Alteration of SHP-1/p-STAT3 Signaling: A Potential Target for Anticancer Therapy

Int J Mol Sci. 2017 Jun 8;18(6):1234. doi: 10.3390/ijms18061234.

Abstract

The Src homology 2 (SH2) domain-containing protein tyrosine phosphatase 1 (SHP-1), a non-receptor protein tyrosine phosphatase, has been reported as a negative regulator of phosphorylated signal transducer and activator of transcription 3 (STAT3) and linked to tumor development. In this present review, we will discuss the importance and function of SHP-1/p-STAT3 signaling in nonmalignant conditions as well as malignancies, its cross-talk with other pathways, the current clinical development and the potential role of inhibitors of this pathway in anticancer therapy and clinical relevance of SHP-1/p-STAT3 in cancers. Lastly, we will summarize and highlight work involving novel drugs/compounds targeting SHP-1/p-STAT3 signaling and combined strategies that were/are discovered in our and our colleagues' laboratories.

Keywords: SHP-1 (SH2 domain-containing protein tyrosine phosphatase-1); STAT3 (signal transducer and activator of transcription 3); cancer therapy.

Publication types

  • Review

MeSH terms

  • Animals
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Humans
  • Molecular Targeted Therapy
  • Neoplasms / drug therapy
  • Neoplasms / metabolism*
  • Neoplasms / pathology
  • Phosphorylation
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6 / antagonists & inhibitors
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6 / metabolism*
  • STAT3 Transcription Factor / metabolism*
  • Signal Transduction* / drug effects

Substances

  • Antineoplastic Agents
  • STAT3 Transcription Factor
  • Protein Tyrosine Phosphatase, Non-Receptor Type 6