1. Academic Validation
  2. Identification of small-molecule inhibitors of the human S100B-p53 interaction and evaluation of their activity in human melanoma cells

Identification of small-molecule inhibitors of the human S100B-p53 interaction and evaluation of their activity in human melanoma cells

  • Bioorg Med Chem. 2013 Mar 1;21(5):1109-15. doi: 10.1016/j.bmc.2012.12.042.
Chihoko Yoshimura 1 Takamitsu Miyafusa Kouhei Tsumoto
Affiliations

Affiliation

  • 1 Medical Proteomics Laboratory, Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Abstract

The interaction between human S100 calcium-binding protein B (S100B) and the tumor suppressor protein p53 is considered to be a possible therapeutic target for malignant melanoma. To identify potent inhibitors of this interaction, we screened a fragment library of compounds by means of a fluorescence-based competition assay involving the S100B-binding C-terminal peptide of p53. Using active compounds from the fragment library as query compounds, we constructed a focused library by means of two-dimensional similarity searching of a large database. This simple, unbiased method allowed us to identify several inhibitors of the S100B-p53 interaction, and we elucidated preliminary structure-activity relationships. One of the identified compounds had the potential to inhibit the S100B-p53 interaction in melanoma cells.

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