Inhibiting S100B restores p53 levels in primary malignant melanoma cancer cells.

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TitleInhibiting S100B restores p53 levels in primary malignant melanoma cancer cells.
Publication TypeJournal Article
Year of Publication2004
AuthorsLin, J, Yang, Q, Yan, Z, Markowitz, J, Wilder, PT, Carrier, F, Weber, DJ
JournalJ Biol Chem
Date Published2004 Aug 6
KeywordsBinding Sites, Chloramphenicol O-Acetyltransferase, DNA, Electrophoretic Mobility Shift Assay, Feedback, Physiological, Gene Expression, Gene Expression Regulation, Neoplastic, Humans, Immunosorbent Techniques, Intracellular Signaling Peptides and Proteins, Melanoma, Nerve Growth Factors, Promoter Regions, Genetic, Proteins, Recombinant Fusion Proteins, RNA, Small Interfering, S100 Proteins, Transfection, Tumor Cells, Cultured, Tumor Suppressor Protein p53

S100 calcium-binding proteins such as S100B are elevated in primary malignant melanoma and are used as markers for this and numerous other cancers. Wild-type p53 protein levels are relatively low in these cancer cells (i.e. when compared with cells without S100B) but are elevated when RNA antisense to S100B is introduced. This result implicates S100B in the down-regulation of p53 and is consistent with the large decreases in p53 protein levels observed previously in transient co-transfections of p53 and S100B (Lin, J., Blake, M., Tang, C., Zimmer, D., Rustandi, R. R., Weber, D. J., and Carrier, F. (2001) J. Biol. Chem. 276, 35037-35041). Down-regulation of p53 in primary malignant melanoma cells is likely the result of a direct interaction with S100B, which was observed by co-immunoprecipitation experiments. Furthermore, p53 binds regions of the S100B promoter, one of which matches the 20-nucleotide p53-binding consensus DNA sequence perfectly. Therefore, when p53 levels increase, it contributes to its own demise by up-regulating the transcription of S100B as part of a negative feedback loop. This is analogous to what is found for another protein that down-regulates p53, namely hdm2 (human double mutant 2).

Alternate JournalJ. Biol. Chem.
PubMed ID15178678
Grant ListGM58888 / GM / NIGMS NIH HHS / United States