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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...

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Detalles Bibliográficos
Autores principales: Langhammer, Stefan, Scheerer, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
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.
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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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