In vivo and in vitro propagation of intraductal papillary mucinous neoplasms

• Published in: Laboratory investigation 2010-05, Vol.90 (5), p.665-673
• Main Authors: Kamiyama, Hirohiko, Kamiyama, Mihoko, Hong, Seung-Mo, Karikari, Collins A, Lin, Ming-Tseh, Borges, Michael W, Griffith, Margaret, Young, Angela, Norris-Kirby, Alexis, Lubek, Conrad, Mizuma, Masamichi, Feldmann, Georg, Shi, Chanjuan, Liang, Hong, Goggins, Michael G, Maitra, Anirban, Hruban, Ralph H, Eshleman, James R
• Format: Article
• Language: English
• Subjects: 692/420/755; 692/699/67/1504/1713; Adenocarcinoma, Mucinous - genetics; Adenocarcinoma, Mucinous - metabolism; Adenocarcinoma, Mucinous - pathology; Adult; Aged; Aged, 80 and over; Animals; Biological and medical sciences; Biotechnology; Carcinoma, Pancreatic Ductal - genetics; Carcinoma, Pancreatic Ductal - metabolism; Carcinoma, Pancreatic Ductal - pathology; Carcinoma, Papillary - genetics; Carcinoma, Papillary - metabolism; Carcinoma, Papillary - pathology; Cell Line, Tumor; cell lines; Cyclin-Dependent Kinase Inhibitor p16 - genetics; Cyclin-Dependent Kinase Inhibitor p16 - metabolism; DNA Fingerprinting; Female; Fundamental and applied biological sciences. Psychology; Gastroenterology. Liver. Pancreas. Abdomen; Humans; immunodeficient mice; Immunohistochemistry; intraductal papillary mucinous neoplasm (IPMN); Investigative techniques, diagnostic techniques (general aspects); Laboratory Medicine; Liver. Biliary tract. Portal circulation. Exocrine pancreas; Male; Medical sciences; Medicine; Medicine & Public Health; Mice; Mice, Inbred NOD; Mice, Knockout; Mice, Nude; Mice, SCID; Middle Aged; Neoplasm Transplantation; pancreatic cancer; Pancreatic Neoplasms - genetics; Pancreatic Neoplasms - metabolism; Pancreatic Neoplasms - pathology; Pathology; precursor lesions; research-article; Transplantation, Heterologous; Tumors
• ISSN: 0023-6837; 1530-0307
• DOI: 10.1038/labinvest.2010.51

Intraductal papillary mucinous neoplasms (IPMNs) are one of the three known curable precursor lesions of invasive pancreatic ductal adenocarcinoma, an almost uniformly fatal disease. Cell lines from IPMNs and their invasive counterparts should be valuable to identify gene mutations critical to IPMN carcinogenesis, and permit high-throughput screening to identify drugs that cause regression of these lesions. To advance the study of the biological features of IPMNs, we attempted in vivo and in vitro growth of selected IPMNs based on the hypothesis that IPMNs could be grown in the most severely immunodeficient mice. We examined 14 cases by implanting them into nude, severe combined immunodeficient (SCID), and NOD/SCID/IL2Rγnull (NOG) mice, in addition to direct culture, to generate tumor xenografts and cell lines. One sample was directly cultured only. Thirteen tumors were implanted into the three types of mice, including 10 tumors implanted into the triple immunodeficient NOG mice, in which the majority (8 of 10) grew. This included five IPMNs lacking an invasive component. One of the explanted IPMNs, with an associated invasive carcinoma, was successfully established as a cell line. Tumorigenicity was confirmed by growth in soft agar, growth in immunodeficient mice, and the homozygous deletion of p16/cdkn2a. Epithelial differentiation of the cell line was documented by cytokeratin expression. Patient origin was confirmed using DNA fingerprinting. Most non-invasive IPMNs grow in NOG mice. We successfully established one IPMN cell line, and plan to use it to clarify the molecular pathogenesis of IPMNs.