PDLIM2 repression by ROS in alveolar macrophages promotes lung tumorigenesis.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33539325.
- Also identified by DOI 10.1172/jci.insight.144394 and PMC identifier 8021114.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
One of the most fundamental and challenging questions in the field of cancer is how immunity is transformed from tumor immunosurveillance to tumor-promoting inflammation. Here, we identified the tumor suppressor PDZ-LIM domain-containing protein 2 (PDLIM2) as a checkpoint of alveolar macrophages (AMs) important for lung tumor suppression. During lung tumorigenesis, PDLIM2 expression in AMs is downregulated by ROS-activated transcription repressor BTB and CNC homology 1 (BACH1). PDLIM2 downregulation leads to constitutive activation of the transcription factor STAT3, driving AM protumorigenic polarization/activation and differentiation from monocytes attracted from the circulation to suppress cytotoxic T lymphocytes and promote lung cancer. PDLIM2 downregulation also decreases AM phagocytosis. These findings establish ROS/BACH1/PDLIM2/STAT3 as a signaling pathway driving AMs for lung tumor promotion.
Medical subject headings
- Adaptor Proteins, Signal Transducing
- LIM Domain Proteins
- Lung Neoplasms
- Macrophages
- Reactive Oxygen Species