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Antifibrotic effect via the regulation of transcription factor Sp1 in lung fibrosis.

Abstract
The aim of this study is to evaluate the antifibrotic effect of ring-type Sp1 decoy oligonucleotides (ODNs) through blocking the transcription of transforming growth factor (TGF)-beta1 and its downstream target genes. In this experiment, the expression of TGF-beta1, metalloproteinase (MMP)-13, and fibronectin was decreased in the group with the treatment of the ring-type Sp1 decoy ODNs. Also, alpha-smooth muscle actin positive bronchial lining cells and alveolar epithelial cells were observed, especially around the lesions of extracellular matrix (ECM) deposition. These findings provide evidences for the finding of pulmonary epithelial-mesenchymal transition (EMT) and the effectiveness of Sp1 transcription factor as a target for the gene therapy on lung fibrosis.
AuthorsYoon-Seup Kum, Kyung-Hyun Kim, Tae-In Park, In-Soo Suh, Hoon-Kyu Oh, Chang-Ho Cho, Jae-Bok Park, Young-Chae Chang, Ji-Hyun Park, Kwang-Gil Lee, Kwan-Kyu Park
JournalBiochemical and biophysical research communications (Biochem Biophys Res Commun) Vol. 363 Issue 2 Pg. 368-74 (Nov 16 2007) ISSN: 0006-291X [Print] United States
PMID17869213 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Oligonucleotides
  • Sp1 Transcription Factor
Topics
  • Animals
  • Gene Targeting (methods)
  • Genetic Therapy (methods)
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Oligonucleotides (administration & dosage, genetics)
  • Pulmonary Fibrosis (genetics, metabolism, therapy)
  • Sp1 Transcription Factor (genetics)
  • Treatment Outcome

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