Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/56853
Title: The Ig V-H complementarity-determining region 3-containing Rb9 peptide, inhibits melanoma cells migration and invasion by interactions with Hsp90 and an adhesion G-protein coupled receptor
Authors: Girola, Natalia [UNIFESP]
Matsuo, Alisson Leonardo [UNIFESP]
Figueiredo, Carlos Rogerio [UNIFESP]
Massaoka, Mariana Hiromi [UNIFESP]
Farias, Camyla Fernandez de [UNIFESP]
Arruda, Denise C.
Azevedo, Ricardo A.
Monteiro, Hugo Pequeno [UNIFESP]
Resende-Lara, Pedro T.
Cunha, Rodrigo L. O. R.
Polonelli, Luciano
Travassos, Luiz Rodolpho [UNIFESP]
Keywords: Antitumor peptides
Antibody CDRs
Melanoma
Cell migration
Metastasis
Hsp90
G-protein coupled receptor
Issue Date: 2016
Publisher: Elsevier Science Inc
Citation: Peptides. New York, v. 85, p. 1-15, 2016.
Abstract: The present work aims at investigating the mechanism of action of the Rb9 peptide, which contains the VHCDR 3 sequence of anti-sodium-dependent phosphate transport protein 2B (NaPi2B) monoclonal antibody RebMab200 and displayed antitumor properties. Short peptides corresponding to the hyper variable complementarity-determining regions (CDRs) of immunoglobulins have been associated with antimicrobial, antiviral, immunomodulatory and antitumor activities regardless of the specificity of the antibody. We have shown that the CDR derived peptide Rb9 induced substrate hyperadherence, inhibition of cell migration and matrix invasion in melanoma and other tumor cell lines. Rb9 also inhibited metastasis of murine melanoma in a syngeneic mouse model. We found that Rb9 binds to and interferes with Hsp90 chaperone activity causing attenuation of FAK-Src signaling and downregulation of active Rac1 in B16F10-Next melanoma cells. The peptide also bound to an adhesion G-protein coupled receptor, triggering a concentration-dependent synthesis of cAMP and activation of PKA and VASP signaling as well as IP-3 dependent Ca2+ release. Hsp90 is highly expressed on the cell surface of melanoma cells, and synthetic agents that target Hsp90 are promising cancer therapeutic drugs. Based on their remarkable antitumor effects, the CDR-H3-derived peptides from RebMab200, and particularly the highly soluble and stable Rb9, are novel candidates to be further studied as potential antitumor drugs, selectively acting on cancer cell motility and invasion. (C) 2016 Elsevier Inc. All rights reserved.
URI: https://repositorio.unifesp.br/handle/11600/56853
ISSN: 0196-9781
Other Identifiers: http://dx.doi.org/10.1016/j.peptides.2016.08.006
Appears in Collections:Artigo
Artigo
Artigo

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.