Back to Search Start Over

Development of 3D-iNET ORION: a novel, pre-clinical, three-dimensional in vitro cell model for modeling human metastatic neuroendocrine tumor of the pancreas.

Authors :
Strnadel J
Valasek MA
Lin GY
Lin H
Tipps AMP
Woo SM
Fujimura K
Wang H
Choi S
Bui J
Hermosillo C
Jepsen K
Navarro MR
Kelber JA
Klemke RL
Bouvet M
Source :
Human cell [Hum Cell] 2024 Sep; Vol. 37 (5), pp. 1593-1601. Date of Electronic Publication: 2024 Aug 05.
Publication Year :
2024

Abstract

Neuroendocrine tumors (NETs) of the pancreas are rare neoplasms that present complex challenges to diagnosis and treatment due to their indolent course. The incidence of pancreatic neuroendocrine tumors has increased significantly over the past two decades. A limited number of pancreatic neuroendocrine cell lines are currently available for the research. Here, we present 3D-iNET ORION, a novel 3-dimensional (spheroid) cell line, isolated from human pancreatic neuroendocrine tumor liver metastasis. Three-dimensionally grown (3D) cancer cell lines have gained interest over the past years as 3D cancer cell lines better recapitulate the in vivo structure of tumors, and are more suitable for in vitro and in vivo experiments. 3D-iNET ORION cancer cell line showed high potential to form tumorspheres when embedded in Matrigel matrix and expresses synaptophysin and EpCAM. Electron microscopy analysis of cancer cell line proved the presence of dense neurosecretory granules. When xenografted into athymic mice, 3D-iNET ORION cells produce slow-growing tumors, positive for chromogranin and synaptophysin. Human Core Exome Panel Analysis has shown that 3DiNET ORION cell line retains the genetic aberration profile detected in the original tumor. In conclusion, our newly developed neuroendocrine cancer cell line can be considered as a new research tool for in vitro and in vivo experiments.<br /> (© 2024. The Author(s).)

Details

Language :
English
ISSN :
1749-0774
Volume :
37
Issue :
5
Database :
MEDLINE
Journal :
Human cell
Publication Type :
Academic Journal
Accession number :
39103560
Full Text :
https://doi.org/10.1007/s13577-024-01113-7