Ontology highlight
ABSTRACT: Background
Claudin-4 (CLDN4), a tight junction protein, is overexpressed in several types of cancer, and is considered a biomarker for cancer-targeted treatment. CLDN4 is not exposed in normal cells, but becomes accessible in cancer cells, in which tight junctions are weakened. Notably, surface-exposed CLDN4 has recently been found to act as a receptor for Clostridium perfringens enterotoxin (CPE) and fragment of CPE (CPE17) that binds to the second domain of CLDN4.Methods
Here, we sought to develop a CPE17-containing liposome that targets pancreatic cancers through binding to exposed CLDN4.Results
Doxorubicin (Dox)-loaded, CPE17-conjugated liposomes (D@C-LPs) preferentially targeted CLDN4-expressing cell lines, as evidenced by greater uptake and cytotoxicity compar
SUBMITTER: Bang C
PROVIDER: S-EPMC10214683 | biostudies-literature | 2023 May
REPOSITORIES: biostudies-literature