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The Potential of panHER Inhibition in Cancer

Purpose: Hyper-activation of the HER (erbB) family receptors, HER 1-4, leads to up-regulation of the three vital signaling pathways: mitogen activated protein kinase, phosphoinositide 3-kinase/AKT, and Janus kinase/signal transducer and activator of transcription pathways. Blocking HER1/EGFR has a l...

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Autores principales: Wang, Xiaochun, Batty, Kathleen M., Crowe, Philip J., Goldstein, David, Yang, Jia-Lin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309158/
https://www.ncbi.nlm.nih.gov/pubmed/25674538
http://dx.doi.org/10.3389/fonc.2015.00002
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author Wang, Xiaochun
Batty, Kathleen M.
Crowe, Philip J.
Goldstein, David
Yang, Jia-Lin
author_facet Wang, Xiaochun
Batty, Kathleen M.
Crowe, Philip J.
Goldstein, David
Yang, Jia-Lin
author_sort Wang, Xiaochun
collection PubMed
description Purpose: Hyper-activation of the HER (erbB) family receptors, HER 1-4, leads to up-regulation of the three vital signaling pathways: mitogen activated protein kinase, phosphoinositide 3-kinase/AKT, and Janus kinase/signal transducer and activator of transcription pathways. Blocking HER1/EGFR has a limited anticancer effect due to either secondary mutation e.g., T790M or by-pass signaling of other HER members. The emergence of an anti-panHER approach to blockade of these pathways as a cancer treatment may provide a solution to this resistance. This review aimed to provide an overview of the HER signaling pathways and their involvement in tumor progression and examine the current progress in panHER inhibition. Methods: Recent literature associated with HER signaling pathways and panHER inhibition was reviewed through PubMed and Medline database, followed by critical comparison and analysis. Results: Pre-clinical studies and clinical trials of panHER inhibitors show promising results, and the potential to improve patient outcomes in solid cancers. Conclusion: The use of panHER inhibitors in cancers with HER-family hyper-activation, such as other epithelial cancers and sarcoma, is a new direction to research and has potential in clinical cancer therapy in the future.
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spelling pubmed-43091582015-02-11 The Potential of panHER Inhibition in Cancer Wang, Xiaochun Batty, Kathleen M. Crowe, Philip J. Goldstein, David Yang, Jia-Lin Front Oncol Oncology Purpose: Hyper-activation of the HER (erbB) family receptors, HER 1-4, leads to up-regulation of the three vital signaling pathways: mitogen activated protein kinase, phosphoinositide 3-kinase/AKT, and Janus kinase/signal transducer and activator of transcription pathways. Blocking HER1/EGFR has a limited anticancer effect due to either secondary mutation e.g., T790M or by-pass signaling of other HER members. The emergence of an anti-panHER approach to blockade of these pathways as a cancer treatment may provide a solution to this resistance. This review aimed to provide an overview of the HER signaling pathways and their involvement in tumor progression and examine the current progress in panHER inhibition. Methods: Recent literature associated with HER signaling pathways and panHER inhibition was reviewed through PubMed and Medline database, followed by critical comparison and analysis. Results: Pre-clinical studies and clinical trials of panHER inhibitors show promising results, and the potential to improve patient outcomes in solid cancers. Conclusion: The use of panHER inhibitors in cancers with HER-family hyper-activation, such as other epithelial cancers and sarcoma, is a new direction to research and has potential in clinical cancer therapy in the future. Frontiers Media S.A. 2015-01-28 /pmc/articles/PMC4309158/ /pubmed/25674538 http://dx.doi.org/10.3389/fonc.2015.00002 Text en Copyright © 2015 Wang, Batty, Crowe, Goldstein and Yang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wang, Xiaochun
Batty, Kathleen M.
Crowe, Philip J.
Goldstein, David
Yang, Jia-Lin
The Potential of panHER Inhibition in Cancer
title The Potential of panHER Inhibition in Cancer
title_full The Potential of panHER Inhibition in Cancer
title_fullStr The Potential of panHER Inhibition in Cancer
title_full_unstemmed The Potential of panHER Inhibition in Cancer
title_short The Potential of panHER Inhibition in Cancer
title_sort potential of panher inhibition in cancer
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309158/
https://www.ncbi.nlm.nih.gov/pubmed/25674538
http://dx.doi.org/10.3389/fonc.2015.00002
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