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The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy
BACKGROUND: This study aimed to preliminarily assess the relationship between erythropoietin‐producing hepatocellular carcinoma receptor A3 (EphA3) and androgen receptor (AR) protein expression levels and prognosis in prostate cancer (PCa) to better understand the role of EphA3 in the prognosis and...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595293/ https://www.ncbi.nlm.nih.gov/pubmed/30958616 http://dx.doi.org/10.1002/jcla.22871 |
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author | Duan, Xiuzhi Xu, Xiaoming Yin, Binbin Hong, Bong Liu, Weiwei Liu, Qian Tao, Zhihua |
author_facet | Duan, Xiuzhi Xu, Xiaoming Yin, Binbin Hong, Bong Liu, Weiwei Liu, Qian Tao, Zhihua |
author_sort | Duan, Xiuzhi |
collection | PubMed |
description | BACKGROUND: This study aimed to preliminarily assess the relationship between erythropoietin‐producing hepatocellular carcinoma receptor A3 (EphA3) and androgen receptor (AR) protein expression levels and prognosis in prostate cancer (PCa) to better understand the role of EphA3 in the prognosis and progression of PCa. MATERIALS: We investigated the expression of EphA3 and AR in human PCa by immunohistochemistry. RESULTS: EphA3 and AR were both significantly upregulated in PCa, with expression mainly localized to the nucleus. A high level of AR expression was found in 48.4% of 64 tumor samples, which was significantly more than in the adjacent tissue samples (15.6%) (P < 0.01). The percentage of samples expressing a high level of EphA3 was significantly greater in the PCa samples (54.7%) than in the adjacent tissue samples (20.3%) for the 64 tumors (P < 0.01). The high levels of EphA3 and AR expression in the PCa tissue samples were both correlated with the pathological stage, bladder and rectal invasion, distant metastasis, and preoperative PSA level (both P < 0.05). The survival time was significantly shorter in high levels of AR expression of patients. (P < 0.01). A high level of EphA3 in PCa patients suggests a poor prognosis (P < 0.05). Biochemical recurrence, distant metastasis, and the final scores of EphA3 and AR expression were significantly correlated with the prognosis of PCa (P < 0.05). CONCLUSIONS: Increased EphA3 expression is an independent prognostic factor for a poor outcome and decreased survival in PCa. |
format | Online Article Text |
id | pubmed-6595293 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-65952932019-11-12 The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy Duan, Xiuzhi Xu, Xiaoming Yin, Binbin Hong, Bong Liu, Weiwei Liu, Qian Tao, Zhihua J Clin Lab Anal Research Articles BACKGROUND: This study aimed to preliminarily assess the relationship between erythropoietin‐producing hepatocellular carcinoma receptor A3 (EphA3) and androgen receptor (AR) protein expression levels and prognosis in prostate cancer (PCa) to better understand the role of EphA3 in the prognosis and progression of PCa. MATERIALS: We investigated the expression of EphA3 and AR in human PCa by immunohistochemistry. RESULTS: EphA3 and AR were both significantly upregulated in PCa, with expression mainly localized to the nucleus. A high level of AR expression was found in 48.4% of 64 tumor samples, which was significantly more than in the adjacent tissue samples (15.6%) (P < 0.01). The percentage of samples expressing a high level of EphA3 was significantly greater in the PCa samples (54.7%) than in the adjacent tissue samples (20.3%) for the 64 tumors (P < 0.01). The high levels of EphA3 and AR expression in the PCa tissue samples were both correlated with the pathological stage, bladder and rectal invasion, distant metastasis, and preoperative PSA level (both P < 0.05). The survival time was significantly shorter in high levels of AR expression of patients. (P < 0.01). A high level of EphA3 in PCa patients suggests a poor prognosis (P < 0.05). Biochemical recurrence, distant metastasis, and the final scores of EphA3 and AR expression were significantly correlated with the prognosis of PCa (P < 0.05). CONCLUSIONS: Increased EphA3 expression is an independent prognostic factor for a poor outcome and decreased survival in PCa. John Wiley and Sons Inc. 2019-04-08 /pmc/articles/PMC6595293/ /pubmed/30958616 http://dx.doi.org/10.1002/jcla.22871 Text en © 2019 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals, Inc. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Articles Duan, Xiuzhi Xu, Xiaoming Yin, Binbin Hong, Bong Liu, Weiwei Liu, Qian Tao, Zhihua The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
title | The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
title_full | The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
title_fullStr | The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
title_full_unstemmed | The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
title_short | The prognosis value of EphA3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
title_sort | prognosis value of epha3 and the androgen receptor in prostate cancer treated with radical prostatectomy |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6595293/ https://www.ncbi.nlm.nih.gov/pubmed/30958616 http://dx.doi.org/10.1002/jcla.22871 |
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