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Targeting ERK-Hippo Interplay in Cancer Therapy

Extracellular signal-regulated kinase (ERK) is a part of the mitogen-activated protein kinase (MAPK) signaling pathway which allows the transduction of various cellular signals to final effectors and regulation of elementary cellular processes. Deregulation of the MAPK signaling occurs under many pa...

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Detalles Bibliográficos
Autores principales: Vališ, Karel, Novák, Petr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247570/
https://www.ncbi.nlm.nih.gov/pubmed/32375238
http://dx.doi.org/10.3390/ijms21093236
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author Vališ, Karel
Novák, Petr
author_facet Vališ, Karel
Novák, Petr
author_sort Vališ, Karel
collection PubMed
description Extracellular signal-regulated kinase (ERK) is a part of the mitogen-activated protein kinase (MAPK) signaling pathway which allows the transduction of various cellular signals to final effectors and regulation of elementary cellular processes. Deregulation of the MAPK signaling occurs under many pathological conditions including neurodegenerative disorders, metabolic syndromes and cancers. Targeted inhibition of individual kinases of the MAPK signaling pathway using synthetic compounds represents a promising way to effective anti-cancer therapy. Cross-talk of the MAPK signaling pathway with other proteins and signaling pathways have a crucial impact on clinical outcomes of targeted therapies and plays important role during development of drug resistance in cancers. We discuss cross-talk of the MAPK/ERK signaling pathway with other signaling pathways, in particular interplay with the Hippo/MST pathway. We demonstrate the mechanism of cell death induction shared between MAPK/ERK and Hippo/MST signaling pathways and discuss the potential of combination targeting of these pathways in the development of more effective anti-cancer therapies.
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spelling pubmed-72475702020-06-10 Targeting ERK-Hippo Interplay in Cancer Therapy Vališ, Karel Novák, Petr Int J Mol Sci Review Extracellular signal-regulated kinase (ERK) is a part of the mitogen-activated protein kinase (MAPK) signaling pathway which allows the transduction of various cellular signals to final effectors and regulation of elementary cellular processes. Deregulation of the MAPK signaling occurs under many pathological conditions including neurodegenerative disorders, metabolic syndromes and cancers. Targeted inhibition of individual kinases of the MAPK signaling pathway using synthetic compounds represents a promising way to effective anti-cancer therapy. Cross-talk of the MAPK signaling pathway with other proteins and signaling pathways have a crucial impact on clinical outcomes of targeted therapies and plays important role during development of drug resistance in cancers. We discuss cross-talk of the MAPK/ERK signaling pathway with other signaling pathways, in particular interplay with the Hippo/MST pathway. We demonstrate the mechanism of cell death induction shared between MAPK/ERK and Hippo/MST signaling pathways and discuss the potential of combination targeting of these pathways in the development of more effective anti-cancer therapies. MDPI 2020-05-03 /pmc/articles/PMC7247570/ /pubmed/32375238 http://dx.doi.org/10.3390/ijms21093236 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Vališ, Karel
Novák, Petr
Targeting ERK-Hippo Interplay in Cancer Therapy
title Targeting ERK-Hippo Interplay in Cancer Therapy
title_full Targeting ERK-Hippo Interplay in Cancer Therapy
title_fullStr Targeting ERK-Hippo Interplay in Cancer Therapy
title_full_unstemmed Targeting ERK-Hippo Interplay in Cancer Therapy
title_short Targeting ERK-Hippo Interplay in Cancer Therapy
title_sort targeting erk-hippo interplay in cancer therapy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247570/
https://www.ncbi.nlm.nih.gov/pubmed/32375238
http://dx.doi.org/10.3390/ijms21093236
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