4.7 Article

Targeting Oncogenic Src Homology 2 Domain-Containing Phosphatase 2 (SHP2) by Inhibiting Its Protein-Protein Interactions

Journal

JOURNAL OF MEDICINAL CHEMISTRY
Volume 64, Issue 21, Pages 15973-15990

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jmedchem.1c01371

Keywords

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Funding

  1. AIRC Foundation for Cancer Research in Italy [IG19171, IG24940, IG21614]
  2. Italian Ministry of Education, University and Research (MIUR) [PRIN 20157WW5EH_007]
  3. Regione Lazio [A03752020-36719]
  4. Italian Ministry of Health
  5. Partnership for Advanced Computing in Europe (PRACE) [2019204928, 2017174118]
  6. CINECA [HP10BL5G4C]
  7. AIRC research fellowship
  8. European Program on Rare Diseases (NSEuroNet)

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A new class of inhibitors targeting protein-protein interactions of the SHP2 phosphatase were developed, showing potential for cancer and rare disease therapy. These inhibitors exhibit high affinity and selectivity, with stronger affinity for pathogenic SHP2 mutants. The best peptide inhibitor demonstrated promising effects in zebrafish embryos, indicating a novel route for SHP2-targeted therapies and further research into protein-protein interactions in SHP2 function.
We developed a new class of inhibitors of protein-protein interactions of the SHP2 phosphatase, which is pivotal in cell signaling and represents a central target in the therapy of cancer and rare diseases. Currently available SHP2 inhibitors target the catalytic site or an allosteric pocket but lack specificity or are ineffective for disease-associated SHP2 mutants. Considering that pathogenic lesions cause signaling hyperactivation due to increased levels of SHP2 association with cognate proteins, we developed peptide-based molecules with nanomolar affinity for the N-terminal Src homology domain of SHP2, good selectivity, stability to degradation, and an affinity for pathogenic variants of SHP2 that is 2-20 times higher than for the wild-type protein. The best peptide reverted the effects of a pathogenic variant (D61G) in zebrafish embryos. Our results provide a novel route for SHP2-targeted therapies and a tool for investigating the role of protein-protein interactions in the function of SHP2.

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