Literature DB >> 7392649

Biological markers in breast carcinoma--clinical correlations with pseudouridine, N2,N2-dimethylguanosine, and 1-methylinosine.

D C Tormey, T P Waalkes, C W Gehrke.   

Abstract

Urinary levels of the minor nucleosides, pseudouridine (psi),N2, N2-dimethylguanosine (m22G), and 1-methylinosine (m1I), were investigated in patients with breast carcinoma. Elevated levels of psi were observed in 27/131 (20.6%) patients with metastatic disease, 1/14 (7.1%) preoperative patients, and 1/28 (3.6%) postoperative N+ patients. Elevated levels of m22G and M1I were observed, respectively, in 46/131 (35.1%) and 274131 (20.6%) patients with metastatic disease, 3/14 (21.4%) and 3/14 preoperative patients, and 6/28 (21.4%) and 2/28 (7.1%) postoperative N+ patients. There was no correlation between nucleoside levels and involvement of specific organ sites with metastatic disease, nor with chemotherapy response rate or time to treatment failure. During the treatment of metastatic disease there was a tendency for elevated pretherapy psi levels to decrease with attainment of a response and, if the levels subsequently rose to be associated with treatment failure. However, increasing levels of m22G and 71I occurred with both response and disease progression. These results suggest that routine measurement of the level of the urinary nucleosides would be of limited value for following the disease course in patients with breast cancer.

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Year:  1980        PMID: 7392649     DOI: 10.1002/jso.2930140313

Source DB:  PubMed          Journal:  J Surg Oncol        ISSN: 0022-4790            Impact factor:   3.454


  6 in total

1.  Plasma metabolomics exhibit response to therapy in chronic thromboembolic pulmonary hypertension.

Authors:  Emilia M Swietlik; Pavandeep Ghataorhe; Kasia I Zalewska; John Wharton; Luke S Howard; Dolores Taboada; John E Cannon; Nicholas W Morrell; Martin R Wilkins; Mark Toshner; Joanna Pepke-Zaba; Christopher J Rhodes
Journal:  Eur Respir J       Date:  2021-04-01       Impact factor: 16.671

2.  MALDI-TOF MS analysis of urinary nucleosides.

Authors:  Bernd Kammerer; Antje Frickenschmidt; Christoph H Gleiter; Stefan Laufer; Hartmut Liebich
Journal:  J Am Soc Mass Spectrom       Date:  2005-04-20       Impact factor: 3.109

3.  Targeted Profiling of Epitranscriptomic Reader, Writer, and Eraser Proteins Accompanied with Radioresistance in Breast Cancer Cells.

Authors:  Tianyu F Qi; Weili Miao; Yinsheng Wang
Journal:  Anal Chem       Date:  2022-01-12       Impact factor: 6.986

4.  Identification of urinary modified nucleosides and ribosylated metabolites in humans via combined ESI-FTICR MS and ESI-IT MS analysis.

Authors:  Dino Bullinger; Richard Fux; Graeme Nicholson; Stefan Plontke; Claus Belka; Stefan Laufer; Christoph H Gleiter; Bernd Kammerer
Journal:  J Am Soc Mass Spectrom       Date:  2008-06-28       Impact factor: 3.109

5.  Prediction of breast cancer by profiling of urinary RNA metabolites using Support Vector Machine-based feature selection.

Authors:  Carsten Henneges; Dino Bullinger; Richard Fux; Natascha Friese; Harald Seeger; Hans Neubauer; Stefan Laufer; Christoph H Gleiter; Matthias Schwab; Andreas Zell; Bernd Kammerer
Journal:  BMC Cancer       Date:  2009-04-05       Impact factor: 4.430

6.  Metabolic signature of breast cancer cell line MCF-7: profiling of modified nucleosides via LC-IT MS coupling.

Authors:  Dino Bullinger; Hans Neubauer; Tanja Fehm; Stefan Laufer; Christoph H Gleiter; Bernd Kammerer
Journal:  BMC Biochem       Date:  2007-11-29       Impact factor: 4.059

  6 in total

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