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HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD)
INTRODUCTION: Bladder cancer (BC) is a serious medical problem. The high rate of recurrence and progression demands the development of new methods, such as genetic markers, which allow diagnosis and patient follow-up. OBJECTIVES: The aim of this study was to compare expression of HIF-1, GLUT1, endog...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Polish Urological Association
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921788/ https://www.ncbi.nlm.nih.gov/pubmed/24578952 http://dx.doi.org/10.5173/ceju.2012.03.art10 |
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author | Markowski, Michał Lipiński, Marek Krzeslak, Anna Forma, Ewa Bryś, Magdalena Różański, Waldemar |
author_facet | Markowski, Michał Lipiński, Marek Krzeslak, Anna Forma, Ewa Bryś, Magdalena Różański, Waldemar |
author_sort | Markowski, Michał |
collection | PubMed |
description | INTRODUCTION: Bladder cancer (BC) is a serious medical problem. The high rate of recurrence and progression demands the development of new methods, such as genetic markers, which allow diagnosis and patient follow-up. OBJECTIVES: The aim of this study was to compare expression of HIF-1, GLUT1, endoglin, and BRIC5 in patients without and those with BC. The second group was divided into sub-groups: those without a history of PDD (photodynamic diagnosis) in the diagnostic process and those after PDD. METHODS: Patients with BC were diagnosed using the PDD method using hexaminolevulinate (Hexvix(®)). The expressions of HIF-1, GLUT1, endoglin, and BRIC5 genes were established in urine specimens by real-time quantitative polymerase chain reaction (PCR). RESULTS: The expressions of all tested genes were higher in the group of patients with BC than in the group without BC. In the group after PDD, a statistically significant overexpression of HIF-1 was observed. In this group, changes were not observed in cases of the other three tested genes. CONCLUSIONS: The differences between the group with PDD and the group without it can be connected with the direct influence of PDD on malignant tissue, which can cause overexpression of HIF-1 only. This is, however, only a hypothesis and needs further study. |
format | Online Article Text |
id | pubmed-3921788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Polish Urological Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-39217882014-02-27 HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) Markowski, Michał Lipiński, Marek Krzeslak, Anna Forma, Ewa Bryś, Magdalena Różański, Waldemar Cent European J Urol Basic Science INTRODUCTION: Bladder cancer (BC) is a serious medical problem. The high rate of recurrence and progression demands the development of new methods, such as genetic markers, which allow diagnosis and patient follow-up. OBJECTIVES: The aim of this study was to compare expression of HIF-1, GLUT1, endoglin, and BRIC5 in patients without and those with BC. The second group was divided into sub-groups: those without a history of PDD (photodynamic diagnosis) in the diagnostic process and those after PDD. METHODS: Patients with BC were diagnosed using the PDD method using hexaminolevulinate (Hexvix(®)). The expressions of HIF-1, GLUT1, endoglin, and BRIC5 genes were established in urine specimens by real-time quantitative polymerase chain reaction (PCR). RESULTS: The expressions of all tested genes were higher in the group of patients with BC than in the group without BC. In the group after PDD, a statistically significant overexpression of HIF-1 was observed. In this group, changes were not observed in cases of the other three tested genes. CONCLUSIONS: The differences between the group with PDD and the group without it can be connected with the direct influence of PDD on malignant tissue, which can cause overexpression of HIF-1 only. This is, however, only a hypothesis and needs further study. Polish Urological Association 2012-09-04 2012 /pmc/articles/PMC3921788/ /pubmed/24578952 http://dx.doi.org/10.5173/ceju.2012.03.art10 Text en Copyright by Polish Urological Association http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Basic Science Markowski, Michał Lipiński, Marek Krzeslak, Anna Forma, Ewa Bryś, Magdalena Różański, Waldemar HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) |
title | HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) |
title_full | HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) |
title_fullStr | HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) |
title_full_unstemmed | HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) |
title_short | HIF-1, GLUT1, endoglin, and BIRC5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (PDD) |
title_sort | hif-1, glut1, endoglin, and birc5 expression in urine samples obtained from patients with bladder malignancies – after photodynamic diagnosis (pdd) |
topic | Basic Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3921788/ https://www.ncbi.nlm.nih.gov/pubmed/24578952 http://dx.doi.org/10.5173/ceju.2012.03.art10 |
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