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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...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2007
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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. |
format | Text |
id | pubmed-1865534 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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