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Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK)
Phosphoinositide 3-kinases (PI3K) and phosphoinositide 3-kinase-related protein kinases (PIKK) are two structurally related families of kinases that play vital roles in cell growth and DNA damage repair. Dysfunction of PIKK members and aberrant stimulation of the PI3K/AKT/mTOR signalling pathway are...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392309/ https://www.ncbi.nlm.nih.gov/pubmed/37489050 http://dx.doi.org/10.1080/14756366.2023.2237209 |
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author | Huang, Xueqin You, Li Nepovimova, Eugenie Psotka, Miroslav Malinak, David Valko, Marian Sivak, Ladislav Korabecny, Jan Heger, Zbynek Adam, Vojtech Wu, Qinghua Kuca, Kamil |
author_facet | Huang, Xueqin You, Li Nepovimova, Eugenie Psotka, Miroslav Malinak, David Valko, Marian Sivak, Ladislav Korabecny, Jan Heger, Zbynek Adam, Vojtech Wu, Qinghua Kuca, Kamil |
author_sort | Huang, Xueqin |
collection | PubMed |
description | Phosphoinositide 3-kinases (PI3K) and phosphoinositide 3-kinase-related protein kinases (PIKK) are two structurally related families of kinases that play vital roles in cell growth and DNA damage repair. Dysfunction of PIKK members and aberrant stimulation of the PI3K/AKT/mTOR signalling pathway are linked to a plethora of diseases including cancer. In recent decades, numerous inhibitors related to the PI3K/AKT/mTOR signalling have made great strides in cancer treatment, like copanlisib and sirolimus. Notably, most of the PIKK inhibitors (such as VX-970 and M3814) related to DNA damage response have also shown good efficacy in clinical trials. However, these drugs still require a suitable combination therapy to overcome drug resistance or improve antitumor activity. Based on the aforementioned facts, we summarised the efficacy of PIKK, PI3K, and AKT inhibitors in the therapy of human malignancies and the resistance mechanisms of targeted therapy, in order to provide deeper insights into cancer treatment. |
format | Online Article Text |
id | pubmed-10392309 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-103923092023-08-02 Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) Huang, Xueqin You, Li Nepovimova, Eugenie Psotka, Miroslav Malinak, David Valko, Marian Sivak, Ladislav Korabecny, Jan Heger, Zbynek Adam, Vojtech Wu, Qinghua Kuca, Kamil J Enzyme Inhib Med Chem Review Article Phosphoinositide 3-kinases (PI3K) and phosphoinositide 3-kinase-related protein kinases (PIKK) are two structurally related families of kinases that play vital roles in cell growth and DNA damage repair. Dysfunction of PIKK members and aberrant stimulation of the PI3K/AKT/mTOR signalling pathway are linked to a plethora of diseases including cancer. In recent decades, numerous inhibitors related to the PI3K/AKT/mTOR signalling have made great strides in cancer treatment, like copanlisib and sirolimus. Notably, most of the PIKK inhibitors (such as VX-970 and M3814) related to DNA damage response have also shown good efficacy in clinical trials. However, these drugs still require a suitable combination therapy to overcome drug resistance or improve antitumor activity. Based on the aforementioned facts, we summarised the efficacy of PIKK, PI3K, and AKT inhibitors in the therapy of human malignancies and the resistance mechanisms of targeted therapy, in order to provide deeper insights into cancer treatment. Taylor & Francis 2023-07-24 /pmc/articles/PMC10392309/ /pubmed/37489050 http://dx.doi.org/10.1080/14756366.2023.2237209 Text en © 2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. The terms on which this article has been published allow the posting of the Accepted Manuscript in a repository by the author(s) or with their consent. |
spellingShingle | Review Article Huang, Xueqin You, Li Nepovimova, Eugenie Psotka, Miroslav Malinak, David Valko, Marian Sivak, Ladislav Korabecny, Jan Heger, Zbynek Adam, Vojtech Wu, Qinghua Kuca, Kamil Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) |
title | Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) |
title_full | Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) |
title_fullStr | Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) |
title_full_unstemmed | Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) |
title_short | Inhibitors of phosphoinositide 3-kinase (PI3K) and phosphoinositide 3-kinase-related protein kinase family (PIKK) |
title_sort | inhibitors of phosphoinositide 3-kinase (pi3k) and phosphoinositide 3-kinase-related protein kinase family (pikk) |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10392309/ https://www.ncbi.nlm.nih.gov/pubmed/37489050 http://dx.doi.org/10.1080/14756366.2023.2237209 |
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