Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins

Background. Radiosensitizers are used in order to increase the efficacy of radiotherapy. Most of the presently known radiosensitizing agents have a poor selectivity and are not tumour-specific. Porphyrins have a selective uptake in tumour relative to the surrounding normal tissue. The aim of the pre...

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Main Authors: Laimutė RUTKOVSKIENĖ, Laima PLĖŠNIENĖ, Daiva SENDIULIENĖ, Alfonsas STANČIUS, Jurgita LIUTKEVIČIŪTĖ-NAVICKIENĖ
Format: Article
Language:English
Published: Vilnius University Press 2011-04-01
Series:Acta Medica Lituanica
Online Access:https://www.journals.vu.lt/AML/article/view/21589
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author Laimutė RUTKOVSKIENĖ
Laima PLĖŠNIENĖ
Daiva SENDIULIENĖ
Alfonsas STANČIUS
Jurgita LIUTKEVIČIŪTĖ-NAVICKIENĖ
author_facet Laimutė RUTKOVSKIENĖ
Laima PLĖŠNIENĖ
Daiva SENDIULIENĖ
Alfonsas STANČIUS
Jurgita LIUTKEVIČIŪTĖ-NAVICKIENĖ
author_sort Laimutė RUTKOVSKIENĖ
collection DOAJ
description Background. Radiosensitizers are used in order to increase the efficacy of radiotherapy. Most of the presently known radiosensitizing agents have a poor selectivity and are not tumour-specific. Porphyrins have a selective uptake in tumour relative to the surrounding normal tissue. The aim of the present work was to test the capability of two photosensitizers – hematoporphyrin derivative (HpD) or temoporfin (mTHPC) – and gamma rays to produce some kind of selective inhibition of tumour cell proliferation. Materials and methods. Dark toxicity experiments were carried out using a sensitizer concentration range 0–50 μg/ml for HpD, or 0–5 μg/ml for mTHPC. For the radiosensitized treatment of rat C6 glioma cells, HpD was added at a final concentration of 1 μg/ml and mTHPC at a final concentration of 0.1 μg/ml. The irradiation with gamma rays was performed using doses ranging from 0 to 8 Gy. Cell survival was determined using the colony forming assay. Results. HpD (1 μg/ml) and mTHPC (0.1 μg/ml) were found to have no toxic effects on C6 glioma cells. A cytotoxic dose without drugs, inducing a reduction in colony survival by 20%, was achieved at 2 Gy and by 50% at 4 Gy. The radiosensitized treatment of cells with HpD resulted in a significant (p ≤ 0.05) decline in cell survival as compared with irradiation alone. For C6 treated with mTHPC, the results did not differ between the two groups (with and without the drug). Conclusions. The results of this study have shown that mTHPC (0.1 μg/ml) does not act as a radiosensitizer, whereas HpD can act, under certain conditions, as a tumour radiosensitizer. These findings suggest that HpD is a potential agent in combination with radiation therapy of malignant gliomas. Keywords: rat C6 glioma cells, radiosensitization, porphyrins, colony forming assay
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spelling doaj.art-cb269cd8b8794d6a8f979975405149942022-12-22T03:13:25ZengVilnius University PressActa Medica Lituanica1392-01382029-41742011-04-0118210.6001/actamedica.v18i2.1816Sensitization of rat C6 glioma cells to ionizing radiation by porphyrinsLaimutė RUTKOVSKIENĖLaima PLĖŠNIENĖDaiva SENDIULIENĖAlfonsas STANČIUSJurgita LIUTKEVIČIŪTĖ-NAVICKIENĖBackground. Radiosensitizers are used in order to increase the efficacy of radiotherapy. Most of the presently known radiosensitizing agents have a poor selectivity and are not tumour-specific. Porphyrins have a selective uptake in tumour relative to the surrounding normal tissue. The aim of the present work was to test the capability of two photosensitizers – hematoporphyrin derivative (HpD) or temoporfin (mTHPC) – and gamma rays to produce some kind of selective inhibition of tumour cell proliferation. Materials and methods. Dark toxicity experiments were carried out using a sensitizer concentration range 0–50 μg/ml for HpD, or 0–5 μg/ml for mTHPC. For the radiosensitized treatment of rat C6 glioma cells, HpD was added at a final concentration of 1 μg/ml and mTHPC at a final concentration of 0.1 μg/ml. The irradiation with gamma rays was performed using doses ranging from 0 to 8 Gy. Cell survival was determined using the colony forming assay. Results. HpD (1 μg/ml) and mTHPC (0.1 μg/ml) were found to have no toxic effects on C6 glioma cells. A cytotoxic dose without drugs, inducing a reduction in colony survival by 20%, was achieved at 2 Gy and by 50% at 4 Gy. The radiosensitized treatment of cells with HpD resulted in a significant (p ≤ 0.05) decline in cell survival as compared with irradiation alone. For C6 treated with mTHPC, the results did not differ between the two groups (with and without the drug). Conclusions. The results of this study have shown that mTHPC (0.1 μg/ml) does not act as a radiosensitizer, whereas HpD can act, under certain conditions, as a tumour radiosensitizer. These findings suggest that HpD is a potential agent in combination with radiation therapy of malignant gliomas. Keywords: rat C6 glioma cells, radiosensitization, porphyrins, colony forming assayhttps://www.journals.vu.lt/AML/article/view/21589
spellingShingle Laimutė RUTKOVSKIENĖ
Laima PLĖŠNIENĖ
Daiva SENDIULIENĖ
Alfonsas STANČIUS
Jurgita LIUTKEVIČIŪTĖ-NAVICKIENĖ
Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins
Acta Medica Lituanica
title Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins
title_full Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins
title_fullStr Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins
title_full_unstemmed Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins
title_short Sensitization of rat C6 glioma cells to ionizing radiation by porphyrins
title_sort sensitization of rat c6 glioma cells to ionizing radiation by porphyrins
url https://www.journals.vu.lt/AML/article/view/21589
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