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Targeting PI3K in cancer: mechanisms and advances in clinical trials

Phosphatidylinositol-3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) signaling is one of the most important intracellular pathways, which can be considered as a master regulator for cancer. Enormous efforts have been dedicated to the development of drugs targeting PI3K signaling, many of wh...

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Detalles Bibliográficos
Autores principales: Yang, Jing, Nie, Ji, Ma, Xuelei, Wei, Yuquan, Peng, Yong, Wei, Xiawei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379961/
https://www.ncbi.nlm.nih.gov/pubmed/30782187
http://dx.doi.org/10.1186/s12943-019-0954-x
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author Yang, Jing
Nie, Ji
Ma, Xuelei
Wei, Yuquan
Peng, Yong
Wei, Xiawei
author_facet Yang, Jing
Nie, Ji
Ma, Xuelei
Wei, Yuquan
Peng, Yong
Wei, Xiawei
author_sort Yang, Jing
collection PubMed
description Phosphatidylinositol-3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) signaling is one of the most important intracellular pathways, which can be considered as a master regulator for cancer. Enormous efforts have been dedicated to the development of drugs targeting PI3K signaling, many of which are currently employed in clinical trials evaluation, and it is becoming increasingly clear that PI3K inhibitors are effective in inhibiting tumor progression. PI3K inhibitors are subdivided into dual PI3K/mTOR inhibitors, pan-PI3K inhibitors and isoform-specific inhibitors. In this review, we performed a critical review to summarize the role of the PI3K pathway in tumor development, recent PI3K inhibitors development based on clinical trials, and the mechanisms of resistance to PI3K inhibition.
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spelling pubmed-63799612019-02-28 Targeting PI3K in cancer: mechanisms and advances in clinical trials Yang, Jing Nie, Ji Ma, Xuelei Wei, Yuquan Peng, Yong Wei, Xiawei Mol Cancer Review Phosphatidylinositol-3-kinase (PI3K)/AKT/mammalian target of rapamycin (mTOR) signaling is one of the most important intracellular pathways, which can be considered as a master regulator for cancer. Enormous efforts have been dedicated to the development of drugs targeting PI3K signaling, many of which are currently employed in clinical trials evaluation, and it is becoming increasingly clear that PI3K inhibitors are effective in inhibiting tumor progression. PI3K inhibitors are subdivided into dual PI3K/mTOR inhibitors, pan-PI3K inhibitors and isoform-specific inhibitors. In this review, we performed a critical review to summarize the role of the PI3K pathway in tumor development, recent PI3K inhibitors development based on clinical trials, and the mechanisms of resistance to PI3K inhibition. BioMed Central 2019-02-19 /pmc/articles/PMC6379961/ /pubmed/30782187 http://dx.doi.org/10.1186/s12943-019-0954-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.
spellingShingle Review
Yang, Jing
Nie, Ji
Ma, Xuelei
Wei, Yuquan
Peng, Yong
Wei, Xiawei
Targeting PI3K in cancer: mechanisms and advances in clinical trials
title Targeting PI3K in cancer: mechanisms and advances in clinical trials
title_full Targeting PI3K in cancer: mechanisms and advances in clinical trials
title_fullStr Targeting PI3K in cancer: mechanisms and advances in clinical trials
title_full_unstemmed Targeting PI3K in cancer: mechanisms and advances in clinical trials
title_short Targeting PI3K in cancer: mechanisms and advances in clinical trials
title_sort targeting pi3k in cancer: mechanisms and advances in clinical trials
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6379961/
https://www.ncbi.nlm.nih.gov/pubmed/30782187
http://dx.doi.org/10.1186/s12943-019-0954-x
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