Silica induces human cyclooxygenase-2 gene expression through the NF-κB signaling pathway

Jung Kyoung Choi, Seok Geun Lee, Joo Yong Lee, Hae Yun Nam, Woon Kyu Lee, Kweon Haeng Lee, Hyung Jung Kim, Young Lim

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

Silica is a causative factor of acute cell injury in pulmonary fibrosis. Inducible cyclooxygenase-2 (COX-2) was suggested to play a role in the process of inflammation and fibrosis. We report that silica induces COX-2 expression in WI-38 fibroblasts. Further analysis showed that silica activated the transcription of COX-2 gene primarily via a nuclear factor (NF)-κB binding site in the promoter. NF-κB-inducing kinase (NIK) and TGF-κ activated kinase 1 (TAK1), the upstream signaling molecules of NF-κB, are involved in the silica-mediated COX-2 expression. The Electrophoretic Mobility Shift Assay (EMSA) showed that silica induced the direct binding of NF-κB on the putative binding site in COX-2 promoter. These results suggest that silica activates the human COX-2 gene transcription through the induction of NF-κB activity.

Original languageEnglish
Pages (from-to)163-174
Number of pages12
JournalJournal of Environmental Pathology, Toxicology and Oncology
Volume24
Issue number3
DOIs
Publication statusPublished - 2005

Keywords

  • COX-2
  • NF-κB
  • NIK
  • Pulmonary fibrosis
  • Pulmonary silicosis
  • Silica
  • TAK1

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