CFTR chloride channel drug discovery - Inhibitors as antidiarrheals and activators for therapy and cystic fibrosis

A. S. Verkman, Gergely L. Lukacs, Luis J V Galietta

Research output: Contribution to journalArticlepeer-review

Abstract

The Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) is a cAMP-activated chloride channel expressed in epithelia in the lung, intestine, pancreas, testis and other tissues, where it facilitates transepithelial fluid transport. In the intestine CFTR provides the major route for chloride secretion in certain diarrheas. Mutations in CFTR cause the hereditary disease cystic fibrosis, where chronic lung infection and deterioration in lung function cause early death. CFTR is a well-validated targeted for development of inhibitors for therapy of secretory diarrheas and activators for therapy in cystic fibrosis. Our lab has identified and optimized small molecule inhibitors of CFTR, as well as activators of ΔF508-CFTR, the most common mutant CFTR causing cystic fibrosis. High-throughput screening of small molecule collections utilizing a cell-based fluorescence assay of halide transport yielded thiazolidinone and glycine hydrazide CFTR inhibitors that block enterotoxin-mediated secretory diarrhea in rodent models, including a class of non-absorbable inhibitors that target the CFTR pore at its external entrance. Benzothiophene, phenylglycine and sulfonamide potentiators were identified that correct the defective gating of ΔF508-CFTR chloride channels, and other small molecules that correct its defective cellular processing. Small molecule modulators of CFTR function may be useful in the treatment of cystic fibrosis, secretory diarrhea and polycystic kidney disease.

Original languageEnglish
Pages (from-to)2235-2247
Number of pages13
JournalCurrent Pharmaceutical Design
Volume12
Issue number18
DOIs
Publication statusPublished - Jun 2006

Keywords

  • CFTR
  • Chloride channel
  • Cystic fibrosis
  • Diarrhea
  • Drug discovery
  • High-throughput screening
  • Inhibitor
  • Polycystic kidney disease

ASJC Scopus subject areas

  • Molecular Medicine
  • Pharmacology, Toxicology and Pharmaceutics(all)

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