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Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis

BACKGROUND: To define the NF-kappaB activation in early stages of hepatocarcinogenesis and its IkappaB's degradation profiles in comparison to sole liver regeneration. METHODS: Western-blot and EMSA analyses were performed for the NF-kappaB activation. The transcriptional activity of NF-kappaB...

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Autores principales: García-Román, Rebeca, Pérez-Carreón, Julio Isael, Márquez-Quiñones, Adriana, Salcido-Neyoy, Martha Estela, Villa-Treviño, Saúl
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1865534/
https://www.ncbi.nlm.nih.gov/pubmed/17445259
http://dx.doi.org/10.1186/1477-3163-6-5
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author García-Román, Rebeca
Pérez-Carreón, Julio Isael
Márquez-Quiñones, Adriana
Salcido-Neyoy, Martha Estela
Villa-Treviño, Saúl
author_facet García-Román, Rebeca
Pérez-Carreón, Julio Isael
Márquez-Quiñones, Adriana
Salcido-Neyoy, Martha Estela
Villa-Treviño, Saúl
author_sort García-Román, Rebeca
collection PubMed
description BACKGROUND: To define the NF-kappaB activation in early stages of hepatocarcinogenesis and its IkappaB's degradation profiles in comparison to sole liver regeneration. METHODS: Western-blot and EMSA analyses were performed for the NF-kappaB activation. The transcriptional activity of NF-kappaB was determined by RT-PCR of the IkappaB-α mRNA. The IkappaB's degradation proteins were determined by Western-blot assay. RESULTS: We demonstrated the persistent activation of NF-kappaB during early stages of hepatocarcinogenesis, which reached maximal level 30 min after partial hepatectomy. The DNA binding and transcriptional activity of NF-kappaB, were sustained during early steps of hepatocarcinogenesis in comparison to only partial hepatectomy, which displayed a transitory NF-kappaB activation. In early stages of hepatocarconogenesis, the IkappaB-α degradation turned out to be acute and transitory, but the low levels of IkappaB-β persisted even 15 days after partial hepatectomy. Interestingly, IkappaB-β degradation is not induced after sole partial hepatectomy. CONCLUSION: We propose that during liver regeneration, the transitory stimulation of the transcription factor response, assures blockade of NF-kappaB until recovery of the total mass of the liver and the persistent NF-kappaB activation in early hepatocarcinogenesis may be due to IkappaB-β and IkappaB-α degradation, mainly IkappaB-β degradation, which contributes to gene transcription related to proliferation required for neoplasic progression.
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spelling pubmed-18655342007-05-05 Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis García-Román, Rebeca Pérez-Carreón, Julio Isael Márquez-Quiñones, Adriana Salcido-Neyoy, Martha Estela Villa-Treviño, Saúl J Carcinog Research BACKGROUND: To define the NF-kappaB activation in early stages of hepatocarcinogenesis and its IkappaB's degradation profiles in comparison to sole liver regeneration. METHODS: Western-blot and EMSA analyses were performed for the NF-kappaB activation. The transcriptional activity of NF-kappaB was determined by RT-PCR of the IkappaB-α mRNA. The IkappaB's degradation proteins were determined by Western-blot assay. RESULTS: We demonstrated the persistent activation of NF-kappaB during early stages of hepatocarcinogenesis, which reached maximal level 30 min after partial hepatectomy. The DNA binding and transcriptional activity of NF-kappaB, were sustained during early steps of hepatocarcinogenesis in comparison to only partial hepatectomy, which displayed a transitory NF-kappaB activation. In early stages of hepatocarconogenesis, the IkappaB-α degradation turned out to be acute and transitory, but the low levels of IkappaB-β persisted even 15 days after partial hepatectomy. Interestingly, IkappaB-β degradation is not induced after sole partial hepatectomy. CONCLUSION: We propose that during liver regeneration, the transitory stimulation of the transcription factor response, assures blockade of NF-kappaB until recovery of the total mass of the liver and the persistent NF-kappaB activation in early hepatocarcinogenesis may be due to IkappaB-β and IkappaB-α degradation, mainly IkappaB-β degradation, which contributes to gene transcription related to proliferation required for neoplasic progression. BioMed Central 2007-04-19 /pmc/articles/PMC1865534/ /pubmed/17445259 http://dx.doi.org/10.1186/1477-3163-6-5 Text en Copyright © 2007 García-Román et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
García-Román, Rebeca
Pérez-Carreón, Julio Isael
Márquez-Quiñones, Adriana
Salcido-Neyoy, Martha Estela
Villa-Treviño, Saúl
Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis
title Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis
title_full Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis
title_fullStr Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis
title_full_unstemmed Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis
title_short Persistent activation of NF-kappaB related to IkappaB's degradation profiles during early chemical hepatocarcinogenesis
title_sort persistent activation of nf-kappab related to ikappab's degradation profiles during early chemical hepatocarcinogenesis
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1865534/
https://www.ncbi.nlm.nih.gov/pubmed/17445259
http://dx.doi.org/10.1186/1477-3163-6-5
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