PDLIM2 repression by ROS in alveolar macrophages promotes lung tumorigenesis

JCI Insight. 2021 Mar 8;6(5):e144394. doi: 10.1172/jci.insight.144394.

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.

Keywords: Cancer; Lung cancer; Macrophages; Oncology.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Basic-Leucine Zipper Transcription Factors / metabolism
  • Bone Marrow Cells / cytology
  • Bone Marrow Cells / metabolism
  • Cells, Cultured
  • LIM Domain Proteins / metabolism*
  • Lung Neoplasms / metabolism*
  • Macrophages / cytology
  • Macrophages / metabolism*
  • Mice
  • Monocytes / cytology
  • Monocytes / metabolism
  • Reactive Oxygen Species / metabolism*
  • STAT3 Transcription Factor / metabolism

Substances

  • Adaptor Proteins, Signal Transducing
  • Bach1 protein, mouse
  • Basic-Leucine Zipper Transcription Factors
  • LIM Domain Proteins
  • Pdlim2 protein, mouse
  • Reactive Oxygen Species
  • STAT3 Transcription Factor
  • Stat3 protein, mouse