| Literature DB >> 33713738 |
Xianze Wang1, Hao Chen2, Rui Jiang2, Xiafei Hong2, Junya Peng3, Wenyan Chen4, Jialin Jiang2, Jie Li4, Dan Huang3, Hongmei Dai2, Wenze Wang5, Junliang Lu5, Yupei Zhao6, Wenming Wu7.
Abstract
Interleukin (IL)-17 is a prominent cytokine that promotes pancreatic intraepithelial neoplasia (PanIN) and pancreatic ductal adenocarcinoma (PDAC) and is associated with the oncogenic pathways in tumor progression. However, the mechanism and therapeutic value of the IL-17 axis remain unclear. In this study, we verified the activation of the IL-17 and Notch pathways in PanIN/PDAC via complementary approaches and validated their pro-tumor effects on tumor progression. Additionally, we found a positive correlation between IL-17 and Notch; the IL-17 axis can upregulate Notch activity via the canonical NF-κB pathway in vitro, thus synergistically promoting PanIN/PDAC. Furthermore, we observed that the co-inhibition of IL-17 and the Notch pathway can enhance the therapeutic effect by restricting tumor growth in vivo. Our study highlights the synergistic effect of the IL-17 axis and Notch pathway in promoting PanIN/PDAC and further suggests that IL-17-Notch co-inhibition is a novel therapeutic strategy with superior potential in treating PDAC.Entities:
Keywords: Co-inhibition; Combination therapy; NF-κB; Pancreatic cancer; Synergy
Year: 2021 PMID: 33713738 DOI: 10.1016/j.canlet.2021.03.003
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679