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©The Author(s) 2016.
World J Gastroenterol. Aug 21, 2016; 22(31): 7046-7057
Published online Aug 21, 2016. doi: 10.3748/wjg.v22.i31.7046
Published online Aug 21, 2016. doi: 10.3748/wjg.v22.i31.7046
Table 1 Therapeutic approach in reprogramming pancreatic ductal adenocarcinoma
Therapeutic approach | Product | Mechanism | Model studied | Ref. |
Chemical | PD325901 | Inhibits MEK1/2 in MAPK signaling | Block ADM in in vitro experiment | [16] |
Reprogram pancreatitis- induced PanIN back to acinar cells in in vivo experiment | ||||
Exendin-4 | May inhibit ERK1/2 in MAPK signaling | Reprogram PANC-1 cells back to acinar cells and endocrine cells | [82] | |
RA | Detailed study is needed | Reprogram HPAF cells to endocrine cells | [107] | |
Genetic | DKK3 knockdown | Detailed study is needed | Reprogram PANC-1 cells back to acinar cells and endocrine cells | [82] |
E47 overexpression | Functions as a sponge of ID3 to remove the inhibition of acinar transcription factors | Reprogram PDAC cell lines back to acinar cells using both in vitro and in vivo model systems | [100] |
- Citation: Wong CH, Li YJ, Chen YC. Therapeutic potential of targeting acinar cell reprogramming in pancreatic cancer. World J Gastroenterol 2016; 22(31): 7046-7057
- URL: https://www.wjgnet.com/1007-9327/full/v22/i31/7046.htm
- DOI: https://dx.doi.org/10.3748/wjg.v22.i31.7046