Cargando…

PGRMC1: a new biomarker for the estrogen receptor in breast cancer

Estrogen receptor (ER) status is a critical biomarker in breast cancer, in large part because the ER is the target of tamoxifen and similar drugs. In the previous issue of Breast Cancer Research, Neubauer and colleagues used a proteomic approach to identify proteins that are differentially regulated...

Descripción completa

Detalles Bibliográficos
Autor principal: Craven, Rolf J
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656908/
https://www.ncbi.nlm.nih.gov/pubmed/19090968
http://dx.doi.org/10.1186/bcr2191
_version_ 1782165542804652032
author Craven, Rolf J
author_facet Craven, Rolf J
author_sort Craven, Rolf J
collection PubMed
description Estrogen receptor (ER) status is a critical biomarker in breast cancer, in large part because the ER is the target of tamoxifen and similar drugs. In the previous issue of Breast Cancer Research, Neubauer and colleagues used a proteomic approach to identify proteins that are differentially regulated by ER in breast tumors. The authors showed that ER-negative tumors have elevated levels of PGRMC1 (progesterone receptor membrane component-1), a hormone receptor component and binding partner for P450 proteins. In contrast, PGRMC1 was phosphorylated in ER-positive tumors. The staining patterns of ER and PGRMC1 were mutually exclusive in breast tumor sections, and PGRMC1 staining was sharply increased in hypoxic areas of the tumor. The results suggest that PGRMC1 is a candidate biomarker for ER status and hypoxia in breast cancer.
format Text
id pubmed-2656908
institution National Center for Biotechnology Information
language English
publishDate 2008
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-26569082009-03-17 PGRMC1: a new biomarker for the estrogen receptor in breast cancer Craven, Rolf J Breast Cancer Res Editorial Estrogen receptor (ER) status is a critical biomarker in breast cancer, in large part because the ER is the target of tamoxifen and similar drugs. In the previous issue of Breast Cancer Research, Neubauer and colleagues used a proteomic approach to identify proteins that are differentially regulated by ER in breast tumors. The authors showed that ER-negative tumors have elevated levels of PGRMC1 (progesterone receptor membrane component-1), a hormone receptor component and binding partner for P450 proteins. In contrast, PGRMC1 was phosphorylated in ER-positive tumors. The staining patterns of ER and PGRMC1 were mutually exclusive in breast tumor sections, and PGRMC1 staining was sharply increased in hypoxic areas of the tumor. The results suggest that PGRMC1 is a candidate biomarker for ER status and hypoxia in breast cancer. BioMed Central 2008 2008-11-24 /pmc/articles/PMC2656908/ /pubmed/19090968 http://dx.doi.org/10.1186/bcr2191 Text en Copyright © 2008 BioMed Central Ltd
spellingShingle Editorial
Craven, Rolf J
PGRMC1: a new biomarker for the estrogen receptor in breast cancer
title PGRMC1: a new biomarker for the estrogen receptor in breast cancer
title_full PGRMC1: a new biomarker for the estrogen receptor in breast cancer
title_fullStr PGRMC1: a new biomarker for the estrogen receptor in breast cancer
title_full_unstemmed PGRMC1: a new biomarker for the estrogen receptor in breast cancer
title_short PGRMC1: a new biomarker for the estrogen receptor in breast cancer
title_sort pgrmc1: a new biomarker for the estrogen receptor in breast cancer
topic Editorial
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2656908/
https://www.ncbi.nlm.nih.gov/pubmed/19090968
http://dx.doi.org/10.1186/bcr2191
work_keys_str_mv AT cravenrolfj pgrmc1anewbiomarkerfortheestrogenreceptorinbreastcancer