SOX2-induced IL1α-mediated immune suppression drives epithelial dysplasia malignant transformation.
Ontology highlight
ABSTRACT: Squamous cell carcinomas (SCC) are often preceded by potentially malignant precursor lesions, most of which remain benign. The terminal exhaustion phenotypes of effector T-cells and the accumulation of myeloid-derived suppressor cells (MDSC) have been thoroughly characterized in established SCC. However, it is unclear what precancerous lesions harbor a bona fide high risk for malignant transformation and how precancerous epithelial dysplasia drives the immune system to the point of no return. Here we show that expression of SRY-box transcription factor 2 (SOX2) in precancerous lesions imparts an irreversible risk that recruits suppressive myeloid cells by promoting the release of CCL2. We developed a unique genetically engineered mouse model (GEMM) to recapitulate the malignant transformat
SUBMITTER: Taner HF
PROVIDER: S-EPMC11661103 | biostudies-literature | 2024 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA