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Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice

Radiotherapy alone has several limitations for treating lung cancer. Inhalation, a non-invasive approach for direct delivery of therapeutic agents to the lung, may help to enhance the therapeutic efficacy of radiation. Up-regulating beclin1, known as a tumor suppressor gene that plays a major role i...

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Autores principales: Shin, Ji-Young, Lim, Hwang-Tae, Minai-Tehrani, Arash, Noh, Mi-Suk, Kim, Ji-Eun, Kim, Ji-Hye, Jiang, Hu-Lin, Arote, Rohidas, Kim, Doo-Yeol, Chae, Chanhee, Lee, Kee-Ho, Kim, Mi-Sook, Cho, Myung-Haing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393344/
https://www.ncbi.nlm.nih.gov/pubmed/22843615
http://dx.doi.org/10.1093/jrr/rrs005
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author Shin, Ji-Young
Lim, Hwang-Tae
Minai-Tehrani, Arash
Noh, Mi-Suk
Kim, Ji-Eun
Kim, Ji-Hye
Jiang, Hu-Lin
Arote, Rohidas
Kim, Doo-Yeol
Chae, Chanhee
Lee, Kee-Ho
Kim, Mi-Sook
Cho, Myung-Haing
author_facet Shin, Ji-Young
Lim, Hwang-Tae
Minai-Tehrani, Arash
Noh, Mi-Suk
Kim, Ji-Eun
Kim, Ji-Hye
Jiang, Hu-Lin
Arote, Rohidas
Kim, Doo-Yeol
Chae, Chanhee
Lee, Kee-Ho
Kim, Mi-Sook
Cho, Myung-Haing
author_sort Shin, Ji-Young
collection PubMed
description Radiotherapy alone has several limitations for treating lung cancer. Inhalation, a non-invasive approach for direct delivery of therapeutic agents to the lung, may help to enhance the therapeutic efficacy of radiation. Up-regulating beclin1, known as a tumor suppressor gene that plays a major role in autophagy, may sensitize tumors and lead to tumor regression in lungs of K-ras(LA1) lung cancer model mice. To minimize the side-effects of radiotherapy, fractionated exposures (five times, 24-h interval) with low dose (2 Gy) of radiation to the restricted area (thorax, 2 cm) were conducted. After sensitizing the lungs with radiation, beclin1, complexed with a nano-sized biodegradable poly(ester amine), was prepared and delivered into the murine lung via aerosol three times/week for four weeks. In a histopathological analysis, animals treated with beclin1 and radiation showed highly significant tumor regression and low progression to adenocarcinoma. An increase in the number of autophagic vacuoles and secondary lysosomes was detected. Dissociation of beclin1-bcl2 stimulated autophagy activation and showed a synergistic anti-tumor effect by inhibiting the Akt-mTOR pathway, cell proliferation and angiogenesis. The combination of radiation with non-invasive aerosol delivery of beclin1 may provide a prospect for developing novel therapy regimens applicable in clinics.
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spelling pubmed-33933442013-07-01 Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice Shin, Ji-Young Lim, Hwang-Tae Minai-Tehrani, Arash Noh, Mi-Suk Kim, Ji-Eun Kim, Ji-Hye Jiang, Hu-Lin Arote, Rohidas Kim, Doo-Yeol Chae, Chanhee Lee, Kee-Ho Kim, Mi-Sook Cho, Myung-Haing J Radiat Res Biology Radiotherapy alone has several limitations for treating lung cancer. Inhalation, a non-invasive approach for direct delivery of therapeutic agents to the lung, may help to enhance the therapeutic efficacy of radiation. Up-regulating beclin1, known as a tumor suppressor gene that plays a major role in autophagy, may sensitize tumors and lead to tumor regression in lungs of K-ras(LA1) lung cancer model mice. To minimize the side-effects of radiotherapy, fractionated exposures (five times, 24-h interval) with low dose (2 Gy) of radiation to the restricted area (thorax, 2 cm) were conducted. After sensitizing the lungs with radiation, beclin1, complexed with a nano-sized biodegradable poly(ester amine), was prepared and delivered into the murine lung via aerosol three times/week for four weeks. In a histopathological analysis, animals treated with beclin1 and radiation showed highly significant tumor regression and low progression to adenocarcinoma. An increase in the number of autophagic vacuoles and secondary lysosomes was detected. Dissociation of beclin1-bcl2 stimulated autophagy activation and showed a synergistic anti-tumor effect by inhibiting the Akt-mTOR pathway, cell proliferation and angiogenesis. The combination of radiation with non-invasive aerosol delivery of beclin1 may provide a prospect for developing novel therapy regimens applicable in clinics. Oxford University Press 2012-07 2012-06-06 /pmc/articles/PMC3393344/ /pubmed/22843615 http://dx.doi.org/10.1093/jrr/rrs005 Text en © The Author 2012. Published by Oxford University Press on behalf of The Japan Radiation Research Society and Japanese Society for Therapeutic Radiology and Oncology. http://creativecommons.org/licenses/by-nc/2.5/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Biology
Shin, Ji-Young
Lim, Hwang-Tae
Minai-Tehrani, Arash
Noh, Mi-Suk
Kim, Ji-Eun
Kim, Ji-Hye
Jiang, Hu-Lin
Arote, Rohidas
Kim, Doo-Yeol
Chae, Chanhee
Lee, Kee-Ho
Kim, Mi-Sook
Cho, Myung-Haing
Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice
title Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice
title_full Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice
title_fullStr Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice
title_full_unstemmed Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice
title_short Aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of K-ras(LA1) mice
title_sort aerosol delivery of beclin1 enhanced the anti-tumor effect of radiation in the lungs of k-ras(la1) mice
topic Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393344/
https://www.ncbi.nlm.nih.gov/pubmed/22843615
http://dx.doi.org/10.1093/jrr/rrs005
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