Ontology highlight
ABSTRACT: Background
Tumor-associated macrophages (TAMs), particularly M2-polarized TAMs, are significant contributors to tumor progression, immune evasion, and therapy resistance in gastric cancer (GC). Despite efforts to target TAM recruitment or depletion, clinical efficacy remains limited. Consequently, the identification of targets that specifically inhibit or reprogram M2-polarized TAMs presents a promising therapeutic strategy.Objective
This study aims to identify a dual-function target in GC cells that drives both malignant phenotypes and M2 macrophage polarization, revealing its molecular mechanisms to provide novel therapeutic targets for selectivly targeting M2-polarized TAMs in GC.Methods
Transcriptomic and clinical data from GC and adjacent tissues were utilized
SUBMITTER: Ye Z
PROVIDER: S-EPMC11694445 | biostudies-literature | 2025 Jan
REPOSITORIES: biostudies-literature