Ontology highlight
ABSTRACT: Background
Gastric cancer is the leading cause of cancer related death worldwide. Radiation alone or combined with chemotherapy plays important role in locally advanced and metastatic gastric adenocarcinoma. MDM2-p53 interaction and downstream signaling affect cellular response to DNA damage which leads to cell cycle arrest and apoptosis. Therefore, restoring p53 function by inhibiting its interaction with MDM2 is a promising therapeutic strategy for cancer. APG-115 is a novel small molecule inhibitor which blocks the interaction of MDM2 and p53. In this study, we investigated that the radiosensitivity of APG-115 in gastric adenocarcinoma in vitro and in vivo.Methods
The role of APG-115 in six gastric cancer cells viability in vitro was determined by CCK-8 assay. The expres
SUBMITTER: Yi H
PROVIDER: S-EPMC5930807 | biostudies-literature | 2018 May
REPOSITORIES: biostudies-literature