.; Filipenko, Maxim L.
• Is Part Of: Heliyon. Volume 8:Issue 11(2022)
• Publication Date: 2022-11
• Subjects: PIK3CA -- Somatic mutations -- CRC -- Multiplex amplification -- Allele-specific PCR -- ARMS; Research -- Periodicals; Medical sciences -- Periodicals; Natural history -- Periodicals; Social sciences -- Periodicals; Earth sciences -- Periodicals; Physical sciences -- Periodicals; 507.2
• DOI: 10.1016/j.heliyon.2022.e11804
• Languages: English
• ISSNs: 2405-8440

Abstract

Abstract: Phosphatidylinositol 3-kinases (PI3Ks) are lipid kinases involved in cellular growth and division. Somatic mutations in one of the PI3K catalytic subunit genes, PIK3CA, are frequently found in numerous malignancies, including colorectal cancer (CRC). Several PIK3CA inhibitors are approved for the treatment of breast cancer and lymphoma. Activating mutations in PIK3CA tend to occur in exons 9 and 20, with mutations in other exons 1, 4, and 7 being less common. Most test systems for PIK3CA mutation screening are designed to detect mutations in exons 9 and 20, leaving exons 1–7 overlooked. We have developed a multiplex AS-PCR to screen for PIK3CA mutations in exons 1, 4, 7, 9, and 20. Validation was performed on 515 CRC samples of patients from Siberia and the Far East of Russia. The assay sensitivity was 0.05–0.5% of mutant DNA, and the overall PIK3CA mutation frequency was 13.01%, with 9.32% of mutations in exon 9, 1.94% in exon 20, and 1.74% in exons 1–7. The assay designed is suitable for the analysis of activating PIK3CA mutations in formalin-fixed paraffin-embedded tissue samples. The present work is the first study characterizing the PIK3CA mutation frequency in CRC patients from the eastern part of Russia. Abstract : PIK3CA ; Somatic mutations; CRC; Multiplex amplification; Allele-specific PCR; ARMS.