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2000
Volume 5, Issue 12
  • ISSN: 1568-0266
  • E-ISSN: 1873-4294

Abstract

S100B interacts with the p53 protein in a calcium-dependent manner and down-regulates its function as a tumor suppressor. Therefore, inhibiting the S100B-p53 interaction represents a new approach for restoring functional wild-type p53 in cancers with elevated S100B such as found in malignant melanoma. A discussion of the biological rational for targeting S100B and a description of methodologies relevant to the discovery of compounds that inhibit S100B-p53 binding, including computational techniques, structural biology techniques, and cellular assays, is presented.

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/content/journals/ctmc/10.2174/156802605774370865
2005-10-01
2025-05-05
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