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Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs
Platinum drugs continue to be major chemotherapy drugs for cancer treatment. Nevertheless, acquired or intrinsic resistance to these compounds is common in human tumors. One important mechanism for this resistance is the avoidance of cells entering the apoptotic pathway. Nuclear factor-kappa B (NF-k...
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Formato: | Texto |
Lenguaje: | English |
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Hindawi Publishing Corporation
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291150/ https://www.ncbi.nlm.nih.gov/pubmed/18414584 http://dx.doi.org/10.1155/2008/576104 |
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author | Lagunas, Vilma Maldonado Meléndez-Zajgla, Jorge |
author_facet | Lagunas, Vilma Maldonado Meléndez-Zajgla, Jorge |
author_sort | Lagunas, Vilma Maldonado |
collection | PubMed |
description | Platinum drugs continue to be major chemotherapy drugs for cancer treatment. Nevertheless, acquired or intrinsic resistance to these compounds is common in human tumors. One important mechanism for this resistance is the avoidance of cells entering the apoptotic pathway. Nuclear factor-kappa B (NF-kappa B, NF-κB) is a pleiotropic transcription factor key in determining the death threshold of human cells. This factor is important in the final response of cells to platinum drugs, as exemplified by in vitro and in vivo models showing that inhibition of NF-κB sensitizes cancer cells to the effects of these drugs. New approaches focusing on the inhibition of NF-κB could help to minimize or even eliminate intrinsic or acquired resistance to platinum drugs. |
format | Text |
id | pubmed-2291150 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-22911502008-04-14 Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs Lagunas, Vilma Maldonado Meléndez-Zajgla, Jorge Met Based Drugs Review Article Platinum drugs continue to be major chemotherapy drugs for cancer treatment. Nevertheless, acquired or intrinsic resistance to these compounds is common in human tumors. One important mechanism for this resistance is the avoidance of cells entering the apoptotic pathway. Nuclear factor-kappa B (NF-kappa B, NF-κB) is a pleiotropic transcription factor key in determining the death threshold of human cells. This factor is important in the final response of cells to platinum drugs, as exemplified by in vitro and in vivo models showing that inhibition of NF-κB sensitizes cancer cells to the effects of these drugs. New approaches focusing on the inhibition of NF-κB could help to minimize or even eliminate intrinsic or acquired resistance to platinum drugs. Hindawi Publishing Corporation 2008 2008-04-08 /pmc/articles/PMC2291150/ /pubmed/18414584 http://dx.doi.org/10.1155/2008/576104 Text en Copyright © 2008 V. M. Lagunas and J. Meléndez-Zajgla. 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 | Review Article Lagunas, Vilma Maldonado Meléndez-Zajgla, Jorge Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs |
title | Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs |
title_full | Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs |
title_fullStr | Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs |
title_full_unstemmed | Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs |
title_short | Nuclear Factor-kappa B as a Resistance Factor to Platinum-Based Antineoplasic Drugs |
title_sort | nuclear factor-kappa b as a resistance factor to platinum-based antineoplasic drugs |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2291150/ https://www.ncbi.nlm.nih.gov/pubmed/18414584 http://dx.doi.org/10.1155/2008/576104 |
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