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Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma
OBJECTIVE: To investigate the expression of androgen receptor (AR) and its correlation with disease status and survival outcome in uterine leiomyosarcoma with other hormone receptors. METHODS: The medical records and paraffin blocks of 42 patients were reviewed. The immunohistochemical expression of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920217/ https://www.ncbi.nlm.nih.gov/pubmed/29533018 http://dx.doi.org/10.3802/jgo.2018.29.e30 |
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author | Baek, Min-Hyun Park, Jeong-Yeol Park, Yangsoon Kim, Kyu-Rae Kim, Dae-Yeon Suh, Dae-Shik Kim, Jong-Hyeok Kim, Yong-Man Kim, Young-Tak Nam, Joo-Hyun |
author_facet | Baek, Min-Hyun Park, Jeong-Yeol Park, Yangsoon Kim, Kyu-Rae Kim, Dae-Yeon Suh, Dae-Shik Kim, Jong-Hyeok Kim, Yong-Man Kim, Young-Tak Nam, Joo-Hyun |
author_sort | Baek, Min-Hyun |
collection | PubMed |
description | OBJECTIVE: To investigate the expression of androgen receptor (AR) and its correlation with disease status and survival outcome in uterine leiomyosarcoma with other hormone receptors. METHODS: The medical records and paraffin blocks of 42 patients were reviewed. The immunohistochemical expression of AR, estrogen receptor (ER), progesterone receptor (PR), gonadotropin releasing hormone (GnRH), and cytochrome P450, family 19, subfamily A, polypeptide 1 (CYP19A1) were assessed using tissue microarray. RESULTS: In total, AR expression was observed in 11 patients (26.2%). International Federation of Gynecology and Obstetrics (FIGO) stage and AR were independent factors for disease-free survival (DFS) in multivariate regression analysis (odds ratio [OR]=5.8; 95% confidence interval [CI]=1.2–28.4 and OR=0.2; 95% CI=0.05–0.90; p=0.029 and 0.032, respectively). There were no deaths in the AR expression group, whereas the 5-year overall survival (OS) was 54.8% in the no expression group (p=0.014). Co-expression of ER and/or PR with AR was associated with significantly better 5-year DFS and OS than those with negative AR (72.7% vs. 28.6% and 100% vs. 64.3%; p=0.020 and 0.036, respectively). AR may be an independent prognostic marker regardless of ER/PR. CONCLUSION: AR can be a potential prognostic biomarker in uterine leiomyosarcoma. |
format | Online Article Text |
id | pubmed-5920217 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-59202172018-05-01 Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma Baek, Min-Hyun Park, Jeong-Yeol Park, Yangsoon Kim, Kyu-Rae Kim, Dae-Yeon Suh, Dae-Shik Kim, Jong-Hyeok Kim, Yong-Man Kim, Young-Tak Nam, Joo-Hyun J Gynecol Oncol Original Article OBJECTIVE: To investigate the expression of androgen receptor (AR) and its correlation with disease status and survival outcome in uterine leiomyosarcoma with other hormone receptors. METHODS: The medical records and paraffin blocks of 42 patients were reviewed. The immunohistochemical expression of AR, estrogen receptor (ER), progesterone receptor (PR), gonadotropin releasing hormone (GnRH), and cytochrome P450, family 19, subfamily A, polypeptide 1 (CYP19A1) were assessed using tissue microarray. RESULTS: In total, AR expression was observed in 11 patients (26.2%). International Federation of Gynecology and Obstetrics (FIGO) stage and AR were independent factors for disease-free survival (DFS) in multivariate regression analysis (odds ratio [OR]=5.8; 95% confidence interval [CI]=1.2–28.4 and OR=0.2; 95% CI=0.05–0.90; p=0.029 and 0.032, respectively). There were no deaths in the AR expression group, whereas the 5-year overall survival (OS) was 54.8% in the no expression group (p=0.014). Co-expression of ER and/or PR with AR was associated with significantly better 5-year DFS and OS than those with negative AR (72.7% vs. 28.6% and 100% vs. 64.3%; p=0.020 and 0.036, respectively). AR may be an independent prognostic marker regardless of ER/PR. CONCLUSION: AR can be a potential prognostic biomarker in uterine leiomyosarcoma. Asian Society of Gynecologic Oncology; Korean Society of Gynecologic Oncology 2018-05 2018-02-05 /pmc/articles/PMC5920217/ /pubmed/29533018 http://dx.doi.org/10.3802/jgo.2018.29.e30 Text en Copyright © 2018. Asian Society of Gynecologic Oncology, Korean Society of Gynecologic Oncology https://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Baek, Min-Hyun Park, Jeong-Yeol Park, Yangsoon Kim, Kyu-Rae Kim, Dae-Yeon Suh, Dae-Shik Kim, Jong-Hyeok Kim, Yong-Man Kim, Young-Tak Nam, Joo-Hyun Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
title | Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
title_full | Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
title_fullStr | Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
title_full_unstemmed | Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
title_short | Androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
title_sort | androgen receptor as a prognostic biomarker and therapeutic target in uterine leiomyosarcoma |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5920217/ https://www.ncbi.nlm.nih.gov/pubmed/29533018 http://dx.doi.org/10.3802/jgo.2018.29.e30 |
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