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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 23: New applications of urinary nucleoside markers.
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Chapter title
New applications of urinary nucleoside markers.
Chapter number 23
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_23
Pubmed ID
Book ISBNs
978-3-64-281949-0, 978-3-64-281947-6
Authors

Borek, E, Sharma, O K, Waalkes, T P, Borek, E., Sharma, O. K., Waalkes, T. P.

Abstract

In order to extend the usefulness of the quantitation of urinary nucleoside markers, studies were undertaken to explore the adaptability of such determinations for early detection in cancer-prone populations such as asbestos workers. Another study was aimed at exploring the usefulness of therapy in individual patients. During these studies, two heretofore unknown phenomena serendipitously emerged which expand the versatility of the marker determinations: (a) radiation damage in animals and humans causes an excretion of urinary BAIB which from preliminary studies appears to be proportional to the irradiation burden, and (b) lead poisoning in the human also produces BAIB excretion. Some of the practical uses of these determinations are self-evident. Among 13 asbestos workers without clinical symptoms, eight were found to have significant elevations of the marker levels. Nine asbestos workers with diagnosed mesothelioma all excreted two or more markers at high levels. Some of the psi levels were the highest seen. Currently the diagnosis of mesothelioma is difficult and painful, requiring a rib resection; however, an asbestos worker with such elevations--provided small cell carcinoma of the lung is ruled out--can be seriously suspected of having mesothelioma. In a study of the usefulness of the markers in following therapy of trophoblastic disease, these markers were determined in women with incipient invasive hydatidiform mole. After curettage, the nucleoside markers indicated absence of residual disease but the usual marker, HCG, was still markedly elevated. The women were followed up for 2 years and were found to remain symptom-free. Therefore the source of the nucleoside markers is cleared more rapidly than that of HCG.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 13 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 13 100%

Demographic breakdown

Readers by professional status Count As %
Researcher 7 54%
Other 2 15%
Librarian 1 8%
Student > Master 1 8%
Student > Bachelor 1 8%
Other 0 0%
Unknown 1 8%
Readers by discipline Count As %
Medicine and Dentistry 6 46%
Philosophy 1 8%
Pharmacology, Toxicology and Pharmaceutical Science 1 8%
Nursing and Health Professions 1 8%
Biochemistry, Genetics and Molecular Biology 1 8%
Other 2 15%
Unknown 1 8%