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Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy
Aurora kinase A (AURKA) belongs to the family of serine/threonine kinases, whose activation is necessary for cell division processes via regulation of mitosis. AURKA shows significantly higher expression in cancer tissues than in normal control tissues for multiple tumor types according to the TCGA...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809767/ https://www.ncbi.nlm.nih.gov/pubmed/33451333 http://dx.doi.org/10.1186/s12943-020-01305-3 |
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author | Du, Ruijuan Huang, Chuntian Liu, Kangdong Li, Xiang Dong, Zigang |
author_facet | Du, Ruijuan Huang, Chuntian Liu, Kangdong Li, Xiang Dong, Zigang |
author_sort | Du, Ruijuan |
collection | PubMed |
description | Aurora kinase A (AURKA) belongs to the family of serine/threonine kinases, whose activation is necessary for cell division processes via regulation of mitosis. AURKA shows significantly higher expression in cancer tissues than in normal control tissues for multiple tumor types according to the TCGA database. Activation of AURKA has been demonstrated to play an important role in a wide range of cancers, and numerous AURKA substrates have been identified. AURKA-mediated phosphorylation can regulate the functions of AURKA substrates, some of which are mitosis regulators, tumor suppressors or oncogenes. In addition, enrichment of AURKA-interacting proteins with KEGG pathway and GO analysis have demonstrated that these proteins are involved in classic oncogenic pathways. All of this evidence favors the idea of AURKA as a target for cancer therapy, and some small molecules targeting AURKA have been discovered. These AURKA inhibitors (AKIs) have been tested in preclinical studies, and some of them have been subjected to clinical trials as monotherapies or in combination with classic chemotherapy or other targeted therapies. |
format | Online Article Text |
id | pubmed-7809767 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-78097672021-01-15 Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy Du, Ruijuan Huang, Chuntian Liu, Kangdong Li, Xiang Dong, Zigang Mol Cancer Review Aurora kinase A (AURKA) belongs to the family of serine/threonine kinases, whose activation is necessary for cell division processes via regulation of mitosis. AURKA shows significantly higher expression in cancer tissues than in normal control tissues for multiple tumor types according to the TCGA database. Activation of AURKA has been demonstrated to play an important role in a wide range of cancers, and numerous AURKA substrates have been identified. AURKA-mediated phosphorylation can regulate the functions of AURKA substrates, some of which are mitosis regulators, tumor suppressors or oncogenes. In addition, enrichment of AURKA-interacting proteins with KEGG pathway and GO analysis have demonstrated that these proteins are involved in classic oncogenic pathways. All of this evidence favors the idea of AURKA as a target for cancer therapy, and some small molecules targeting AURKA have been discovered. These AURKA inhibitors (AKIs) have been tested in preclinical studies, and some of them have been subjected to clinical trials as monotherapies or in combination with classic chemotherapy or other targeted therapies. BioMed Central 2021-01-15 /pmc/articles/PMC7809767/ /pubmed/33451333 http://dx.doi.org/10.1186/s12943-020-01305-3 Text en © The Author(s) 2021 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/. The Creative Commons Public Domain Dedication waiver (http://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 Du, Ruijuan Huang, Chuntian Liu, Kangdong Li, Xiang Dong, Zigang Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy |
title | Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy |
title_full | Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy |
title_fullStr | Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy |
title_full_unstemmed | Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy |
title_short | Targeting AURKA in Cancer: molecular mechanisms and opportunities for Cancer therapy |
title_sort | targeting aurka in cancer: molecular mechanisms and opportunities for cancer therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809767/ https://www.ncbi.nlm.nih.gov/pubmed/33451333 http://dx.doi.org/10.1186/s12943-020-01305-3 |
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