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Splice Variants of Androgen Receptor and Prostate Cancer
Over the last ten years, two new-generation hormonal drugs and two chemotherapeutic agents have been approved for the treatment of metastatic castration-resistant prostate cancer. Unfortunately, some patients have primary resistance to them and the others eventually develop secondary resistance. It...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PAGEPress Publications, Pavia, Italy
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943095/ https://www.ncbi.nlm.nih.gov/pubmed/27471583 http://dx.doi.org/10.4081/oncol.2016.297 |
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author | Caffo, Orazio Maines, Francesca Veccia, Antonello Kinspergher, Stefania Galligioni, Enzo |
author_facet | Caffo, Orazio Maines, Francesca Veccia, Antonello Kinspergher, Stefania Galligioni, Enzo |
author_sort | Caffo, Orazio |
collection | PubMed |
description | Over the last ten years, two new-generation hormonal drugs and two chemotherapeutic agents have been approved for the treatment of metastatic castration-resistant prostate cancer. Unfortunately, some patients have primary resistance to them and the others eventually develop secondary resistance. It has recently been suggested that the presence of androgen receptor splice variants plays a leading role in the primary and secondary resistance to the new hormonal drugs, whereas their presence seem to have only a partial effect on the activity of the chemotherapeutic agents. The aim of this paper is to review the published data concerning the role of androgen receptor splice variants in prostate cancer biology, and their potential use as biomarkers when making therapeutic decisions. |
format | Online Article Text |
id | pubmed-4943095 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | PAGEPress Publications, Pavia, Italy |
record_format | MEDLINE/PubMed |
spelling | pubmed-49430952016-07-28 Splice Variants of Androgen Receptor and Prostate Cancer Caffo, Orazio Maines, Francesca Veccia, Antonello Kinspergher, Stefania Galligioni, Enzo Oncol Rev Review Over the last ten years, two new-generation hormonal drugs and two chemotherapeutic agents have been approved for the treatment of metastatic castration-resistant prostate cancer. Unfortunately, some patients have primary resistance to them and the others eventually develop secondary resistance. It has recently been suggested that the presence of androgen receptor splice variants plays a leading role in the primary and secondary resistance to the new hormonal drugs, whereas their presence seem to have only a partial effect on the activity of the chemotherapeutic agents. The aim of this paper is to review the published data concerning the role of androgen receptor splice variants in prostate cancer biology, and their potential use as biomarkers when making therapeutic decisions. PAGEPress Publications, Pavia, Italy 2016-05-30 /pmc/articles/PMC4943095/ /pubmed/27471583 http://dx.doi.org/10.4081/oncol.2016.297 Text en ©Copyright O. Caffo et al. http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License (by-nc 3.0) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Review Caffo, Orazio Maines, Francesca Veccia, Antonello Kinspergher, Stefania Galligioni, Enzo Splice Variants of Androgen Receptor and Prostate Cancer |
title | Splice Variants of Androgen Receptor and Prostate Cancer |
title_full | Splice Variants of Androgen Receptor and Prostate Cancer |
title_fullStr | Splice Variants of Androgen Receptor and Prostate Cancer |
title_full_unstemmed | Splice Variants of Androgen Receptor and Prostate Cancer |
title_short | Splice Variants of Androgen Receptor and Prostate Cancer |
title_sort | splice variants of androgen receptor and prostate cancer |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4943095/ https://www.ncbi.nlm.nih.gov/pubmed/27471583 http://dx.doi.org/10.4081/oncol.2016.297 |
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