Peptide able to break the m-p53/p63, m-p53/p73 and...

Chemistry: natural resins or derivatives; peptides or proteins; – Peptides of 3 to 100 amino acid residues

Reexamination Certificate

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Details

C530S327000, C530S328000

Reexamination Certificate

active

07939624

ABSTRACT:
The object of the present invention is the identification of a group of peptides able to break the interaction between the mutated protein p53 (hereinafter m-p53) and the proteins p63, p73 and the relative isoform proteins (hereinafter p63, p73 and p-isoforms) in the m-p53/p63, m-p53/p73 and m-p53/p-isoforms proteinic complex that has formed in the nucleus of tumor cells. Furthermore, the present invention relates to a method for causing the breakage of said proteinic complexes existing in the tumor cell lines in vitro. The present invention further relates to the use of said peptides for the preparation of a pharmaceutical composition for treating human tumors.

REFERENCES:
patent: WO 97/28186 (1997-08-01), None
patent: 9851350 (1998-11-01), None
patent: WO 99/50287 (1999-10-01), None
patent: 9966946 (1999-12-01), None
patent: 03025010 (2003-03-01), None

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