Establishment and characterization of a new human acinar cell carcinoma cell line, Faraz-ICR, from pancreas

被引:4
作者
Rezaei, Marzieh [1 ,2 ]
Hosseini, Ahmad [2 ]
Nikeghbalian, Saman [3 ]
Ghaderi, Abbas [1 ,2 ]
机构
[1] Shiraz Univ Med Sci, Sch Med, Dept Immunol, Shiraz, Iran
[2] Shiraz Univ Med Sci, Sch Med, Shiraz Inst Canc Res, Shiraz, Iran
[3] Shiraz Univ Med Sci, Nemazee Hosp, Dept Surg, Shiraz, Iran
关键词
Acinar cell carcinoma; Cell line; Pancreatic cancer; CANCER STATISTICS; ADENOCARCINOMA; EXPRESSION; NESTIN; DIFFERENTIATION; MIGRATION; MEMBRANE; PROTEINS; INVASION; MARKERS;
D O I
10.1016/j.pan.2017.02.003
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Objectives: Basic research in the field of acinar cell carcinoma (ACC) as a rare neoplasm of the pancreas is dependent on the availability of pragmatic model such as new pancreatic cancer cell lines. Thus, establishment and characterization of new pancreatic cancer cell lines from ACC origin are deemed important. Methods: Faraz-ICR cell line was derived from a 58-years old woman with pancreatic acinar cell carcinoma by the collagenase digestion protocol. We characterized the cell line by examining its morphology and cytostructural and functional profile. Results: Faraz-ICR has a doubling time of 35 hours and grows in soft agar with a colony-forming efficiency of 25%. The cell had nearly normal pattern of chromosomes in karyotype analysis and Comparative Genomic Hybridization (CGH) array analysis. Evaluation of cells by flowcytometry showed that Faraz-ICR is negative for EpCAM and mesenchymal markers in different passages, and has epithelial nature. Immunofluorescence staining revealed that cells were strongly positive for vimentin, desmin, ezrin, S100, nestin and they were negative for pan-cytokeratins, chromogranin and alpha smooth muscle actin. Conclusions: We were able to establish a new pancreatic carcinoma cell line with partial aspects of Epithelial-mesenchymal transition and aggressiveness. This cell line might be suitable for studying various anticancer drugs and protein profile aiming to see any possible tumor associated marker for ACC. (C) 2017 IAP and EPC. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:303 / 309
页数:7
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