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Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers
BACKGROUND: Prolyl hydroxylase 1 (PHD1) is a prognostic marker in several cancers. AIMS AND SCOPES: This study was undertaken to elucidate the clinical relevance of PHD1 in colorectal cancer (CRC) prognosis. MATERIALS AND METHODS: We compared PHD1 expression on a tissue microarray (TMA) containing s...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374750/ https://www.ncbi.nlm.nih.gov/pubmed/36976352 http://dx.doi.org/10.1007/s00432-023-04717-y |
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author | Melling, Nathaniel Grass, Julia Reeh, Matthias Tachezy, Michael Blessmann, Marco Nickel, Felix Hackert, Thilo Grupp, Katharina |
author_facet | Melling, Nathaniel Grass, Julia Reeh, Matthias Tachezy, Michael Blessmann, Marco Nickel, Felix Hackert, Thilo Grupp, Katharina |
author_sort | Melling, Nathaniel |
collection | PubMed |
description | BACKGROUND: Prolyl hydroxylase 1 (PHD1) is a prognostic marker in several cancers. AIMS AND SCOPES: This study was undertaken to elucidate the clinical relevance of PHD1 in colorectal cancer (CRC) prognosis. MATERIALS AND METHODS: We compared PHD1 expression on a tissue microarray (TMA) containing samples from 1800 CRCs with corresponding clinicopathological tumor variables and patient survival. RESULTS: While PHD1 staining was always high in benign colorectal epithelium, high PHD1 staining was detectable in only 71.8% of CRCs. Low PHD1 staining was associated with advanced tumor stage (p = 0.0101) and shortened overall survival in CRC patients (p = 0.0011). In a multivariable analysis including tumor stage, histological type and PHD1 staining revealed tumor stage and histological type (p < 0.0001 each), but also PHD1 staining (p = 0.0202) to be independent prognostic markers for CRC. CONCLUSIONS: In our cohort, loss of PHD1 expression independently identified a subset of CRC patients with poor overall survival and might, thus, be a promising prognostic marker. PHD1 targeting may even allow for specific therapeutic approaches for these patients. |
format | Online Article Text |
id | pubmed-10374750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-103747502023-07-29 Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers Melling, Nathaniel Grass, Julia Reeh, Matthias Tachezy, Michael Blessmann, Marco Nickel, Felix Hackert, Thilo Grupp, Katharina J Cancer Res Clin Oncol Research BACKGROUND: Prolyl hydroxylase 1 (PHD1) is a prognostic marker in several cancers. AIMS AND SCOPES: This study was undertaken to elucidate the clinical relevance of PHD1 in colorectal cancer (CRC) prognosis. MATERIALS AND METHODS: We compared PHD1 expression on a tissue microarray (TMA) containing samples from 1800 CRCs with corresponding clinicopathological tumor variables and patient survival. RESULTS: While PHD1 staining was always high in benign colorectal epithelium, high PHD1 staining was detectable in only 71.8% of CRCs. Low PHD1 staining was associated with advanced tumor stage (p = 0.0101) and shortened overall survival in CRC patients (p = 0.0011). In a multivariable analysis including tumor stage, histological type and PHD1 staining revealed tumor stage and histological type (p < 0.0001 each), but also PHD1 staining (p = 0.0202) to be independent prognostic markers for CRC. CONCLUSIONS: In our cohort, loss of PHD1 expression independently identified a subset of CRC patients with poor overall survival and might, thus, be a promising prognostic marker. PHD1 targeting may even allow for specific therapeutic approaches for these patients. Springer Berlin Heidelberg 2023-03-28 2023 /pmc/articles/PMC10374750/ /pubmed/36976352 http://dx.doi.org/10.1007/s00432-023-04717-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Research Melling, Nathaniel Grass, Julia Reeh, Matthias Tachezy, Michael Blessmann, Marco Nickel, Felix Hackert, Thilo Grupp, Katharina Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
title | Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
title_full | Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
title_fullStr | Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
title_full_unstemmed | Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
title_short | Decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
title_sort | decreased expression of prolyl hydroxylase 1 is associated with poor prognosis in colorectal cancers |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10374750/ https://www.ncbi.nlm.nih.gov/pubmed/36976352 http://dx.doi.org/10.1007/s00432-023-04717-y |
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