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PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA

PIK3CA mutation is considered a good candidate for targeted therapies in cancers, especially biliary tract cancer (BTC). We evaluated the utility of cell free DNA (cfDNA) from serum by using droplet digital PCR (ddPCR) as an alternative source for PIK3CA mutation analysis. To identify matching archi...

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Autores principales: Kim, Seung Tae, Lira, Maruja, Deng, Shibing, Lee, Sujin, Park, Young Suk, Lim, Ho Yeong, Kang, Won Ki, Mao, Mao, Heo, Jin Seok, Kwon, Wooil, Jang, Kee-Taek, Lee, Jeeyun, Park, Joon Oh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741877/
https://www.ncbi.nlm.nih.gov/pubmed/26498688
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author Kim, Seung Tae
Lira, Maruja
Deng, Shibing
Lee, Sujin
Park, Young Suk
Lim, Ho Yeong
Kang, Won Ki
Mao, Mao
Heo, Jin Seok
Kwon, Wooil
Jang, Kee-Taek
Lee, Jeeyun
Park, Joon Oh
author_facet Kim, Seung Tae
Lira, Maruja
Deng, Shibing
Lee, Sujin
Park, Young Suk
Lim, Ho Yeong
Kang, Won Ki
Mao, Mao
Heo, Jin Seok
Kwon, Wooil
Jang, Kee-Taek
Lee, Jeeyun
Park, Joon Oh
author_sort Kim, Seung Tae
collection PubMed
description PIK3CA mutation is considered a good candidate for targeted therapies in cancers, especially biliary tract cancer (BTC). We evaluated the utility of cell free DNA (cfDNA) from serum by using droplet digital PCR (ddPCR) as an alternative source for PIK3CA mutation analysis. To identify matching archival tumour specimens from serum samples of advanced BTC patients, mutation detection using ddPCR with Bio-Rad's PrimePCR mutation and wild type assays were performed for PIK3CA p.E542K, p.E545K, and p.H1047R. Thirty-eight patients with metastatic BTC were enrolled. Only one (BTC 29T) sample (n = 38) was positive for PIK3CA p.E542K and another (BTC 27T) for p.H1047R mutation; none was positive for PIK3CA p.E545K. Matched serum sample (BTC 29P) was positive for PIK3CA p.E542K with 28 mutant copies detected, corresponding to 48 copies/ml of serum and an allelic prevalence of 0.3%. Another matched serum sample (BTC 27P) was positive for PIK3CA p.H1047R with 10 mutant copies detected, i.e. 18 copies/ml and an allelic frequency of 0.2%. High correlation was noted in the PIK3CA mutation status between tumour gDNA and serum cfDNA. Low-level PIK3CA mutations were detectable in the serum indicating the utility of cfDNA as a DNA source to detect cancer-derived mutations in metastatic biliary cancers.
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spelling pubmed-47418772016-03-23 PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA Kim, Seung Tae Lira, Maruja Deng, Shibing Lee, Sujin Park, Young Suk Lim, Ho Yeong Kang, Won Ki Mao, Mao Heo, Jin Seok Kwon, Wooil Jang, Kee-Taek Lee, Jeeyun Park, Joon Oh Oncotarget Research Paper PIK3CA mutation is considered a good candidate for targeted therapies in cancers, especially biliary tract cancer (BTC). We evaluated the utility of cell free DNA (cfDNA) from serum by using droplet digital PCR (ddPCR) as an alternative source for PIK3CA mutation analysis. To identify matching archival tumour specimens from serum samples of advanced BTC patients, mutation detection using ddPCR with Bio-Rad's PrimePCR mutation and wild type assays were performed for PIK3CA p.E542K, p.E545K, and p.H1047R. Thirty-eight patients with metastatic BTC were enrolled. Only one (BTC 29T) sample (n = 38) was positive for PIK3CA p.E542K and another (BTC 27T) for p.H1047R mutation; none was positive for PIK3CA p.E545K. Matched serum sample (BTC 29P) was positive for PIK3CA p.E542K with 28 mutant copies detected, corresponding to 48 copies/ml of serum and an allelic prevalence of 0.3%. Another matched serum sample (BTC 27P) was positive for PIK3CA p.H1047R with 10 mutant copies detected, i.e. 18 copies/ml and an allelic frequency of 0.2%. High correlation was noted in the PIK3CA mutation status between tumour gDNA and serum cfDNA. Low-level PIK3CA mutations were detectable in the serum indicating the utility of cfDNA as a DNA source to detect cancer-derived mutations in metastatic biliary cancers. Impact Journals LLC 2015-10-16 /pmc/articles/PMC4741877/ /pubmed/26498688 Text en Copyright: © 2015 Kim et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Paper
Kim, Seung Tae
Lira, Maruja
Deng, Shibing
Lee, Sujin
Park, Young Suk
Lim, Ho Yeong
Kang, Won Ki
Mao, Mao
Heo, Jin Seok
Kwon, Wooil
Jang, Kee-Taek
Lee, Jeeyun
Park, Joon Oh
PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA
title PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA
title_full PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA
title_fullStr PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA
title_full_unstemmed PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA
title_short PIK3CA mutation detection in metastatic biliary cancer using cell-free DNA
title_sort pik3ca mutation detection in metastatic biliary cancer using cell-free dna
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4741877/
https://www.ncbi.nlm.nih.gov/pubmed/26498688
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