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PRIMA-1(MET) Inhibits Growth of Mouse Tumors Carrying Mutant p53

Reactivation of the tumor suppressor activity to mutant p53 should trigger massive apoptosis and eliminate tumors. The low molecular weight compounds PRIMA-1 and the structural analog PRIMA-1(MET) reactivate human mutant p53 in vitro and suppress growth of human tumor xenografts in SCID mice. Howeve...

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Detalles Bibliográficos
Autores principales: Zache, Nicole, Lambert, Jeremy M. R., Wiman, Klas G., Bykov, Vladimir J. N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4618963/
https://www.ncbi.nlm.nih.gov/pubmed/18791272
http://dx.doi.org/10.3233/CLO-2008-0440
Descripción
Sumario:Reactivation of the tumor suppressor activity to mutant p53 should trigger massive apoptosis and eliminate tumors. The low molecular weight compounds PRIMA-1 and the structural analog PRIMA-1(MET) reactivate human mutant p53 in vitro and suppress growth of human tumor xenografts in SCID mice. However, little is known about their effect on mouse mutant p53 in mouse tumor cells. We have examined the effect of PRIMA-1(MET) on mouse sarcomas, mammary carcinomas and chemically induced fibrosarcomas. PRIMA-1(MET) showed potent growth suppression in mutant p53-carrying mouse tumors in vitro and a significant anti-tumor effect in syngeneic mice in vivo. These results demonstrate that PRIMA-1(MET) targets mouse tumors carrying mutant p53 and provide strong support for the anti-tumor efficiency of PRIMA-1(MET)in vivo.