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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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Detalles Bibliográficos
Autores principales: Crowder, Robert J, Ellis, Matthew J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2005
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.
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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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