Ontology highlight
ABSTRACT: Background
HER2-positive patients comprise approximately 20% of breast cancer cases, with HER2-targeted therapy significantly improving progression-free and overall survival. However, subsequent reprogramed tumor progression due to PI3K signaling pathway activation by PIK3CA mutations and/or PTEN-loss cause anti-HER2 resistance. Previously, alpha isoform-specific PI3K inhibitors were shown to potentiate HER2-targeted therapy in breast cancer cells carrying PI3K pathway alterations with less potent effects on PTEN-loss than PIK3CA-mutant cells. Therefore, seeking for alternative combination therapy needs urgent attentions in PTEN-loss anti-HER2 resistant breast cancer.Methods
Since remodeling of fatty acid (FA) metabolism might contribute to HER-positive breast cancer and is
SUBMITTER: Liu YY
PROVIDER: S-EPMC11806886 | biostudies-literature | 2025 Feb
REPOSITORIES: biostudies-literature