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PTEN Inhibition in Human Disease Therapy
The tumor suppressor PTEN is a major homeostatic regulator, by virtue of its lipid phosphatase activity against phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P3], which downregulates the PI3K/AKT/mTOR prosurvival signaling, as well as by its protein phosphatase activity towards specific protein...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2018
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017825/ https://www.ncbi.nlm.nih.gov/pubmed/29385737 http://dx.doi.org/10.3390/molecules23020285 |
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author | Pulido, Rafael |
author_facet | Pulido, Rafael |
author_sort | Pulido, Rafael |
collection | PubMed |
description | The tumor suppressor PTEN is a major homeostatic regulator, by virtue of its lipid phosphatase activity against phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P3], which downregulates the PI3K/AKT/mTOR prosurvival signaling, as well as by its protein phosphatase activity towards specific protein targets. PTEN catalytic activity is crucial to control cell growth under physiologic and pathologic situations, and it impacts not only in preventing tumor cell survival and proliferation, but also in restraining several cellular regeneration processes, such as those associated with nerve injury recovery, cardiac ischemia, or wound healing. In these conditions, inhibition of PTEN catalysis is being explored as a potentially beneficial therapeutic intervention. Here, an overview of human diseases and conditions in which PTEN inhibition could be beneficial is presented, together with an update on the current status of specific small molecule inhibitors of PTEN enzymatic activity, their use in experimental models, and their limitations as research or therapeutic drugs. |
format | Online Article Text |
id | pubmed-6017825 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-60178252018-11-13 PTEN Inhibition in Human Disease Therapy Pulido, Rafael Molecules Review The tumor suppressor PTEN is a major homeostatic regulator, by virtue of its lipid phosphatase activity against phosphatidylinositol 3,4,5-trisphosphate [PI(3,4,5)P3], which downregulates the PI3K/AKT/mTOR prosurvival signaling, as well as by its protein phosphatase activity towards specific protein targets. PTEN catalytic activity is crucial to control cell growth under physiologic and pathologic situations, and it impacts not only in preventing tumor cell survival and proliferation, but also in restraining several cellular regeneration processes, such as those associated with nerve injury recovery, cardiac ischemia, or wound healing. In these conditions, inhibition of PTEN catalysis is being explored as a potentially beneficial therapeutic intervention. Here, an overview of human diseases and conditions in which PTEN inhibition could be beneficial is presented, together with an update on the current status of specific small molecule inhibitors of PTEN enzymatic activity, their use in experimental models, and their limitations as research or therapeutic drugs. MDPI 2018-01-30 /pmc/articles/PMC6017825/ /pubmed/29385737 http://dx.doi.org/10.3390/molecules23020285 Text en © 2018 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Pulido, Rafael PTEN Inhibition in Human Disease Therapy |
title | PTEN Inhibition in Human Disease Therapy |
title_full | PTEN Inhibition in Human Disease Therapy |
title_fullStr | PTEN Inhibition in Human Disease Therapy |
title_full_unstemmed | PTEN Inhibition in Human Disease Therapy |
title_short | PTEN Inhibition in Human Disease Therapy |
title_sort | pten inhibition in human disease therapy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6017825/ https://www.ncbi.nlm.nih.gov/pubmed/29385737 http://dx.doi.org/10.3390/molecules23020285 |
work_keys_str_mv | AT pulidorafael pteninhibitioninhumandiseasetherapy |