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Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy
PURPOSE: This study aims to investigate the effect of splenectomy on radiation-mediated growth inhibition and immune modulation in lung cancer xenograft models. MATERIALS AND METHODS: Human non-small cell lung cancer H1299 cells and murine Lewis lung carcinoma LL/2-luc cells were injected into the r...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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The Korean Society for Radiation Oncology
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984136/ https://www.ncbi.nlm.nih.gov/pubmed/35368201 http://dx.doi.org/10.3857/roj.2021.00885 |
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author | Kim, Yeeun Choi, Changhoon Park, Jee Hyun Ahn, Won-Gyun Shin, Sung-Won Kim, Shin-Yeong Noh, Jae Myoung |
author_facet | Kim, Yeeun Choi, Changhoon Park, Jee Hyun Ahn, Won-Gyun Shin, Sung-Won Kim, Shin-Yeong Noh, Jae Myoung |
author_sort | Kim, Yeeun |
collection | PubMed |
description | PURPOSE: This study aims to investigate the effect of splenectomy on radiation-mediated growth inhibition and immune modulation in lung cancer xenograft models. MATERIALS AND METHODS: Human non-small cell lung cancer H1299 cells and murine Lewis lung carcinoma LL/2-luc cells were injected into the right hind leg of BALB/c-nude mice and C57BL/6 mice, respectively. Splenectomy or sham operation was performed prior to tumor cell injection or before and after irradiation during tumor growth. Irradiation was delivered with 2–3 fractions of 6 Gy X-ray using a linear accelerator. Flow cytometry analysis was performed for immune cell profiling. RESULTS: Splenectomy prior to tumor injection or at early stage inhibited growth of LL/2-luc tumors but not that of H1299 tumors; however, it did not enhance the antitumor effect of radiation regardless of intervention timing. Flow cytometry analysis showed monocytic myeloid-derived suppressor cells (MDSCs) and activated CD8(+) T cells increased after irradiation in the tumors of splenectomized mice, compared to those of sham-operated mice. Administration of anti-PD-1 (programmed death-1) antibodies improved the ability of splenectomy to attenuate the growth of irradiated tumors. CONCLUSION: Splenectomy has paradoxical effects on radiation-induced tumor growth inhibition, depending on tumor types and intervention timing, but it has an immune-modulating effect when combined with radiation. |
format | Online Article Text |
id | pubmed-8984136 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The Korean Society for Radiation Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-89841362022-04-13 Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy Kim, Yeeun Choi, Changhoon Park, Jee Hyun Ahn, Won-Gyun Shin, Sung-Won Kim, Shin-Yeong Noh, Jae Myoung Radiat Oncol J Original Article PURPOSE: This study aims to investigate the effect of splenectomy on radiation-mediated growth inhibition and immune modulation in lung cancer xenograft models. MATERIALS AND METHODS: Human non-small cell lung cancer H1299 cells and murine Lewis lung carcinoma LL/2-luc cells were injected into the right hind leg of BALB/c-nude mice and C57BL/6 mice, respectively. Splenectomy or sham operation was performed prior to tumor cell injection or before and after irradiation during tumor growth. Irradiation was delivered with 2–3 fractions of 6 Gy X-ray using a linear accelerator. Flow cytometry analysis was performed for immune cell profiling. RESULTS: Splenectomy prior to tumor injection or at early stage inhibited growth of LL/2-luc tumors but not that of H1299 tumors; however, it did not enhance the antitumor effect of radiation regardless of intervention timing. Flow cytometry analysis showed monocytic myeloid-derived suppressor cells (MDSCs) and activated CD8(+) T cells increased after irradiation in the tumors of splenectomized mice, compared to those of sham-operated mice. Administration of anti-PD-1 (programmed death-1) antibodies improved the ability of splenectomy to attenuate the growth of irradiated tumors. CONCLUSION: Splenectomy has paradoxical effects on radiation-induced tumor growth inhibition, depending on tumor types and intervention timing, but it has an immune-modulating effect when combined with radiation. The Korean Society for Radiation Oncology 2022-03 2022-02-23 /pmc/articles/PMC8984136/ /pubmed/35368201 http://dx.doi.org/10.3857/roj.2021.00885 Text en Copyright © 2022 The Korean Society for Radiation Oncology https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Kim, Yeeun Choi, Changhoon Park, Jee Hyun Ahn, Won-Gyun Shin, Sung-Won Kim, Shin-Yeong Noh, Jae Myoung Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
title | Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
title_full | Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
title_fullStr | Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
title_full_unstemmed | Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
title_short | Immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
title_sort | immunomodulatory effect of splenectomy in lung cancer mouse xenograft models receiving radiation therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8984136/ https://www.ncbi.nlm.nih.gov/pubmed/35368201 http://dx.doi.org/10.3857/roj.2021.00885 |
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