Selective chemical probe inhibitor of Stat3, identified through structure-based virtual screening, induces antitumor activity

Proc Natl Acad Sci U S A. 2007 May 1;104(18):7391-6. doi: 10.1073/pnas.0609757104. Epub 2007 Apr 26.

Abstract

S3I-201 (NSC 74859) is a chemical probe inhibitor of Stat3 activity, which was identified from the National Cancer Institute chemical libraries by using structure-based virtual screening with a computer model of the Stat3 SH2 domain bound to its Stat3 phosphotyrosine peptide derived from the x-ray crystal structure of the Stat3beta homodimer. S3I-201 inhibits Stat3.Stat3 complex formation and Stat3 DNA-binding and transcriptional activities. Furthermore, S3I-201 inhibits growth and induces apoptosis preferentially in tumor cells that contain persistently activated Stat3. Constitutively dimerized and active Stat3C and Stat3 SH2 domain rescue tumor cells from S3I-201-induced apoptosis. Finally, S3I-201 inhibits the expression of the Stat3-regulated genes encoding cyclin D1, Bcl-xL, and survivin and inhibits the growth of human breast tumors in vivo. These findings strongly suggest that the antitumor activity of S3I-201 is mediated in part through inhibition of aberrant Stat3 activation and provide the proof-of-concept for the potential clinical use of Stat3 inhibitors such as S3I-201 in tumors harboring aberrant Stat3.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aminosalicylic Acid / chemistry
  • Aminosalicylic Acid / metabolism
  • Aminosalicylic Acid / therapeutic use
  • Aminosalicylic Acids*
  • Animals
  • Antineoplastic Agents / chemistry*
  • Antineoplastic Agents / metabolism*
  • Antineoplastic Agents / therapeutic use
  • Apoptosis
  • Benzenesulfonates / chemistry*
  • Benzenesulfonates / metabolism*
  • Benzenesulfonates / therapeutic use
  • Cell Line
  • Computational Biology
  • DNA / chemistry
  • DNA / metabolism
  • Drug Evaluation, Preclinical*
  • Gene Expression Regulation
  • Humans
  • Mice
  • Models, Molecular
  • Neoplasms / drug therapy
  • Neoplasms / genetics
  • Neoplasms / metabolism
  • Neoplasms / pathology
  • Phosphotyrosine / metabolism
  • Protein Binding
  • Protein Structure, Tertiary
  • STAT3 Transcription Factor / antagonists & inhibitors
  • STAT3 Transcription Factor / chemistry*
  • STAT3 Transcription Factor / genetics
  • STAT3 Transcription Factor / metabolism*
  • Transcription, Genetic / genetics
  • Xenograft Model Antitumor Assays

Substances

  • Aminosalicylic Acids
  • Antineoplastic Agents
  • Benzenesulfonates
  • NSC 74859
  • STAT3 Transcription Factor
  • Phosphotyrosine
  • Aminosalicylic Acid
  • DNA