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Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer

There is emerging evidence asserting the importance of orphan nuclear receptors (ONRs) in cancer initiation and progression. In breast cancer, there is a lot unknown about ONRs in terms of their expression profile and their transcriptional targets in the various stages of tumor progression. With the...

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Autores principales: Aesoy, Reidun, Clyne, Colin D., Chand, Ashwini L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528200/
https://www.ncbi.nlm.nih.gov/pubmed/26300846
http://dx.doi.org/10.3389/fendo.2015.00115
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author Aesoy, Reidun
Clyne, Colin D.
Chand, Ashwini L.
author_facet Aesoy, Reidun
Clyne, Colin D.
Chand, Ashwini L.
author_sort Aesoy, Reidun
collection PubMed
description There is emerging evidence asserting the importance of orphan nuclear receptors (ONRs) in cancer initiation and progression. In breast cancer, there is a lot unknown about ONRs in terms of their expression profile and their transcriptional targets in the various stages of tumor progression. With the classification of breast tumors into distinct molecular subtypes, we assess ONR expression in the different breast cancer subtypes and with patient outcomes. Complementing this, we review evidence implicating ONR-dependent molecular pathways in breast cancer progression to identify candidate ONRs as potential prognostic markers and/or as therapeutic targets.
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spelling pubmed-45282002015-08-21 Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer Aesoy, Reidun Clyne, Colin D. Chand, Ashwini L. Front Endocrinol (Lausanne) Endocrinology There is emerging evidence asserting the importance of orphan nuclear receptors (ONRs) in cancer initiation and progression. In breast cancer, there is a lot unknown about ONRs in terms of their expression profile and their transcriptional targets in the various stages of tumor progression. With the classification of breast tumors into distinct molecular subtypes, we assess ONR expression in the different breast cancer subtypes and with patient outcomes. Complementing this, we review evidence implicating ONR-dependent molecular pathways in breast cancer progression to identify candidate ONRs as potential prognostic markers and/or as therapeutic targets. Frontiers Media S.A. 2015-08-07 /pmc/articles/PMC4528200/ /pubmed/26300846 http://dx.doi.org/10.3389/fendo.2015.00115 Text en Copyright © 2015 Aesoy, Clyne and Chand. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Aesoy, Reidun
Clyne, Colin D.
Chand, Ashwini L.
Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer
title Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer
title_full Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer
title_fullStr Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer
title_full_unstemmed Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer
title_short Insights into Orphan Nuclear Receptors as Prognostic Markers and Novel Therapeutic Targets for Breast Cancer
title_sort insights into orphan nuclear receptors as prognostic markers and novel therapeutic targets for breast cancer
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4528200/
https://www.ncbi.nlm.nih.gov/pubmed/26300846
http://dx.doi.org/10.3389/fendo.2015.00115
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