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Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC
In the light of current treatment developments for non-small cell lung cancer (NSCLC), the idea of a plastic cellular tumorigenic network bound by key paracrine signaling pathways mediating resistances to targeted therapies is brought forward. Based on a review of available preclinical and clinical...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522169/ https://www.ncbi.nlm.nih.gov/pubmed/28402937 http://dx.doi.org/10.18632/oncotarget.16674 |
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author | Langhammer, Stefan Scheerer, Joachim |
author_facet | Langhammer, Stefan Scheerer, Joachim |
author_sort | Langhammer, Stefan |
collection | PubMed |
description | In the light of current treatment developments for non-small cell lung cancer (NSCLC), the idea of a plastic cellular tumorigenic network bound by key paracrine signaling pathways mediating resistances to targeted therapies is brought forward. Based on a review of available preclinical and clinical data in NSCLC combinational approaches to address drivers of this network with marketed drugs are discussed. Five criteria for selecting drug combination regimens aiming at its disruption and thereby overcoming resistances are postulated. |
format | Online Article Text |
id | pubmed-5522169 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-55221692017-08-08 Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC Langhammer, Stefan Scheerer, Joachim Oncotarget Review In the light of current treatment developments for non-small cell lung cancer (NSCLC), the idea of a plastic cellular tumorigenic network bound by key paracrine signaling pathways mediating resistances to targeted therapies is brought forward. Based on a review of available preclinical and clinical data in NSCLC combinational approaches to address drivers of this network with marketed drugs are discussed. Five criteria for selecting drug combination regimens aiming at its disruption and thereby overcoming resistances are postulated. Impact Journals LLC 2017-03-29 /pmc/articles/PMC5522169/ /pubmed/28402937 http://dx.doi.org/10.18632/oncotarget.16674 Text en Copyright: © 2017 Langhammer and Scheerer http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Review Langhammer, Stefan Scheerer, Joachim Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC |
title | Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC |
title_full | Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC |
title_fullStr | Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC |
title_full_unstemmed | Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC |
title_short | Breaking the crosstalk of the cellular tumorigenic network: Hypothesis for addressing resistances to targeted therapies in advanced NSCLC |
title_sort | breaking the crosstalk of the cellular tumorigenic network: hypothesis for addressing resistances to targeted therapies in advanced nsclc |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5522169/ https://www.ncbi.nlm.nih.gov/pubmed/28402937 http://dx.doi.org/10.18632/oncotarget.16674 |
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