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©2014 Baishideng Publishing Group Inc.
World J Gastroenterol. Jul 14, 2014; 20(26): 8471-8481
Published online Jul 14, 2014. doi: 10.3748/wjg.v20.i26.8471
Published online Jul 14, 2014. doi: 10.3748/wjg.v20.i26.8471
Figure 6 Mini-organotypic model of pancreatic ductal adenocarcinoma.
Extra cellular matrix gel is polymerised within the insert of a standard migration assay plate. A: Cancer and pancreatic stellate cells are seeded on top of the gel and allowed to attach. The media is then removed and then replaced only in the bottom of the well to again create a chemotactic gradient cells are cultured for 7-10 d; B: HE image demonstrating a similar pattern of cell proliferation and invasion is seen, as in the raised model; C: Immunofluorscence in the same gel showing strong cytokeratin expression in the cancer cells and vimentin expression in the stellate cells which form a layer below the cancer cells and invade into the gel ahead of cancer cells.
- Citation: Coleman SJ, Watt J, Arumugam P, Solaini L, Carapuca E, Ghallab M, Grose RP, Kocher HM. Pancreatic cancer organotypics: High throughput, preclinical models for pharmacological agent evaluation. World J Gastroenterol 2014; 20(26): 8471-8481
- URL: https://www.wjgnet.com/1007-9327/full/v20/i26/8471.htm
- DOI: https://dx.doi.org/10.3748/wjg.v20.i26.8471