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Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy
Magnetic resonance spectroscopy in situ was used to study changes in phosphorus 31 metabolism after photodynamic therapy (PDT) of transplanted HeLa cell tumours. Tumours were irradiated 2 h after administration of ATX-S10 (8-formyloximethylidene-7-hydroxy-3-ethenyl-2,7,12,18, tetramethyl-porphyrin-1...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1999
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363014/ https://www.ncbi.nlm.nih.gov/pubmed/10389989 http://dx.doi.org/10.1038/sj.bjc.6690332 |
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author | Nishiwaki, M Fujise, Y Yoshida, T O Matsuzawa, E Nishiwaki, Y |
author_facet | Nishiwaki, M Fujise, Y Yoshida, T O Matsuzawa, E Nishiwaki, Y |
author_sort | Nishiwaki, M |
collection | PubMed |
description | Magnetic resonance spectroscopy in situ was used to study changes in phosphorus 31 metabolism after photodynamic therapy (PDT) of transplanted HeLa cell tumours. Tumours were irradiated 2 h after administration of ATX-S10 (8-formyloximethylidene-7-hydroxy-3-ethenyl-2,7,12,18, tetramethyl-porphyrin-13,17-bispropionil aspartate), a new photosensitizer and chlorin derivative. Nuclear magnetic resonance spectra were measured prior to illumination and 1, 3, 7, 14, 21 and 28 days after PDT on each mouse. A drastic decrease in adenosine triphosphate (ATP) and a concomitant increase in inorganic phosphate (Pi) were evident on the first day after PDT in all cases. The β-ATP/total phosphate (P) ratio was 0.64 ± 0.29% (average ± s.d.) in complete response, 0.67 ± 0.30% in recurrence and 2.45 ± 0.93% in partial response. Comparison of this ratio to the histological findings revealed that the β-ATP/total P ratio reflects the HeLa cell tumours which survived PDT. In other words, partial response on the one hand was distinguished from complete response and recurrence on the other with this ratio 1 day after PDT (P < 0.05). In addition, the ratio of phosphomonoester (PME) to Pi rose beyond 1.0 when macroscopic recurrence occurred, while it stayed under 1.0 in complete response. This finding suggests that the recurrence of HeLa cell tumours can be detected by the PME/Pi ratio. © 1999 Cancer Research Campaign |
format | Text |
id | pubmed-2363014 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1999 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23630142009-09-10 Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy Nishiwaki, M Fujise, Y Yoshida, T O Matsuzawa, E Nishiwaki, Y Br J Cancer Regular Article Magnetic resonance spectroscopy in situ was used to study changes in phosphorus 31 metabolism after photodynamic therapy (PDT) of transplanted HeLa cell tumours. Tumours were irradiated 2 h after administration of ATX-S10 (8-formyloximethylidene-7-hydroxy-3-ethenyl-2,7,12,18, tetramethyl-porphyrin-13,17-bispropionil aspartate), a new photosensitizer and chlorin derivative. Nuclear magnetic resonance spectra were measured prior to illumination and 1, 3, 7, 14, 21 and 28 days after PDT on each mouse. A drastic decrease in adenosine triphosphate (ATP) and a concomitant increase in inorganic phosphate (Pi) were evident on the first day after PDT in all cases. The β-ATP/total phosphate (P) ratio was 0.64 ± 0.29% (average ± s.d.) in complete response, 0.67 ± 0.30% in recurrence and 2.45 ± 0.93% in partial response. Comparison of this ratio to the histological findings revealed that the β-ATP/total P ratio reflects the HeLa cell tumours which survived PDT. In other words, partial response on the one hand was distinguished from complete response and recurrence on the other with this ratio 1 day after PDT (P < 0.05). In addition, the ratio of phosphomonoester (PME) to Pi rose beyond 1.0 when macroscopic recurrence occurred, while it stayed under 1.0 in complete response. This finding suggests that the recurrence of HeLa cell tumours can be detected by the PME/Pi ratio. © 1999 Cancer Research Campaign Nature Publishing Group 1999-04 /pmc/articles/PMC2363014/ /pubmed/10389989 http://dx.doi.org/10.1038/sj.bjc.6690332 Text en Copyright © 1999 Cancer Research Campaign 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 | Regular Article Nishiwaki, M Fujise, Y Yoshida, T O Matsuzawa, E Nishiwaki, Y Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
title | Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
title_full | Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
title_fullStr | Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
title_full_unstemmed | Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
title_short | Evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
title_sort | evaluation of the effects of photodynamic therapy with phosphorus 31 magnetic resonance spectroscopy |
topic | Regular Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2363014/ https://www.ncbi.nlm.nih.gov/pubmed/10389989 http://dx.doi.org/10.1038/sj.bjc.6690332 |
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