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HER3 in cancer: from the bench to the bedside
The HER3 protein, that belongs to the ErbB/HER receptor tyrosine kinase (RTK) family, is expressed in several types of tumors. That fact, together with the role of HER3 in promoting cell proliferation, implicate that targeting HER3 may have therapeutic relevance. Furthermore, expression and activati...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585794/ https://www.ncbi.nlm.nih.gov/pubmed/36271429 http://dx.doi.org/10.1186/s13046-022-02515-x |
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author | Gandullo-Sánchez, Lucía Ocaña, Alberto Pandiella, Atanasio |
author_facet | Gandullo-Sánchez, Lucía Ocaña, Alberto Pandiella, Atanasio |
author_sort | Gandullo-Sánchez, Lucía |
collection | PubMed |
description | The HER3 protein, that belongs to the ErbB/HER receptor tyrosine kinase (RTK) family, is expressed in several types of tumors. That fact, together with the role of HER3 in promoting cell proliferation, implicate that targeting HER3 may have therapeutic relevance. Furthermore, expression and activation of HER3 has been linked to resistance to drugs that target other HER receptors such as agents that act on EGFR or HER2. In addition, HER3 has been associated to resistance to some chemotherapeutic drugs. Because of those circumstances, efforts to develop and test agents targeting HER3 have been carried out. Two types of agents targeting HER3 have been developed. The most abundant are antibodies or engineered antibody derivatives that specifically recognize the extracellular region of HER3. In addition, the use of aptamers specifically interacting with HER3, vaccines or HER3-targeting siRNAs have also been developed. Here we discuss the state of the art of the preclinical and clinical development of drugs aimed at targeting HER3 with therapeutic purposes. |
format | Online Article Text |
id | pubmed-9585794 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-95857942022-10-22 HER3 in cancer: from the bench to the bedside Gandullo-Sánchez, Lucía Ocaña, Alberto Pandiella, Atanasio J Exp Clin Cancer Res Review The HER3 protein, that belongs to the ErbB/HER receptor tyrosine kinase (RTK) family, is expressed in several types of tumors. That fact, together with the role of HER3 in promoting cell proliferation, implicate that targeting HER3 may have therapeutic relevance. Furthermore, expression and activation of HER3 has been linked to resistance to drugs that target other HER receptors such as agents that act on EGFR or HER2. In addition, HER3 has been associated to resistance to some chemotherapeutic drugs. Because of those circumstances, efforts to develop and test agents targeting HER3 have been carried out. Two types of agents targeting HER3 have been developed. The most abundant are antibodies or engineered antibody derivatives that specifically recognize the extracellular region of HER3. In addition, the use of aptamers specifically interacting with HER3, vaccines or HER3-targeting siRNAs have also been developed. Here we discuss the state of the art of the preclinical and clinical development of drugs aimed at targeting HER3 with therapeutic purposes. BioMed Central 2022-10-21 /pmc/articles/PMC9585794/ /pubmed/36271429 http://dx.doi.org/10.1186/s13046-022-02515-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Gandullo-Sánchez, Lucía Ocaña, Alberto Pandiella, Atanasio HER3 in cancer: from the bench to the bedside |
title | HER3 in cancer: from the bench to the bedside |
title_full | HER3 in cancer: from the bench to the bedside |
title_fullStr | HER3 in cancer: from the bench to the bedside |
title_full_unstemmed | HER3 in cancer: from the bench to the bedside |
title_short | HER3 in cancer: from the bench to the bedside |
title_sort | her3 in cancer: from the bench to the bedside |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9585794/ https://www.ncbi.nlm.nih.gov/pubmed/36271429 http://dx.doi.org/10.1186/s13046-022-02515-x |
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