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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
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.
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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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