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Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway
Recent studies indicate that constitutive signaling through the phosphatidylinositol 3'-kinase (PI3K) pathway is a cause of treatment resistance in breast cancer patients. This implies that patients with tumors that exhibit aberrant PI3K signaling may benefit from targeted pathway inhibitors. T...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2005
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1242159/ https://www.ncbi.nlm.nih.gov/pubmed/16168140 http://dx.doi.org/10.1186/bcr1307 |
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author | Crowder, Robert J Ellis, Matthew J |
author_facet | Crowder, Robert J Ellis, Matthew J |
author_sort | Crowder, Robert J |
collection | PubMed |
description | Recent studies indicate that constitutive signaling through the phosphatidylinositol 3'-kinase (PI3K) pathway is a cause of treatment resistance in breast cancer patients. This implies that patients with tumors that exhibit aberrant PI3K signaling may benefit from targeted pathway inhibitors. The first agents to make it to the clinic are the rapamycin analogs. These compounds inhibit the downstream PI3K effector mTOR (mammalian target of rapamycin). A study presented in this issue of Breast Cancer Research suggests that recently developed inhibitors of phosphoinositide-dependent protein kinase 1, a more proximal target of the PI3K pathway, may provide an alternative route to effective PI3K pathway inhibition for breast cancer treatment. |
format | Text |
id | pubmed-1242159 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2005 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-12421592005-10-06 Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway Crowder, Robert J Ellis, Matthew J Breast Cancer Res Commentary Recent studies indicate that constitutive signaling through the phosphatidylinositol 3'-kinase (PI3K) pathway is a cause of treatment resistance in breast cancer patients. This implies that patients with tumors that exhibit aberrant PI3K signaling may benefit from targeted pathway inhibitors. The first agents to make it to the clinic are the rapamycin analogs. These compounds inhibit the downstream PI3K effector mTOR (mammalian target of rapamycin). A study presented in this issue of Breast Cancer Research suggests that recently developed inhibitors of phosphoinositide-dependent protein kinase 1, a more proximal target of the PI3K pathway, may provide an alternative route to effective PI3K pathway inhibition for breast cancer treatment. BioMed Central 2005 2005-08-05 /pmc/articles/PMC1242159/ /pubmed/16168140 http://dx.doi.org/10.1186/bcr1307 Text en Copyright © 2005 BioMed Central Ltd |
spellingShingle | Commentary Crowder, Robert J Ellis, Matthew J Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
title | Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
title_full | Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
title_fullStr | Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
title_full_unstemmed | Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
title_short | Treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
title_sort | treating breast cancer through novel inhibitors of the phosphatidylinositol 3'-kinase pathway |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1242159/ https://www.ncbi.nlm.nih.gov/pubmed/16168140 http://dx.doi.org/10.1186/bcr1307 |
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