Inhibition of pulmonary fibrosis with nutlin-3a and peptides
View Patent ↗In fibrotic lung fibroblasts, basal levels of p53 protein (and miR-34a) are markedly suppressed, leading to reduced p53-mediated inhibition of uPA and uPAR, or concurrent induction of PAI-1. These changes contribute to excessive FL-fibroblast proliferation and production of extracellular matrix (ECM), and, therefore, pulmonary fibrosis. These processes are reversed by treating the cells, and treating subjects suffering from idiopathic pulmonary fibrosis (IPF) with the small organic molecule nutlin-3a (NTL) or with a peptide, CSP-4 (SEQ ID NO:1), or variants or derivatives or multimers of this peptide, which increase p53 levels by inhibiting MDM2-mediated degradation of p53 protein. Use of these compounds serves as a new approach to the treatment of IPF, as they restore p53 expression and p53-mediated changes in the uPA-fibrinolytic system in FL-fibroblasts and restrict production and deposition of ECM.
1. A method of increasing p53 and/or plasminogen activator inhibitor-1 (PAI-1) levels in a subject, comprising administering an effective amount of a pharmaceutical composition comprising a recombinant polypeptide consisting of the amino acid sequence FTTFTVT (SEQ ID NO: 1) and, optionally, including 1-5 amino acids of additional sequence at the N- or C-terminus of the sequence of SEQ ID NO: 1 to the subject, wherein the optional additional sequence at the N- or C-terminus of SEQ ID NO: 1 is not a cell internalization signal, wherein the subject has an acute lung injury or a fibrotic condition.
2. The method of claim 1 , wherein the polypeptide comprises L-amino acids.
3. The method of claim 1 , wherein the polypeptide comprises at least one D-amino acid.
4. The method of claim 1 , wherein the polypeptide is capped at its N terminus.
5. The method of claim 1 , wherein the polypeptide is capped at its C terminus.
6. The method of claim 1 , wherein the composition is administered by oral, parenteral, topical, transdermal, intravaginal, intrapenile, intranasal, intrabronchial, intracranial, intraocular, intraaural or rectal administration.
7. The method of claim 1 , wherein the composition is administered intranasaly, intrabronchially, or by instillation into lungs of the subject.
8. The method of claim 1 , wherein the composition administered by injection.
9. The method of claim 1 , wherein the pharmaceutical composition is administered systemically.
10. The method of claim 3 , wherein the subject is human.
11. The method of claim 1 , wherein the subject has an acute lung injury.
12. The method of claim 1 , wherein the subject has a fibrotic condition.
13. The method of claim 12 , wherein the fibrotic condition comprises pulmonary fibrosis.
14. The method of claim 1 , wherein the subject has idiopathic pulmonary fibrosis.
15. The method of claim 1 , wherein the recombinant polypeptide consists of the amino acid sequence FTTFTVT (SEQ ID NO:1).
16. The method of claim 1 , wherein the recombinant polypeptide consists of the amino acid sequence FTTFTVT (SEQ ID NO:1) and 1-5 amino acids of additional sequence at the N-terminus.
17. The method of claim 1 , wherein the recombinant polypeptide consists of the amino acid sequence FTTFTVT (SEQ ID NO:1) and 1-5 amino acids of additional sequence at the C-terminus.