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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

AC-1001 H3 CDR peptide induces apoptosis and signs of autophagy in vitro and exhibits antimetastatic activity in a syngeneic melanoma model

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Rabaca, Aline N. ; Arruda, Denise C. ; Figueiredo, Carlos R. ; Massaoka, Mariana H. ; Farias, Camyla F. ; Tada, Dayane B. ; Maia, Vera C. ; Silva Junior, Pedro I. ; Girola, Natalia ; Real, Fernando ; Mortara, Renato A. ; Polonelli, Luciano ; Travassos, Luiz R.
Total Authors: 13
Document type: Journal article
Source: FEBS OPEN BIO; v. 6, n. 9, p. 885-901, SEP 2016.
Web of Science Citations: 4
Abstract

Antibody-derived peptides modulate functions of the immune system and are a source of anti-infective and antitumor substances. Recent studies have shown that they comprise amino acid sequences of immunoglobulin complementarity-determining regions, but also fragments of constant regions. V-H CDR3 of murine mAb AC-1001 displays antimetastatic activities using B16F10-Nex2 murine melanoma cells in a syngeneic model. The peptide was cytotoxic in vitro in murine and human melanoma cells inducing reactive oxygen species (ROS) and apoptosis by the intrinsic pathway. Signs of autophagy were also suggested by the increased expression of LC3/LC3II and Beclin 1 and by ultrastructural evidence. AC-1001 H3 bound to both G- and F-actin and inhibited tumor cell migration. These results are important evidence of the antitumor activity of Ig CDR-derived peptides. (AU)

FAPESP's process: 10/16447-6 - Peptides with anti-tumor activity against murine melanoma (B16F10-Nex2.1) and human melanoma(A2058) based on the structure of CDRs (VH1, 2 and 3, VL1, 2 and 3) from mAb AC-1001 and mechanisms of cell death
Grantee:Aline Nogueira Rabaça
Support Opportunities: Scholarships in Brazil - Scientific Initiation