Transcriptional inhibition of progressive renal disease by gene silencing pyrrole–imidazole polyamide targeting of the transforming growth factor-β1 promoter
Author(s) -
Hiroyuki Matsuda,
Noboru Fukuda,
Takahiro Ueno,
Mayumi Katakawa,
Xiaofei Wang,
Takayoshi Watanabe,
Seiichi Matsui,
Takahiko Aoyama,
Kosuke Saito,
Toshikazu Bando,
Yoshiaki Matsumoto,
Hiroaki Nagase,
Koichi Matsumoto,
Hiroshi Sugiyama
Publication year - 2010
Publication title -
kidney international
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.499
H-Index - 276
eISSN - 1523-1755
pISSN - 0085-2538
DOI - 10.1038/ki.2010.330
Subject(s) - gene silencing , cancer research , transforming growth factor , growth factor , promoter , gene , imidazole , chemistry , microbiology and biotechnology , biology , gene expression , receptor , biochemistry
Pyrrole-imidazole (PI) polyamides are small synthetic molecules that recognize and attach to the minor groove of DNA, thereby inhibiting gene transcription by blocking transcription factor binding. These derivatives can act as gene silencers inhibiting target gene expression under stimulatory conditions such as disease. To evaluate PI polyamides as treatments for the progression of renal diseases, we examined morphological effects, pharmacological properties, and the specificity of PI polyamides targeted to the transforming growth factor (TGF)-β1 promoter during salt-induced hypertensive nephrosclerosis in Dahl salt-sensitive rats. The targeted PI polyamide markedly reduced glomerulosclerosis and interstitial fibrosis without side effects. PI polyamide significantly decreased expression of TGF-β1 and extracellular matrix in the renal cortex. Microarray analysis found that only 3% of the transcripts were affected by PI polyamide, but this included decreased expression of extracellular matrix, TGF-β1-related cytokines, angiogenic, and cell stabilizing factors, proteinases, and renal injury-related factors. Thus, targeted PI polyamides are potential gene silencers for diseases not treatable by current remedies.
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