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A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation

Radiation pneumonitis (RP) is an important dose-limiting toxicity during thoracic radiotherapy. Previous investigations have shown that curcumin is used for the treatment of inflammatory conditions and cancer, suggesting that curcumin may prevent RP and sensitize cancer cells to irradiation. However...

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Autores principales: Shi, Hua-shan, Gao, Xiang, Li, Dan, Zhang, Qiong-wen, Wang, Yong-sheng, Zheng, Yu, Cai, Lu-Lu, Zhong, Ren-ming, Rui, Ao, Li, Zhi-yong, Zheng, Hao, Chen, Xian-cheng, Chen, Li-juan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368513/
https://www.ncbi.nlm.nih.gov/pubmed/22679371
http://dx.doi.org/10.2147/IJN.S31439
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author Shi, Hua-shan
Gao, Xiang
Li, Dan
Zhang, Qiong-wen
Wang, Yong-sheng
Zheng, Yu
Cai, Lu-Lu
Zhong, Ren-ming
Rui, Ao
Li, Zhi-yong
Zheng, Hao
Chen, Xian-cheng
Chen, Li-juan
author_facet Shi, Hua-shan
Gao, Xiang
Li, Dan
Zhang, Qiong-wen
Wang, Yong-sheng
Zheng, Yu
Cai, Lu-Lu
Zhong, Ren-ming
Rui, Ao
Li, Zhi-yong
Zheng, Hao
Chen, Xian-cheng
Chen, Li-juan
author_sort Shi, Hua-shan
collection PubMed
description Radiation pneumonitis (RP) is an important dose-limiting toxicity during thoracic radiotherapy. Previous investigations have shown that curcumin is used for the treatment of inflammatory conditions and cancer, suggesting that curcumin may prevent RP and sensitize cancer cells to irradiation. However, the clinical advancement of curcumin is limited by its poor water solubility and low bioavailability after oral administration. Here, a water-soluble liposomal curcumin system was developed to investigate its prevention and sensitizing effects by an intravenous administration manner in mice models. The results showed that liposomal curcumin inhibited nuclear factor-κB pathway and downregulated inflammatory factors including tumor necrosis factor-α, interleukin (IL)-6, IL-8, and transforming growth factor-β induced by thoracic irradiation. Furthermore, the combined treatment with liposomal curcumin and radiotherapy increased intratumoral apoptosis and microvessel responses to irradiation in vivo. The significantly enhanced inhibition of tumor growth also was observed in a murine lung carcinoma (LL/2) model. There were no obvious toxicities observed in mice. The current results indicate that liposomal curcumin can effectively mitigate RP, reduce the fibrosis of lung, and sensitize LL/2 cells to irradiation. This study also suggests that the systemic administration of liposomal curcumin is safe and deserves to be investigated for further clinical application.
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spelling pubmed-33685132012-06-07 A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation Shi, Hua-shan Gao, Xiang Li, Dan Zhang, Qiong-wen Wang, Yong-sheng Zheng, Yu Cai, Lu-Lu Zhong, Ren-ming Rui, Ao Li, Zhi-yong Zheng, Hao Chen, Xian-cheng Chen, Li-juan Int J Nanomedicine Original Research Radiation pneumonitis (RP) is an important dose-limiting toxicity during thoracic radiotherapy. Previous investigations have shown that curcumin is used for the treatment of inflammatory conditions and cancer, suggesting that curcumin may prevent RP and sensitize cancer cells to irradiation. However, the clinical advancement of curcumin is limited by its poor water solubility and low bioavailability after oral administration. Here, a water-soluble liposomal curcumin system was developed to investigate its prevention and sensitizing effects by an intravenous administration manner in mice models. The results showed that liposomal curcumin inhibited nuclear factor-κB pathway and downregulated inflammatory factors including tumor necrosis factor-α, interleukin (IL)-6, IL-8, and transforming growth factor-β induced by thoracic irradiation. Furthermore, the combined treatment with liposomal curcumin and radiotherapy increased intratumoral apoptosis and microvessel responses to irradiation in vivo. The significantly enhanced inhibition of tumor growth also was observed in a murine lung carcinoma (LL/2) model. There were no obvious toxicities observed in mice. The current results indicate that liposomal curcumin can effectively mitigate RP, reduce the fibrosis of lung, and sensitize LL/2 cells to irradiation. This study also suggests that the systemic administration of liposomal curcumin is safe and deserves to be investigated for further clinical application. Dove Medical Press 2012 2012-05-24 /pmc/articles/PMC3368513/ /pubmed/22679371 http://dx.doi.org/10.2147/IJN.S31439 Text en © 2012 Shi et al, publisher and licensee Dove Medical Press Ltd. This is an Open Access article which permits unrestricted noncommercial use, provided the original work is properly cited.
spellingShingle Original Research
Shi, Hua-shan
Gao, Xiang
Li, Dan
Zhang, Qiong-wen
Wang, Yong-sheng
Zheng, Yu
Cai, Lu-Lu
Zhong, Ren-ming
Rui, Ao
Li, Zhi-yong
Zheng, Hao
Chen, Xian-cheng
Chen, Li-juan
A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
title A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
title_full A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
title_fullStr A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
title_full_unstemmed A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
title_short A systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
title_sort systemic administration of liposomal curcumin inhibits radiation pneumonitis and sensitizes lung carcinoma to radiation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368513/
https://www.ncbi.nlm.nih.gov/pubmed/22679371
http://dx.doi.org/10.2147/IJN.S31439
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