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Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer

Loss of erythropoietin-producing hepatocyte (Eph) B6 gene expression is associated with poor prognosis in neuroblastoma, melanoma and other tumors. The present study evaluated the expression of EphB6 receptor tyrosine kinase in normal and prostate cancer tissue using immunohistochemistry. The associ...

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Autores principales: MOHAMED, ELNISR RASHED, NOGUCHI, MASANORI, HAMED, AHMED ROSHDI, ELDAHSHOURY, MOHAMED ZAKI, HAMMADY, AHMED RASHED, SALEM, ESAM ELDEN, ITOH, KYOGO
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356330/
https://www.ncbi.nlm.nih.gov/pubmed/25789021
http://dx.doi.org/10.3892/ol.2015.2925
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author MOHAMED, ELNISR RASHED
NOGUCHI, MASANORI
HAMED, AHMED ROSHDI
ELDAHSHOURY, MOHAMED ZAKI
HAMMADY, AHMED RASHED
SALEM, ESAM ELDEN
ITOH, KYOGO
author_facet MOHAMED, ELNISR RASHED
NOGUCHI, MASANORI
HAMED, AHMED ROSHDI
ELDAHSHOURY, MOHAMED ZAKI
HAMMADY, AHMED RASHED
SALEM, ESAM ELDEN
ITOH, KYOGO
author_sort MOHAMED, ELNISR RASHED
collection PubMed
description Loss of erythropoietin-producing hepatocyte (Eph) B6 gene expression is associated with poor prognosis in neuroblastoma, melanoma and other tumors. The present study evaluated the expression of EphB6 receptor tyrosine kinase in normal and prostate cancer tissue using immunohistochemistry. The association between EphB6 expression, clinicopathological findings, proliferating-cell nuclear antigen (PCNA; another prognostic marker) and progression of prostate cancer was analyzed. Tissue microarray samples of normal prostatic tissue and prostate cancer tissue from 46 patients treated with radical prostatectomy for prostate cancer were included in this study. Polyclonal anti-EphB6 and monoclonal anti-PCNA antibodies were used to assess EphB6 and PCNA expression by immunohistochemistry. EphB6 was expressed in normal and prostate cancer tissue; however, its expression was significantly reduced in prostate cancer tissue compared with normal prostatic tissue (P<0.0001), in high volume (≥4 cm(3)) cancer compared with low volume (<4 cm(3); P=0.015), and in pT3 stage compared with pT2 stage of the disease (P=0.0007). No correlation was observed between the expression of EphB6 and PCNA. Short biochemical progression-free survival was associated with low EphB6 protein expression (P=0.157). This study revealed that EphB6 may have a tumor suppressor effect in prostate cancer, at least during early stages of this disease. This provides new insight into the potential utility of EphB6 receptor as a diagnostic/prognostic marker for prostate cancer.
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spelling pubmed-43563302015-03-18 Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer MOHAMED, ELNISR RASHED NOGUCHI, MASANORI HAMED, AHMED ROSHDI ELDAHSHOURY, MOHAMED ZAKI HAMMADY, AHMED RASHED SALEM, ESAM ELDEN ITOH, KYOGO Oncol Lett Articles Loss of erythropoietin-producing hepatocyte (Eph) B6 gene expression is associated with poor prognosis in neuroblastoma, melanoma and other tumors. The present study evaluated the expression of EphB6 receptor tyrosine kinase in normal and prostate cancer tissue using immunohistochemistry. The association between EphB6 expression, clinicopathological findings, proliferating-cell nuclear antigen (PCNA; another prognostic marker) and progression of prostate cancer was analyzed. Tissue microarray samples of normal prostatic tissue and prostate cancer tissue from 46 patients treated with radical prostatectomy for prostate cancer were included in this study. Polyclonal anti-EphB6 and monoclonal anti-PCNA antibodies were used to assess EphB6 and PCNA expression by immunohistochemistry. EphB6 was expressed in normal and prostate cancer tissue; however, its expression was significantly reduced in prostate cancer tissue compared with normal prostatic tissue (P<0.0001), in high volume (≥4 cm(3)) cancer compared with low volume (<4 cm(3); P=0.015), and in pT3 stage compared with pT2 stage of the disease (P=0.0007). No correlation was observed between the expression of EphB6 and PCNA. Short biochemical progression-free survival was associated with low EphB6 protein expression (P=0.157). This study revealed that EphB6 may have a tumor suppressor effect in prostate cancer, at least during early stages of this disease. This provides new insight into the potential utility of EphB6 receptor as a diagnostic/prognostic marker for prostate cancer. D.A. Spandidos 2015-04 2015-02-03 /pmc/articles/PMC4356330/ /pubmed/25789021 http://dx.doi.org/10.3892/ol.2015.2925 Text en Copyright © 2015, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
MOHAMED, ELNISR RASHED
NOGUCHI, MASANORI
HAMED, AHMED ROSHDI
ELDAHSHOURY, MOHAMED ZAKI
HAMMADY, AHMED RASHED
SALEM, ESAM ELDEN
ITOH, KYOGO
Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer
title Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer
title_full Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer
title_fullStr Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer
title_full_unstemmed Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer
title_short Reduced expression of erythropoietin-producing hepatocyte B6 receptor tyrosine kinase in prostate cancer
title_sort reduced expression of erythropoietin-producing hepatocyte b6 receptor tyrosine kinase in prostate cancer
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4356330/
https://www.ncbi.nlm.nih.gov/pubmed/25789021
http://dx.doi.org/10.3892/ol.2015.2925
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