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Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study

Ovarian carcinomas represent a major form of gynaecological malignancies, whose treatment consists mainly of surgery and chemotherapy. Besides the difficulty of prognosis, therapy of ovarian carcinomas has reached scarce improvement, as a consequence of lack of efficacy and development of drug-resis...

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Autores principales: Ferretti, A, D'Ascenzo, S, Knijn, A, Iorio, E, Dolo, V, Pavan, A, Podo, F
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364195/
https://www.ncbi.nlm.nih.gov/pubmed/11953869
http://dx.doi.org/10.1038/sj.bjc.6600189
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author Ferretti, A
D'Ascenzo, S
Knijn, A
Iorio, E
Dolo, V
Pavan, A
Podo, F
author_facet Ferretti, A
D'Ascenzo, S
Knijn, A
Iorio, E
Dolo, V
Pavan, A
Podo, F
author_sort Ferretti, A
collection PubMed
description Ovarian carcinomas represent a major form of gynaecological malignancies, whose treatment consists mainly of surgery and chemotherapy. Besides the difficulty of prognosis, therapy of ovarian carcinomas has reached scarce improvement, as a consequence of lack of efficacy and development of drug-resistance. The need of different biochemical and functional parameters has grown, in order to obtain a larger view on processes of biological and clinical significance. In this paper we report novel metabolic features detected in a series of different human ovary carcinoma lines, by (1)H NMR spectroscopy of intact cells and their extracts. Most importantly, a new ovarian adenocarcinoma line CABA I, showed strong signals in the spectral region between 3.5 and 4.0 p.p.m., assigned for the first time to the polyol sorbitol (39±11 nmol/10(6) cells). (13)C NMR analyses of these cells incubated with [1-(13)C]-D-glucose demonstrated labelled-sorbitol formation. The other ovarian carcinoma cell lines (OVCAR-3, IGROV 1, SK-OV-3 and OVCA432), showed, in the same spectral region, intense resonances from other metabolites: glutathione (up to 30 nmol/10(6) cells) and myo-inositol (up to 50 nmol/10(6) cells). Biochemical and biological functions are suggested for these compounds in human ovarian carcinoma cells, especially in relation to their possible role in cell detoxification mechanisms during tumour progression. British Journal of Cancer (2002) 86, 1180–1187. DOI: 10.1038/sj/bjc/6600189 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23641952009-09-10 Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study Ferretti, A D'Ascenzo, S Knijn, A Iorio, E Dolo, V Pavan, A Podo, F Br J Cancer Experimental Therapeutics Ovarian carcinomas represent a major form of gynaecological malignancies, whose treatment consists mainly of surgery and chemotherapy. Besides the difficulty of prognosis, therapy of ovarian carcinomas has reached scarce improvement, as a consequence of lack of efficacy and development of drug-resistance. The need of different biochemical and functional parameters has grown, in order to obtain a larger view on processes of biological and clinical significance. In this paper we report novel metabolic features detected in a series of different human ovary carcinoma lines, by (1)H NMR spectroscopy of intact cells and their extracts. Most importantly, a new ovarian adenocarcinoma line CABA I, showed strong signals in the spectral region between 3.5 and 4.0 p.p.m., assigned for the first time to the polyol sorbitol (39±11 nmol/10(6) cells). (13)C NMR analyses of these cells incubated with [1-(13)C]-D-glucose demonstrated labelled-sorbitol formation. The other ovarian carcinoma cell lines (OVCAR-3, IGROV 1, SK-OV-3 and OVCA432), showed, in the same spectral region, intense resonances from other metabolites: glutathione (up to 30 nmol/10(6) cells) and myo-inositol (up to 50 nmol/10(6) cells). Biochemical and biological functions are suggested for these compounds in human ovarian carcinoma cells, especially in relation to their possible role in cell detoxification mechanisms during tumour progression. British Journal of Cancer (2002) 86, 1180–1187. DOI: 10.1038/sj/bjc/6600189 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-04-08 /pmc/articles/PMC2364195/ /pubmed/11953869 http://dx.doi.org/10.1038/sj.bjc.6600189 Text en Copyright © 2002 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 Experimental Therapeutics
Ferretti, A
D'Ascenzo, S
Knijn, A
Iorio, E
Dolo, V
Pavan, A
Podo, F
Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study
title Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study
title_full Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study
title_fullStr Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study
title_full_unstemmed Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study
title_short Detection of polyol accumulation in a new ovarian carcinoma cell line, CABA I: a(1)H NMR study
title_sort detection of polyol accumulation in a new ovarian carcinoma cell line, caba i: a(1)h nmr study
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364195/
https://www.ncbi.nlm.nih.gov/pubmed/11953869
http://dx.doi.org/10.1038/sj.bjc.6600189
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