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Modified Nucleosides and Cancer

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Cover of 'Modified Nucleosides and Cancer'

Table of Contents

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    Book Overview
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    Chapter 1 Organization and Expression of tRNA Genes in Drosophila Melanogaster
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    Chapter 2 Chemical Nature, Properties, Location, and Physiological and Pathological Variations of Modified Nucleosides in tRNAs
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    Chapter 3 Formation and Removal of Methylated Nucleosides in Nucleic Acids of Mammalian Cells
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    Chapter 4 Structural Modifications and Repair of DNA in Neuro-Oncogenesis by N-Ethyl-N-nitrosourea
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    Chapter 5 Role of Extent and Persistence of DNA Modifications in Chemical Carcinogenesis by Aromatic Amines
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    Chapter 6 Can DNA Methylation Regulate Gene Expression?
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    Chapter 7 tRNA Alterations in Cancer
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    Chapter 8 Tumor-Specific tRNA Modifications in Mouse Plasmacytomas and Other Tumors
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    Chapter 9 Alterations in Post-Transcriptional Modification of the Y Base in Phenylalanine tRNA from Tumor Cells
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    Chapter 10 Why Is Tumor tRNA Hypomodified with Respect to Q Nucleoside?
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    Chapter 11 The effects of growth factors on tRNALys modification.
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    Chapter 12 Perturbation of the mitochondrial lysine tRNA population by virus-induced transformation or stress of mammalian cells: functional properties and nucleotide sequence of a mitochondrially associated lysine tRNA.
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    Chapter 13 Involvement of tRNA in Retrovirus Expression: Biological Implications of Reverse Transcriptase-Primer tRNA Interactions
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    Chapter 14 Enzymatic Methylation of Chicken Erythrocyte DNA Modified by Two Carcinogens, 2-(N-Acetoxyacetylamino) Fluorene and Methylnitrosourea
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    Chapter 15 Inhibition of DNA Methylation by 5-Azacytidine
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    Chapter 16 Alteration of enzymatic DNA methylation by chemical carcinogens.
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    Chapter 17 Ethionine-Induced Alterations of tRNA Metabolism
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    Chapter 18 Processing of tRNA is accomplished by a high-molecular-weight enzyme complex.
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    Chapter 19 Alteration of tRNA Modification in Eukaryotes: Causes and Consequences
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    Chapter 20 Effects of Cortisol on tRNA Methylase Activities in Rat Mammary Carcinoma
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    Chapter 21 An approach to inhibition of viral replication: inhibition of mRNA methylation.
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    Chapter 22 Specific Effects of 5-Fluoropyrimidines and 5-Azapyrimidines on Modification of the 5 Position of Pyrimidines, in Particular the Synthesis of 5-Methyluracil and 5-Methylcytosine in Nucleic Acids
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    Chapter 23 New applications of urinary nucleoside markers.
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    Chapter 24 Multivariate analysis of urinary RNA catabolites in malignancies: cross-sectional and longitudinal studies.
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    Chapter 25 Evaluation of carcinoembryonic antigen, tissue polypeptide antigen, placental alkaline phosphatase, and modified nucleosides as biological markers in malignant lymphomas.
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    Chapter 26 Quantitative High-performance Liquid Chromatography Analysis of Modified Nucleosides in Physiological Fluids, tRNA, and DNA
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    Chapter 27 Modified Nucleosides in Body Fluids of Tumor-Bearing Patients
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    Chapter 28 Increasing Urinary Levels of Modified Nucleosides and Bases During Tumor Development in Mice
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    Chapter 29 Comparison of Urinary Modified Nucleosides and Bases in Rats with Hepatomas and Nephroblastomas
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    Chapter 30 Characterization and Analysis of Oncofetal tRNA and Its Possible Application for Cancer Diagnosis and Therapy
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    Chapter 31 Excretion of polyamines by children with leukemia during chemotherapy.
Attention for Chapter 25: Evaluation of carcinoembryonic antigen, tissue polypeptide antigen, placental alkaline phosphatase, and modified nucleosides as biological markers in malignant lymphomas.
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Chapter title
Evaluation of carcinoembryonic antigen, tissue polypeptide antigen, placental alkaline phosphatase, and modified nucleosides as biological markers in malignant lymphomas.
Chapter number 25
Book title
Modified Nucleosides and Cancer
Published in
Recent results in cancer research Fortschritte der Krebsforschung Progrès dans les recherches sur le cancer, January 1983
DOI 10.1007/978-3-642-81947-6_25
Pubmed ID
Book ISBNs
978-3-64-281949-0, 978-3-64-281947-6
Authors

Rasmuson, T, Björk, G R, Damber, L, Holm, S E, Jacobsson, L, Jeppsson, A, Littbrand, B, Stigbrand, T, Westman, G, Rasmuson, T., Björk, G. R., Damber, L., Holm, S. E., Jacobsson, L., Jeppsson, A., Littbrand, B., Stigbrand, T., Westman, G.

Abstract

We have evaluated CEA, TPA, PLAP in sera from patients with three different kinds of malignant lymphomas. Six modified nucleosides, psi, m1A, m1G, m1I, m2G, and m2(2)G were analyzed in the urine from the same group of patients. The histological diagnoses were histiocytic lymphoma (21 patients), lymphocytic lymphoma (19 patients) and Hodgkin's disease (23 patients). The patients were classified into four different clinical stages. Consecutive samples were analyzed before and during ongoing radiotherapy and chemotherapy and during the post-treatment period. Our results showed that TPA and PLAP had limited value as biological markers for patients with malignant lymphomas. For CEA a possible correlation with clinical stage was observed only in patients with Hodgkin's disease. The modified nucleosides, especially psi, showed a correlation with clinical stage for patients with all three diagnoses. Elevated levels of psi in urine were in healthy adults 4%, in patients in clinical stage 1 14%, and in patients with advanced disease 62%. Six cases showed a good correlation between the change in clinical stage upon treatment and the parallel change in the level of psi in the urine. Our results suggest that modified nucleosides, especially psi, are valuable as biological markers for patients with malignant lymphomas.

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Mendeley readers

The data shown below were compiled from readership statistics for 4 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 4 100%

Demographic breakdown

Readers by professional status Count As %
Professor 1 25%
Student > Ph. D. Student 1 25%
Researcher 1 25%
Student > Master 1 25%
Readers by discipline Count As %
Medicine and Dentistry 3 75%
Social Sciences 1 25%