Ontology highlight
ABSTRACT: Background
Targeting PLK1 has recently been proven as a viable therapeutic strategy against oesophageal squamous cell carcinom (ESCC). Therefore, this study aimed to explore whether the PLK1 inhibitor BI2536 is able to sensitize ESCC cells to cisplatin (DDP) and determine the underlying mechanisms.Methods
Viability, clonogenicity, cell cycle distribution and apoptosis were assessed in ESCC cells treated with BI2536 or DDP alone or in combination. Checkpoint activation was examined by immunoblotting and immunohistochemistry. Xenograft model was used to assess the efficacy of the co-treatment. The expression level of GSDME in tissue samples were examined by immunohistochemistry.Findings
We found that the combination of BI2536 and DDP was synergistic in ESCC cells, whi
SUBMITTER: Wu M
PROVIDER: S-EPMC6442225 | biostudies-literature | 2019 Mar
REPOSITORIES: biostudies-literature