| Literature DB >> 35550115 |
Yuebo Zhang1, Yong Ma2, Ying Wang3, Debabrata Mukhopadhyay4, Yan Bi5, Baoan Ji6.
Abstract
Pancreatic ductal adenocarcinoma (PDAC) is notorious for high mortality due to limited options of appropriate chemotherapy drugs. Here we report that Aurora kinase-A expression is elevated in both human and mouse PDAC samples. MLN8237, an inhibitor of Aurora kinase-A, efficiently reduced the proliferation and motility of PDAC cells in vitro as well as tumor growth in orthotropic xenograft model and genetic pancreatic cancer animal models (p53/LSL/Pdx-Cre mice) in vivo. MLN8237 exhibited tumor inhibitory effect through inhibiting proliferation and migration, and inducing apoptosis and senescence. These results provide the molecular basis for a novel chemotherapy strategy for PDAC patients.Entities:
Keywords: Apoptosis; Aurora kinase; Pancreatic cancer; Senescence; Xenograft
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Year: 2022 PMID: 35550115 PMCID: PMC9189053 DOI: 10.1016/j.pan.2022.03.019
Source DB: PubMed Journal: Pancreatology ISSN: 1424-3903 Impact factor: 3.977