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The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death
Piwi proteins and their interaction with piRNAs have rapidly emerged as important contributors to gene regulation, indicating their crucial function in germline and stem cell development. However, data on the Hiwi 1 (Hiwi) gene, one of the four human Piwi homologues, are still scarce. Therefore, we...
Autores principales: | , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567072/ https://www.ncbi.nlm.nih.gov/pubmed/18781170 http://dx.doi.org/10.1038/sj.bjc.6604653 |
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author | Grochola, L F Greither, T Taubert, H Möller, P Knippschild, U Udelnow, A Henne-Bruns, D Würl, P |
author_facet | Grochola, L F Greither, T Taubert, H Möller, P Knippschild, U Udelnow, A Henne-Bruns, D Würl, P |
author_sort | Grochola, L F |
collection | PubMed |
description | Piwi proteins and their interaction with piRNAs have rapidly emerged as important contributors to gene regulation, indicating their crucial function in germline and stem cell development. However, data on the Hiwi 1 (Hiwi) gene, one of the four human Piwi homologues, are still scarce. Therefore, we investigated the Hiwi mRNA expression in microdissected PDAC tissues from patients with ductal adenocarcinoma of the pancreas (PDAC) by quantitative real-time PCR and the protein expression by immunohistochemistry. Elevated levels of Hiwi mRNA transcripts were measured in 40 out of 56 tissues and a positive immunostaining of Hiwi was detected in tumours of 21 out of 78 patients. There was no general impact of elevated Hiwi mRNA transcript levels or protein expression on survival, as tested by multivariate Cox regression and Kaplan–Meier analysis. However, men showed a significantly increased risk for tumour-related death in case of down- or upregulated expression of Hiwi mRNA (relative risk (RR)=2.78; P=0.034). In summary, we report the first analysis of Hiwi expression in PDAC and its impact on prognosis. We suggest that alterations in mRNA expression of Hiwi can increase the risk of tumour-related death in male PDAC patients. |
format | Text |
id | pubmed-2567072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-25670722009-10-07 The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death Grochola, L F Greither, T Taubert, H Möller, P Knippschild, U Udelnow, A Henne-Bruns, D Würl, P Br J Cancer Molecular Diagnostics Piwi proteins and their interaction with piRNAs have rapidly emerged as important contributors to gene regulation, indicating their crucial function in germline and stem cell development. However, data on the Hiwi 1 (Hiwi) gene, one of the four human Piwi homologues, are still scarce. Therefore, we investigated the Hiwi mRNA expression in microdissected PDAC tissues from patients with ductal adenocarcinoma of the pancreas (PDAC) by quantitative real-time PCR and the protein expression by immunohistochemistry. Elevated levels of Hiwi mRNA transcripts were measured in 40 out of 56 tissues and a positive immunostaining of Hiwi was detected in tumours of 21 out of 78 patients. There was no general impact of elevated Hiwi mRNA transcript levels or protein expression on survival, as tested by multivariate Cox regression and Kaplan–Meier analysis. However, men showed a significantly increased risk for tumour-related death in case of down- or upregulated expression of Hiwi mRNA (relative risk (RR)=2.78; P=0.034). In summary, we report the first analysis of Hiwi expression in PDAC and its impact on prognosis. We suggest that alterations in mRNA expression of Hiwi can increase the risk of tumour-related death in male PDAC patients. Nature Publishing Group 2008-10-07 2008-09-09 /pmc/articles/PMC2567072/ /pubmed/18781170 http://dx.doi.org/10.1038/sj.bjc.6604653 Text en Copyright © 2008 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Molecular Diagnostics Grochola, L F Greither, T Taubert, H Möller, P Knippschild, U Udelnow, A Henne-Bruns, D Würl, P The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
title | The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
title_full | The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
title_fullStr | The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
title_full_unstemmed | The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
title_short | The stem cell-associated Hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
title_sort | stem cell-associated hiwi gene in human adenocarcinoma of the pancreas: expression and risk of tumour-related death |
topic | Molecular Diagnostics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2567072/ https://www.ncbi.nlm.nih.gov/pubmed/18781170 http://dx.doi.org/10.1038/sj.bjc.6604653 |
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