1. Mutational Patterns in Pancreatic Juice of Intraductal Papillary Mucinous Neoplasms and Concomitant Pancreatic Cancer
- Author
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Yoshimitsu Fukasawa, Hiroshi Hayakawa, Makoto Kadokura, Shinichi Takano, Jun Itakura, Nobuyuki Enomoto, Daisuke Ichikawa, Sumio Hirose, Tadashi Sato, Hiroshi Kono, Ei Takahashi, Mitsuharu Fukasawa, Hiroko Shindo, Satoshi Kawakami, Hiromichi Kawaida, Kunio Mochizuki, and Shinya Maekawa
- Subjects
Pathology ,medicine.medical_specialty ,endocrine system diseases ,Endocrinology, Diabetes and Metabolism ,Proto-Oncogene Proteins p21(ras) ,03 medical and health sciences ,0302 clinical medicine ,Endocrinology ,Pancreatic Juice ,Pancreatic cancer ,Biomarkers, Tumor ,Internal Medicine ,medicine ,Carcinoma ,Humans ,Pancreatic carcinoma ,Aged ,Aged, 80 and over ,Hepatology ,Intraductal papillary mucinous neoplasm ,business.industry ,High-Throughput Nucleotide Sequencing ,Middle Aged ,medicine.disease ,Adenocarcinoma, Mucinous ,Carcinoma, Papillary ,Pancreatic Neoplasms ,030220 oncology & carcinogenesis ,Concomitant ,Mutation ,Pancreatic juice ,Adenocarcinoma ,030211 gastroenterology & hepatology ,Tumor Suppressor Protein p53 ,business ,Carcinoma, Pancreatic Ductal - Abstract
The aims of this study were to identify genetic characteristics of intraductal papillary mucinous neoplasm (IPMN)-associated pancreatic ductal carcinoma (PDC) and to detect these markers using pancreatic juice.From 76 cases, 102 tissues were obtained: 29 cases were noninvasive IPMN, 18 were PDC derived from IPMN (D-PDC; noninvasive part, n = 16; invasive part, n = 18), and 29 were PDC concomitant with IPMN (C-PDC; IPMN part, n = 10; PDC part, n = 29). Moreover, pancreatic juice samples from 28 cases were obtained (noninvasive IPMN, n = 13; D-PDC, n = 7; C-PDC, n = 8). Fifty-one cancer-related genes were analyzed by next-generation sequencing.TP53 mutation rates in D-PDC, C-PDC, and noninvasive IPMN were 67%, 66%, and 10%, respectively. Moreover, KRAS mutational patterns between 2 simultaneous tumors differed in 1 (6.3%) of the 16 D-PDC cases and in 8 (80%) of the 10 C-PDC cases (P = 0.0006). TP53 or multiple KRAS mutations were detected using pancreatic juice more frequently in C-PDC cases than in noninvasive IPMN cases (75% and 23%, respectively, P = 0.03).Multiple KRAS mutations along with TP53 mutation are genetic markers for C-PDC, which could be detected using pancreatic juice preoperatively.
- Published
- 2019
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