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Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment

The effects of combined and simultaneously applied localised 43°C hyperthermia (HT) and an antivascular bacteriochlorophyll-serine-based photodynamic therapy (Bchl-ser-PDT) on tumour growth and several microenvironmental parameters were examined. Rats bearing DS-sarcomas were allocated to treatment...

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Autores principales: Kelleher, D K, Thews, O, Scherz, A, Salomon, Y, Vaupel, P
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395271/
https://www.ncbi.nlm.nih.gov/pubmed/14676815
http://dx.doi.org/10.1038/sj.bjc.6601457
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author Kelleher, D K
Thews, O
Scherz, A
Salomon, Y
Vaupel, P
author_facet Kelleher, D K
Thews, O
Scherz, A
Salomon, Y
Vaupel, P
author_sort Kelleher, D K
collection PubMed
description The effects of combined and simultaneously applied localised 43°C hyperthermia (HT) and an antivascular bacteriochlorophyll-serine-based photodynamic therapy (Bchl-ser-PDT) on tumour growth and several microenvironmental parameters were examined. Rats bearing DS-sarcomas were allocated to treatment groups: (i) sham-treatment (control), (ii) Bchl-ser-PDT (20 mg kg(−1) i.v.), (iii) localised HT, (iv) Bchl-ser-PDT+HT. The light source used was an infrared-A irradiator, which, by use of appropriate filters, delivered the different ranges of wavelengths required. Following treatment, tumour volume was monitored. The greatest tumour growth inhibition was seen with Bchl-ser-PDT+HT, and subsequent experiments identified the pathophysiological basis for this effect. Red blood cell flux in tumour microvessels declined rapidly upon Bchl-ser-PDT+HT, reaching approximately 10% of initial values by the end of treatment. Similarly, tumour oxygenation worsened, reaching almost anoxic levels by the end of the treatment period. Assessment of metabolic parameters showed a pronounced increase in lactate levels and a decrease in ATP concentrations after combined treatment. The results presented suggest that vascular collapse and flow stasis resulting in a deterioration of tumour oxygenation and a switch from oxidative to glycolytic glucose turnover are key elements in the tumour eradication seen with this novel approach in which an antivascular PDT and HT are combined and simultaneously applied.
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spelling pubmed-23952712009-09-10 Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment Kelleher, D K Thews, O Scherz, A Salomon, Y Vaupel, P Br J Cancer Experimental Therapeutic The effects of combined and simultaneously applied localised 43°C hyperthermia (HT) and an antivascular bacteriochlorophyll-serine-based photodynamic therapy (Bchl-ser-PDT) on tumour growth and several microenvironmental parameters were examined. Rats bearing DS-sarcomas were allocated to treatment groups: (i) sham-treatment (control), (ii) Bchl-ser-PDT (20 mg kg(−1) i.v.), (iii) localised HT, (iv) Bchl-ser-PDT+HT. The light source used was an infrared-A irradiator, which, by use of appropriate filters, delivered the different ranges of wavelengths required. Following treatment, tumour volume was monitored. The greatest tumour growth inhibition was seen with Bchl-ser-PDT+HT, and subsequent experiments identified the pathophysiological basis for this effect. Red blood cell flux in tumour microvessels declined rapidly upon Bchl-ser-PDT+HT, reaching approximately 10% of initial values by the end of treatment. Similarly, tumour oxygenation worsened, reaching almost anoxic levels by the end of the treatment period. Assessment of metabolic parameters showed a pronounced increase in lactate levels and a decrease in ATP concentrations after combined treatment. The results presented suggest that vascular collapse and flow stasis resulting in a deterioration of tumour oxygenation and a switch from oxidative to glycolytic glucose turnover are key elements in the tumour eradication seen with this novel approach in which an antivascular PDT and HT are combined and simultaneously applied. Nature Publishing Group 2003-12-15 2003-12-09 /pmc/articles/PMC2395271/ /pubmed/14676815 http://dx.doi.org/10.1038/sj.bjc.6601457 Text en Copyright © 2003 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 Therapeutic
Kelleher, D K
Thews, O
Scherz, A
Salomon, Y
Vaupel, P
Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
title Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
title_full Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
title_fullStr Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
title_full_unstemmed Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
title_short Combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
title_sort combined hyperthermia and chlorophyll-based photodynamic therapy: tumour growth and metabolic microenvironment
topic Experimental Therapeutic
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2395271/
https://www.ncbi.nlm.nih.gov/pubmed/14676815
http://dx.doi.org/10.1038/sj.bjc.6601457
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