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Proteomic Study to Survey the CIGB-552 Antitumor Effect
CIGB-552 is a cell-penetrating peptide that exerts in vitro and in vivo antitumor effect on cancer cells. In the present work, the mechanism involved in such anticancer activity was studied using chemical proteomics and expression-based proteomics in culture cancer cell lines. CIGB-552 interacts wit...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630370/ https://www.ncbi.nlm.nih.gov/pubmed/26576414 http://dx.doi.org/10.1155/2015/124082 |
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author | Rodríguez-Ulloa, Arielis Gil, Jeovanis Ramos, Yassel Hernández-Álvarez, Lilian Flores, Lisandra Oliva, Brizaida García, Dayana Sánchez-Puente, Aniel Musacchio-Lasa, Alexis Fernández-de-Cossio, Jorge Padrón, Gabriel González López, Luis J. Besada, Vladimir Guerra-Vallespí, Maribel |
author_facet | Rodríguez-Ulloa, Arielis Gil, Jeovanis Ramos, Yassel Hernández-Álvarez, Lilian Flores, Lisandra Oliva, Brizaida García, Dayana Sánchez-Puente, Aniel Musacchio-Lasa, Alexis Fernández-de-Cossio, Jorge Padrón, Gabriel González López, Luis J. Besada, Vladimir Guerra-Vallespí, Maribel |
author_sort | Rodríguez-Ulloa, Arielis |
collection | PubMed |
description | CIGB-552 is a cell-penetrating peptide that exerts in vitro and in vivo antitumor effect on cancer cells. In the present work, the mechanism involved in such anticancer activity was studied using chemical proteomics and expression-based proteomics in culture cancer cell lines. CIGB-552 interacts with at least 55 proteins, as determined by chemical proteomics. A temporal differential proteomics based on iTRAQ quantification method was performed to identify CIGB-552 modulated proteins. The proteomic profile includes 72 differentially expressed proteins in response to CIGB-552 treatment. Proteins related to cell proliferation and apoptosis were identified by both approaches. In line with previous findings, proteomic data revealed that CIGB-552 triggers the inhibition of NF-κB signaling pathway. Furthermore, proteins related to cell invasion were differentially modulated by CIGB-552 treatment suggesting new potentialities of CIGB-552 as anticancer agent. Overall, the current study contributes to a better understanding of the antitumor action mechanism of CIGB-552. |
format | Online Article Text |
id | pubmed-4630370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-46303702015-11-16 Proteomic Study to Survey the CIGB-552 Antitumor Effect Rodríguez-Ulloa, Arielis Gil, Jeovanis Ramos, Yassel Hernández-Álvarez, Lilian Flores, Lisandra Oliva, Brizaida García, Dayana Sánchez-Puente, Aniel Musacchio-Lasa, Alexis Fernández-de-Cossio, Jorge Padrón, Gabriel González López, Luis J. Besada, Vladimir Guerra-Vallespí, Maribel Biomed Res Int Research Article CIGB-552 is a cell-penetrating peptide that exerts in vitro and in vivo antitumor effect on cancer cells. In the present work, the mechanism involved in such anticancer activity was studied using chemical proteomics and expression-based proteomics in culture cancer cell lines. CIGB-552 interacts with at least 55 proteins, as determined by chemical proteomics. A temporal differential proteomics based on iTRAQ quantification method was performed to identify CIGB-552 modulated proteins. The proteomic profile includes 72 differentially expressed proteins in response to CIGB-552 treatment. Proteins related to cell proliferation and apoptosis were identified by both approaches. In line with previous findings, proteomic data revealed that CIGB-552 triggers the inhibition of NF-κB signaling pathway. Furthermore, proteins related to cell invasion were differentially modulated by CIGB-552 treatment suggesting new potentialities of CIGB-552 as anticancer agent. Overall, the current study contributes to a better understanding of the antitumor action mechanism of CIGB-552. Hindawi Publishing Corporation 2015 2015-10-20 /pmc/articles/PMC4630370/ /pubmed/26576414 http://dx.doi.org/10.1155/2015/124082 Text en Copyright © 2015 Arielis Rodríguez-Ulloa et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Rodríguez-Ulloa, Arielis Gil, Jeovanis Ramos, Yassel Hernández-Álvarez, Lilian Flores, Lisandra Oliva, Brizaida García, Dayana Sánchez-Puente, Aniel Musacchio-Lasa, Alexis Fernández-de-Cossio, Jorge Padrón, Gabriel González López, Luis J. Besada, Vladimir Guerra-Vallespí, Maribel Proteomic Study to Survey the CIGB-552 Antitumor Effect |
title | Proteomic Study to Survey the CIGB-552 Antitumor Effect |
title_full | Proteomic Study to Survey the CIGB-552 Antitumor Effect |
title_fullStr | Proteomic Study to Survey the CIGB-552 Antitumor Effect |
title_full_unstemmed | Proteomic Study to Survey the CIGB-552 Antitumor Effect |
title_short | Proteomic Study to Survey the CIGB-552 Antitumor Effect |
title_sort | proteomic study to survey the cigb-552 antitumor effect |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4630370/ https://www.ncbi.nlm.nih.gov/pubmed/26576414 http://dx.doi.org/10.1155/2015/124082 |
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