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Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform

Background: To support cancer therapy, development of low cost library preparation techniques for targeted next generation sequencing (NGS) is needed. In this study we designed and tested a PCR-based library preparation panel with limited target area for sequencing the top 12 somatic mutation hot sp...

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Autores principales: Péterfia, Bálint, Kalmár, Alexandra, Patai, Árpád V., Csabai, István, Bodor, András, Micsik, Tamás, Wichmann, Barnabás, Egedi, Krisztina, Hollósi, Péter, Kovalszky, Ilona, Tulassay, Zsolt, Molnár, Béla
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Ivyspring International Publisher 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327365/
https://www.ncbi.nlm.nih.gov/pubmed/28243320
http://dx.doi.org/10.7150/jca.16037
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author Péterfia, Bálint
Kalmár, Alexandra
Patai, Árpád V.
Csabai, István
Bodor, András
Micsik, Tamás
Wichmann, Barnabás
Egedi, Krisztina
Hollósi, Péter
Kovalszky, Ilona
Tulassay, Zsolt
Molnár, Béla
author_facet Péterfia, Bálint
Kalmár, Alexandra
Patai, Árpád V.
Csabai, István
Bodor, András
Micsik, Tamás
Wichmann, Barnabás
Egedi, Krisztina
Hollósi, Péter
Kovalszky, Ilona
Tulassay, Zsolt
Molnár, Béla
author_sort Péterfia, Bálint
collection PubMed
description Background: To support cancer therapy, development of low cost library preparation techniques for targeted next generation sequencing (NGS) is needed. In this study we designed and tested a PCR-based library preparation panel with limited target area for sequencing the top 12 somatic mutation hot spots in colorectal cancer on the GS Junior instrument. Materials and Methods: A multiplex PCR panel was designed to amplify regions of mutation hot spots in 12 selected genes (APC, BRAF, CTNNB1, EGFR, FBXW7, KRAS, NRAS, MSH6, PIK3CA, SMAD2, SMAD4, TP53). Amplicons were sequenced on a GS Junior instrument using ligated and barcoded adaptors. Eight samples were sequenced in a single run. Colonic DNA samples (8 normal mucosa; 33 adenomas; 17 adenocarcinomas) as well as HT-29 and Caco-2 cell lines with known mutation profiles were analyzed. Variants found by the panel on APC, BRAF, KRAS and NRAS genes were validated by conventional sequencing. Results: In total, 34 kinds of mutations were detected including two novel mutations (FBXW7 c.1740:C>G and SMAD4 c.413C>G) that have not been recorded in mutation databases, and one potential germline mutation (APC). The most frequently mutated genes were APC, TP53 and KRAS with 30%, 15% and 21% frequencies in adenomas and 29%, 53% and 29% frequencies in carcinomas, respectively. In cell lines, all the expected mutations were detected except for one located in a homopolymer region. According to re-sequencing results sensitivity and specificity was 100% and 92% respectively. Conclusions: Our NGS-based screening panel denotes a promising step towards low cost colorectal cancer genotyping on the GS Junior instrument. Despite the relatively low coverage, we discovered two novel mutations and obtained mutation frequencies comparable to literature data. Additionally, as an advantage, this panel requires less template DNA than sequence capture colon cancer panels currently available for the GS Junior instrument.
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spelling pubmed-53273652017-02-27 Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform Péterfia, Bálint Kalmár, Alexandra Patai, Árpád V. Csabai, István Bodor, András Micsik, Tamás Wichmann, Barnabás Egedi, Krisztina Hollósi, Péter Kovalszky, Ilona Tulassay, Zsolt Molnár, Béla J Cancer Research Paper Background: To support cancer therapy, development of low cost library preparation techniques for targeted next generation sequencing (NGS) is needed. In this study we designed and tested a PCR-based library preparation panel with limited target area for sequencing the top 12 somatic mutation hot spots in colorectal cancer on the GS Junior instrument. Materials and Methods: A multiplex PCR panel was designed to amplify regions of mutation hot spots in 12 selected genes (APC, BRAF, CTNNB1, EGFR, FBXW7, KRAS, NRAS, MSH6, PIK3CA, SMAD2, SMAD4, TP53). Amplicons were sequenced on a GS Junior instrument using ligated and barcoded adaptors. Eight samples were sequenced in a single run. Colonic DNA samples (8 normal mucosa; 33 adenomas; 17 adenocarcinomas) as well as HT-29 and Caco-2 cell lines with known mutation profiles were analyzed. Variants found by the panel on APC, BRAF, KRAS and NRAS genes were validated by conventional sequencing. Results: In total, 34 kinds of mutations were detected including two novel mutations (FBXW7 c.1740:C>G and SMAD4 c.413C>G) that have not been recorded in mutation databases, and one potential germline mutation (APC). The most frequently mutated genes were APC, TP53 and KRAS with 30%, 15% and 21% frequencies in adenomas and 29%, 53% and 29% frequencies in carcinomas, respectively. In cell lines, all the expected mutations were detected except for one located in a homopolymer region. According to re-sequencing results sensitivity and specificity was 100% and 92% respectively. Conclusions: Our NGS-based screening panel denotes a promising step towards low cost colorectal cancer genotyping on the GS Junior instrument. Despite the relatively low coverage, we discovered two novel mutations and obtained mutation frequencies comparable to literature data. Additionally, as an advantage, this panel requires less template DNA than sequence capture colon cancer panels currently available for the GS Junior instrument. Ivyspring International Publisher 2017-01-12 /pmc/articles/PMC5327365/ /pubmed/28243320 http://dx.doi.org/10.7150/jca.16037 Text en © Ivyspring International Publisher This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
spellingShingle Research Paper
Péterfia, Bálint
Kalmár, Alexandra
Patai, Árpád V.
Csabai, István
Bodor, András
Micsik, Tamás
Wichmann, Barnabás
Egedi, Krisztina
Hollósi, Péter
Kovalszky, Ilona
Tulassay, Zsolt
Molnár, Béla
Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform
title Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform
title_full Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform
title_fullStr Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform
title_full_unstemmed Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform
title_short Construction of a multiplex mutation hot spot PCR panel: the first step towards colorectal cancer genotyping on the GS Junior platform
title_sort construction of a multiplex mutation hot spot pcr panel: the first step towards colorectal cancer genotyping on the gs junior platform
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5327365/
https://www.ncbi.nlm.nih.gov/pubmed/28243320
http://dx.doi.org/10.7150/jca.16037
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