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Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131

Curcumin is a natural product widely consumed by humans. It has many biological properties. In this study, we investigated the radiosensitive effect of curcumin on thyroid cancer cells against cellular toxicity induced by 131-I. Human thyroid cancer and human non-malignant fibroblast cells (HFFF2) w...

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Detalles Bibliográficos
Autores principales: Hosseinimehr, Seyed Jalal, Hosseini, Seyed Amir Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Slovak Toxicology Society SETOX 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427719/
https://www.ncbi.nlm.nih.gov/pubmed/26109883
http://dx.doi.org/10.2478/intox-2014-0011
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author Hosseinimehr, Seyed Jalal
Hosseini, Seyed Amir Hossein
author_facet Hosseinimehr, Seyed Jalal
Hosseini, Seyed Amir Hossein
author_sort Hosseinimehr, Seyed Jalal
collection PubMed
description Curcumin is a natural product widely consumed by humans. It has many biological properties. In this study, we investigated the radiosensitive effect of curcumin on thyroid cancer cells against cellular toxicity induced by 131-I. Human thyroid cancer and human non-malignant fibroblast cells (HFFF2) were treated with 131-I and/or curcumin at different concentrations (5, 10 and 25 µg/ml) for 48 h. The cell proliferation was measured by determination of the surviving cells by using MTT assay. Our results showed that curcumin increased the killing effect of 131-I on thyroid cancer cells, while it exerted no toxicity on HFFF2 cells. This result shows a promising effect of curcumin on the enhancement of therapeutic effects of 131-I in patients.
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spelling pubmed-44277192015-06-24 Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131 Hosseinimehr, Seyed Jalal Hosseini, Seyed Amir Hossein Interdiscip Toxicol Original Article Curcumin is a natural product widely consumed by humans. It has many biological properties. In this study, we investigated the radiosensitive effect of curcumin on thyroid cancer cells against cellular toxicity induced by 131-I. Human thyroid cancer and human non-malignant fibroblast cells (HFFF2) were treated with 131-I and/or curcumin at different concentrations (5, 10 and 25 µg/ml) for 48 h. The cell proliferation was measured by determination of the surviving cells by using MTT assay. Our results showed that curcumin increased the killing effect of 131-I on thyroid cancer cells, while it exerted no toxicity on HFFF2 cells. This result shows a promising effect of curcumin on the enhancement of therapeutic effects of 131-I in patients. Slovak Toxicology Society SETOX 2014-06 2014-11-15 /pmc/articles/PMC4427719/ /pubmed/26109883 http://dx.doi.org/10.2478/intox-2014-0011 Text en Copyright © 2014 SETOX & Institute of Experimental Pharmacology and Toxicology, SASc. http://creativecommons.org/licenses/by/2.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hosseinimehr, Seyed Jalal
Hosseini, Seyed Amir Hossein
Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
title Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
title_full Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
title_fullStr Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
title_full_unstemmed Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
title_short Radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
title_sort radiosensitive effect of curcumin on thyroid cancer cell death induced by radioiodine-131
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4427719/
https://www.ncbi.nlm.nih.gov/pubmed/26109883
http://dx.doi.org/10.2478/intox-2014-0011
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