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Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms

OBJECTIVE: Secretin-stimulated pancreatic juice contains DNA shed from cells lining the pancreatic ducts. Genetic analysis of this fluid may form a test to detect pancreatic ductal neoplasia. DESIGN: We employed digital next-generation sequencing (‘digital NGS’) to detect low-abundance mutations in...

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Autores principales: Yu, Jun, Sadakari, Yoshihiko, Shindo, Koji, Suenaga, Masaya, Brant, Aaron, Almario, Jose Alejandro Navarro, Borges, Michael, Barkley, Thomas, Fesharakizadeh, Shahriar, Ford, Madeline, Hruban, Ralph H, Shin, Eun Ji, Lennon, Anne Marie, Canto, Marcia Irene, Goggins, Michael
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243915/
https://www.ncbi.nlm.nih.gov/pubmed/27432539
http://dx.doi.org/10.1136/gutjnl-2015-311166
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author Yu, Jun
Sadakari, Yoshihiko
Shindo, Koji
Suenaga, Masaya
Brant, Aaron
Almario, Jose Alejandro Navarro
Borges, Michael
Barkley, Thomas
Fesharakizadeh, Shahriar
Ford, Madeline
Hruban, Ralph H
Shin, Eun Ji
Lennon, Anne Marie
Canto, Marcia Irene
Goggins, Michael
author_facet Yu, Jun
Sadakari, Yoshihiko
Shindo, Koji
Suenaga, Masaya
Brant, Aaron
Almario, Jose Alejandro Navarro
Borges, Michael
Barkley, Thomas
Fesharakizadeh, Shahriar
Ford, Madeline
Hruban, Ralph H
Shin, Eun Ji
Lennon, Anne Marie
Canto, Marcia Irene
Goggins, Michael
author_sort Yu, Jun
collection PubMed
description OBJECTIVE: Secretin-stimulated pancreatic juice contains DNA shed from cells lining the pancreatic ducts. Genetic analysis of this fluid may form a test to detect pancreatic ductal neoplasia. DESIGN: We employed digital next-generation sequencing (‘digital NGS’) to detect low-abundance mutations in secretin-stimulated juice samples collected from the duodenum of subjects enrolled in Cancer of the Pancreas Screening studies at Johns Hopkins Hospital. For each juice sample, digital NGS necessitated 96 NGS reactions sequencing nine genes. The study population included 115 subjects (53 discovery, 62 validation) (1) with pancreatic ductal adenocarcinoma (PDAC), (2) intraductal papillary mucinous neoplasm (IPMN), (3) controls with non-suspicious pancreata. RESULTS: Cases with PDAC and IPMN were more likely to have mutant DNA detected in pancreatic juice than controls (both p<0.0001); mutant DNA concentrations were higher in patients with PDAC than IPMN (p=0.003) or controls (p<0.001). TP53 and/or SMAD4 mutations were commonly detected in juice samples from patients with PDAC and were not detected in controls (p<0.0001); mutant TP53/SMAD4 concentrations could distinguish PDAC from IPMN cases with 32.4% sensitivity, 100% specificity (area under the curve, AUC 0.73, p=0.0002) and controls (AUC 0.82, p<0.0001). Two of four patients who developed pancreatic cancer despite close surveillance had SMAD4/TP53 mutations from their cancer detected in juice samples collected over 1 year prior to their pancreatic cancer diagnosis when no suspicious pancreatic lesions were detected by imaging. CONCLUSIONS: The detection in pancreatic juice of mutations important for the progression of low-grade dysplasia to high-grade dysplasia and invasive pancreatic cancer may improve the management of patients undergoing pancreatic screening and surveillance.
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spelling pubmed-52439152017-08-28 Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms Yu, Jun Sadakari, Yoshihiko Shindo, Koji Suenaga, Masaya Brant, Aaron Almario, Jose Alejandro Navarro Borges, Michael Barkley, Thomas Fesharakizadeh, Shahriar Ford, Madeline Hruban, Ralph H Shin, Eun Ji Lennon, Anne Marie Canto, Marcia Irene Goggins, Michael Gut Pancreas OBJECTIVE: Secretin-stimulated pancreatic juice contains DNA shed from cells lining the pancreatic ducts. Genetic analysis of this fluid may form a test to detect pancreatic ductal neoplasia. DESIGN: We employed digital next-generation sequencing (‘digital NGS’) to detect low-abundance mutations in secretin-stimulated juice samples collected from the duodenum of subjects enrolled in Cancer of the Pancreas Screening studies at Johns Hopkins Hospital. For each juice sample, digital NGS necessitated 96 NGS reactions sequencing nine genes. The study population included 115 subjects (53 discovery, 62 validation) (1) with pancreatic ductal adenocarcinoma (PDAC), (2) intraductal papillary mucinous neoplasm (IPMN), (3) controls with non-suspicious pancreata. RESULTS: Cases with PDAC and IPMN were more likely to have mutant DNA detected in pancreatic juice than controls (both p<0.0001); mutant DNA concentrations were higher in patients with PDAC than IPMN (p=0.003) or controls (p<0.001). TP53 and/or SMAD4 mutations were commonly detected in juice samples from patients with PDAC and were not detected in controls (p<0.0001); mutant TP53/SMAD4 concentrations could distinguish PDAC from IPMN cases with 32.4% sensitivity, 100% specificity (area under the curve, AUC 0.73, p=0.0002) and controls (AUC 0.82, p<0.0001). Two of four patients who developed pancreatic cancer despite close surveillance had SMAD4/TP53 mutations from their cancer detected in juice samples collected over 1 year prior to their pancreatic cancer diagnosis when no suspicious pancreatic lesions were detected by imaging. CONCLUSIONS: The detection in pancreatic juice of mutations important for the progression of low-grade dysplasia to high-grade dysplasia and invasive pancreatic cancer may improve the management of patients undergoing pancreatic screening and surveillance. BMJ Publishing Group 2017-09 2016-07-18 /pmc/articles/PMC5243915/ /pubmed/27432539 http://dx.doi.org/10.1136/gutjnl-2015-311166 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Pancreas
Yu, Jun
Sadakari, Yoshihiko
Shindo, Koji
Suenaga, Masaya
Brant, Aaron
Almario, Jose Alejandro Navarro
Borges, Michael
Barkley, Thomas
Fesharakizadeh, Shahriar
Ford, Madeline
Hruban, Ralph H
Shin, Eun Ji
Lennon, Anne Marie
Canto, Marcia Irene
Goggins, Michael
Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
title Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
title_full Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
title_fullStr Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
title_full_unstemmed Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
title_short Digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
title_sort digital next-generation sequencing identifies low-abundance mutations in pancreatic juice samples collected from the duodenum of patients with pancreatic cancer and intraductal papillary mucinous neoplasms
topic Pancreas
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5243915/
https://www.ncbi.nlm.nih.gov/pubmed/27432539
http://dx.doi.org/10.1136/gutjnl-2015-311166
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