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Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control

Modified nucleosides, regarded as indicators for the whole-body turnover of RNAs, are excreted in abnormal amounts in the urine of patients with malignancies. To test their usefulness as tumour markers and to compare them with the conventional tumour markers, fractionated urine samples were analysed...

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Autores principales: Seidel, A, Brunner, S, Seidel, P, Fritz, G I, Herbarth, O
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361309/
https://www.ncbi.nlm.nih.gov/pubmed/16685264
http://dx.doi.org/10.1038/sj.bjc.6603164
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author Seidel, A
Brunner, S
Seidel, P
Fritz, G I
Herbarth, O
author_facet Seidel, A
Brunner, S
Seidel, P
Fritz, G I
Herbarth, O
author_sort Seidel, A
collection PubMed
description Modified nucleosides, regarded as indicators for the whole-body turnover of RNAs, are excreted in abnormal amounts in the urine of patients with malignancies. To test their usefulness as tumour markers and to compare them with the conventional tumour markers, fractionated urine samples were analysed using chromatography. The excretion patterns of nucleosides of 68 cancer patients with malignant and benign tumours and 41 healthy controls have been studied. Significant elevations in the total sum and the concentrations of at least three (or four) of indicator nucleosides cytidine, pseudouridine, 2-pyridone-5-carboxamide-N1-ribofuranoside, N2,N2-dimethylguanine, 1-methylguanosine, 2-methylguanosine and 1-methyladenosine indicate a tumour with a sensitivity of 54% (77%) and a specificity of 86% (98%). Using an artificial neural network analysis, a sensitivity of 97% and a specificity of 85% were achieved in differentiating between tumour and control volunteers. The comparison with carcinoembryonic antigen, cancer antigen 15-3 und tissue polypeptide antigen indicates that urinary nucleosides may be useful tumour markers. This study suggests that the simultaneous determination of modified nucleosides and creatinine in urine samples of patients with cancer leads to an advantage to current methods and is a useful method to detect cancer early and to control the success of therapy.
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spelling pubmed-23613092009-09-10 Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control Seidel, A Brunner, S Seidel, P Fritz, G I Herbarth, O Br J Cancer Molecular Diagnostics Modified nucleosides, regarded as indicators for the whole-body turnover of RNAs, are excreted in abnormal amounts in the urine of patients with malignancies. To test their usefulness as tumour markers and to compare them with the conventional tumour markers, fractionated urine samples were analysed using chromatography. The excretion patterns of nucleosides of 68 cancer patients with malignant and benign tumours and 41 healthy controls have been studied. Significant elevations in the total sum and the concentrations of at least three (or four) of indicator nucleosides cytidine, pseudouridine, 2-pyridone-5-carboxamide-N1-ribofuranoside, N2,N2-dimethylguanine, 1-methylguanosine, 2-methylguanosine and 1-methyladenosine indicate a tumour with a sensitivity of 54% (77%) and a specificity of 86% (98%). Using an artificial neural network analysis, a sensitivity of 97% and a specificity of 85% were achieved in differentiating between tumour and control volunteers. The comparison with carcinoembryonic antigen, cancer antigen 15-3 und tissue polypeptide antigen indicates that urinary nucleosides may be useful tumour markers. This study suggests that the simultaneous determination of modified nucleosides and creatinine in urine samples of patients with cancer leads to an advantage to current methods and is a useful method to detect cancer early and to control the success of therapy. Nature Publishing Group 2006-06-05 2006-05-09 /pmc/articles/PMC2361309/ /pubmed/16685264 http://dx.doi.org/10.1038/sj.bjc.6603164 Text en Copyright © 2006 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
Seidel, A
Brunner, S
Seidel, P
Fritz, G I
Herbarth, O
Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
title Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
title_full Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
title_fullStr Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
title_full_unstemmed Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
title_short Modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
title_sort modified nucleosides: an accurate tumour marker for clinical diagnosis of cancer, early detection and therapy control
topic Molecular Diagnostics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2361309/
https://www.ncbi.nlm.nih.gov/pubmed/16685264
http://dx.doi.org/10.1038/sj.bjc.6603164
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