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Hlavní autor: Mamoor, Shahan
Médium: Recurso digital
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Vydáno: Zenodo 2025
On-line přístup:https://doi.org/10.5281/zenodo.16640207
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author Mamoor, Shahan
author_facet Mamoor, Shahan
contents <p dir="ltr">Breast cancer can be positive for expression of a hormone receptor (ESR/PGR/AR) or a growth factor receptor (ERBB2).  Disease recurrence following disease remission (relapse), resistance to endocrine therapy or otherwise inadequate long-term control of disease are challenges that limit effectiveness of existing drugs that treat luminal A and luminal B disease.  Here we utilized whole transcriptome technologies (5, 6) to measure total transcription in the primary tumors of humans with luminal A and luminal B breast cancer.  We describe one member of a group of phosphatases up-regulated and differentially expressed in human luminal B breast cancer, PGP, as a catalytically available phosphatase and candidate therapeutic target for the adjunctive medical treatment of luminal B breast cancer.    </p>
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spellingShingle Phosphatase targeting in Luminal B breast cancer: PGP.
Mamoor, Shahan
<p dir="ltr">Breast cancer can be positive for expression of a hormone receptor (ESR/PGR/AR) or a growth factor receptor (ERBB2).  Disease recurrence following disease remission (relapse), resistance to endocrine therapy or otherwise inadequate long-term control of disease are challenges that limit effectiveness of existing drugs that treat luminal A and luminal B disease.  Here we utilized whole transcriptome technologies (5, 6) to measure total transcription in the primary tumors of humans with luminal A and luminal B breast cancer.  We describe one member of a group of phosphatases up-regulated and differentially expressed in human luminal B breast cancer, PGP, as a catalytically available phosphatase and candidate therapeutic target for the adjunctive medical treatment of luminal B breast cancer.    </p>
title Phosphatase targeting in Luminal B breast cancer: PGP.
url https://doi.org/10.5281/zenodo.16640207