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Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation

Photodynamic therapy is a cancer treatment based on the interaction of light, oxygen and a photosensitiser. Protoporphyrin. IX is an endogenous photosensitiser derived from the pro-drug aminolaevulinic acid. Tumours contain areas of hypoxia and hypoglycaemia. Tumour cells adapt to these conditions b...

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Autores principales: Wyld, L, Tomlinson, M, Reed, M W R, Brown, N J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375344/
https://www.ncbi.nlm.nih.gov/pubmed/11953896
http://dx.doi.org/10.1038/sj.bjc.6600234
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author Wyld, L
Tomlinson, M
Reed, M W R
Brown, N J
author_facet Wyld, L
Tomlinson, M
Reed, M W R
Brown, N J
author_sort Wyld, L
collection PubMed
description Photodynamic therapy is a cancer treatment based on the interaction of light, oxygen and a photosensitiser. Protoporphyrin. IX is an endogenous photosensitiser derived from the pro-drug aminolaevulinic acid. Tumours contain areas of hypoxia and hypoglycaemia. Tumour cells adapt to these conditions by stress protein induction which may induce resistance to cancer therapies. The effect of chronic hypoglycaemia on sensitivity to aminolaevulinic acid-induced photodynamic therapy in vitro was studied in MCF-7, human breast cancer cells. Following chronic exposure to 0, 1 or 25 mM, glucose, cells were treated with aminolaevulinic acid and the generation of intracellular protoporphyrin. IX measured by spectrofluorimetry. Aminolaevulinic acid-induced photodynamic therapy sensitivity was compared between cells following chronic exposure to 0, 1 or 25 mM glucose. Percentage cell survival was determined by clonogenic assay. Cells cultured in low glucose generated higher levels of protoporphyrin IX compared to standard glucose medium (0 mM glucose: 0.88×10(−5) ng cell(−1), 1 mM: 0.86×10(−5) ng cell(−1), 25 mM: 0.605×10(−5) ng cell(−1), P<0.05). However, photodynamic therapy sensitivity was reduced in glucose deprived cells (0 mM glucose: 61% survival, 1 mM: 80.5% and 25 mM: 39.6%, P<0.05). Chronic exposure to low glucose induces photodynamic therapy resistance despite increased intracellular concentrations of protoporphyrin IX and may reflect cellular adaptation to chronic glucose deprivation. British Journal of Cancer (2002) 86, 1343–1347. DOI: 10.1038/sj/bjc/6600234 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23753442009-09-10 Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation Wyld, L Tomlinson, M Reed, M W R Brown, N J Br J Cancer Experimental Therapeutics Photodynamic therapy is a cancer treatment based on the interaction of light, oxygen and a photosensitiser. Protoporphyrin. IX is an endogenous photosensitiser derived from the pro-drug aminolaevulinic acid. Tumours contain areas of hypoxia and hypoglycaemia. Tumour cells adapt to these conditions by stress protein induction which may induce resistance to cancer therapies. The effect of chronic hypoglycaemia on sensitivity to aminolaevulinic acid-induced photodynamic therapy in vitro was studied in MCF-7, human breast cancer cells. Following chronic exposure to 0, 1 or 25 mM, glucose, cells were treated with aminolaevulinic acid and the generation of intracellular protoporphyrin. IX measured by spectrofluorimetry. Aminolaevulinic acid-induced photodynamic therapy sensitivity was compared between cells following chronic exposure to 0, 1 or 25 mM glucose. Percentage cell survival was determined by clonogenic assay. Cells cultured in low glucose generated higher levels of protoporphyrin IX compared to standard glucose medium (0 mM glucose: 0.88×10(−5) ng cell(−1), 1 mM: 0.86×10(−5) ng cell(−1), 25 mM: 0.605×10(−5) ng cell(−1), P<0.05). However, photodynamic therapy sensitivity was reduced in glucose deprived cells (0 mM glucose: 61% survival, 1 mM: 80.5% and 25 mM: 39.6%, P<0.05). Chronic exposure to low glucose induces photodynamic therapy resistance despite increased intracellular concentrations of protoporphyrin IX and may reflect cellular adaptation to chronic glucose deprivation. British Journal of Cancer (2002) 86, 1343–1347. DOI: 10.1038/sj/bjc/6600234 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-04-22 /pmc/articles/PMC2375344/ /pubmed/11953896 http://dx.doi.org/10.1038/sj.bjc.6600234 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
Wyld, L
Tomlinson, M
Reed, M W R
Brown, N J
Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
title Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
title_full Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
title_fullStr Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
title_full_unstemmed Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
title_short Aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
title_sort aminolaevulinic acid-induced photodynamic therapy: cellular responses to glucose starvation
topic Experimental Therapeutics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375344/
https://www.ncbi.nlm.nih.gov/pubmed/11953896
http://dx.doi.org/10.1038/sj.bjc.6600234
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