Ontology highlight
ABSTRACT: Background
TNBC is the most aggressive breast cancer with higher recurrence and mortality rate than other types of breast cancer. There is an urgent need for identification of therapeutic agents with unique mode of action for overcoming current challenges in TNBC treatment.Methods
Different inhibitors were used to study the cell death manner of DMOCPTL. RNA silencing was used to evaluate the functions of GPX4 in ferroptosis and apoptosis of TNBC cells and functions of EGR1 in apoptosis. Immunohistochemical assay of tissue microarray were used for investigating correlation of GPX4 and EGR1 with TNBC. Computer-aided docking and small molecule probe were used for study the binding of DMOCPTL with GPX4.Results
DMOCPTL, a derivative of natural product parthenolide, exhib
SUBMITTER: Ding Y
PROVIDER: S-EPMC7816340 | biostudies-literature | 2021 Jan
REPOSITORIES: biostudies-literature