5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores.
The contribution of 5α-reductase 1 and 5α-reductase 2 to prostate cancer development and progression is not clearly understood. TRAMP mice are a common prostate cancer model, in which 5α-reductase 1 and 5α-reductase 2 expression levels, along with prostate lesions scores, have not been investigated...
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doaj-8a9adad6192d4afdaa250951107d24f82020-11-25T00:04:43ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-01125e017587410.1371/journal.pone.01758745α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores.Alexander B Opoku-AcheampongJamie N HenningsonAmanda P BeckBrian L LindshieldThe contribution of 5α-reductase 1 and 5α-reductase 2 to prostate cancer development and progression is not clearly understood. TRAMP mice are a common prostate cancer model, in which 5α-reductase 1 and 5α-reductase 2 expression levels, along with prostate lesions scores, have not been investigated at different time points to further understand prostate carcinogenesis.To this end, 8-, 12-, 16-, and 20-week-old male C57BL/6TRAMP x FVB mice prostate most severe and most common lesion scores, 5α-reductase 1 and 5α-reductase 2 in situ hybridization expression, and Ki-67, androgen receptor, and apoptosis immunohistochemistry levels were measured. Levels of these markers were quantified in prostate epithelium, hyperplasia, and tumors sections. Mice developed low- to high-grade prostatic intraepithelial neoplasia at 8 weeks as the most severe and most common lesions, and moderate- and high-grade prostatic intraepithelial neoplasia at 12 and 16 weeks as the most severe lesion in all lobes. Moderately differentiated adenocarcinoma was observed at 20 weeks in all lobes. Poorly differentiated carcinoma was not observed in any lobe until 12-weeks-old. 5α-reductase 1 and 5α-reductase 2 were not significantly decreased in tumors compared to prostate epithelium and hyperplasia in all groups, while proliferation, apoptosis, and androgen receptor were either notably or significantly decreased in tumors compared with prostate epithelium and hyperplasia in most or all groups. Prostate 5αR1 levels were positively correlated with adjusted prostate most severe lesion scores.Downregulation of androgen receptor and 5α-reductase 2, along with upregulation of 5α-reductase 1 in tumors may promote prostatic intraepithelial neoplasia and prostate cancer development in TRAMP mice.http://europepmc.org/articles/PMC5426600?pdf=render |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alexander B Opoku-Acheampong Jamie N Henningson Amanda P Beck Brian L Lindshield |
spellingShingle |
Alexander B Opoku-Acheampong Jamie N Henningson Amanda P Beck Brian L Lindshield 5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores. PLoS ONE |
author_facet |
Alexander B Opoku-Acheampong Jamie N Henningson Amanda P Beck Brian L Lindshield |
author_sort |
Alexander B Opoku-Acheampong |
title |
5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores. |
title_short |
5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores. |
title_full |
5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores. |
title_fullStr |
5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores. |
title_full_unstemmed |
5α-reductase 1 mRNA levels are positively correlated with TRAMP mouse prostate most severe lesion scores. |
title_sort |
5α-reductase 1 mrna levels are positively correlated with tramp mouse prostate most severe lesion scores. |
publisher |
Public Library of Science (PLoS) |
series |
PLoS ONE |
issn |
1932-6203 |
publishDate |
2017-01-01 |
description |
The contribution of 5α-reductase 1 and 5α-reductase 2 to prostate cancer development and progression is not clearly understood. TRAMP mice are a common prostate cancer model, in which 5α-reductase 1 and 5α-reductase 2 expression levels, along with prostate lesions scores, have not been investigated at different time points to further understand prostate carcinogenesis.To this end, 8-, 12-, 16-, and 20-week-old male C57BL/6TRAMP x FVB mice prostate most severe and most common lesion scores, 5α-reductase 1 and 5α-reductase 2 in situ hybridization expression, and Ki-67, androgen receptor, and apoptosis immunohistochemistry levels were measured. Levels of these markers were quantified in prostate epithelium, hyperplasia, and tumors sections. Mice developed low- to high-grade prostatic intraepithelial neoplasia at 8 weeks as the most severe and most common lesions, and moderate- and high-grade prostatic intraepithelial neoplasia at 12 and 16 weeks as the most severe lesion in all lobes. Moderately differentiated adenocarcinoma was observed at 20 weeks in all lobes. Poorly differentiated carcinoma was not observed in any lobe until 12-weeks-old. 5α-reductase 1 and 5α-reductase 2 were not significantly decreased in tumors compared to prostate epithelium and hyperplasia in all groups, while proliferation, apoptosis, and androgen receptor were either notably or significantly decreased in tumors compared with prostate epithelium and hyperplasia in most or all groups. Prostate 5αR1 levels were positively correlated with adjusted prostate most severe lesion scores.Downregulation of androgen receptor and 5α-reductase 2, along with upregulation of 5α-reductase 1 in tumors may promote prostatic intraepithelial neoplasia and prostate cancer development in TRAMP mice. |
url |
http://europepmc.org/articles/PMC5426600?pdf=render |
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