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Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis
OBJECTIVE: To analyze the effect of carbon ion ((12)C(6+)) radiation may induce bystander effect on A549 cell metastasis and metabonomics. METHODS: A549 cell was irradiated with carbon ion to establish the clone survival model and the transwell matrix assay was applied to measure the effect of carbo...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962605/ https://www.ncbi.nlm.nih.gov/pubmed/33738244 http://dx.doi.org/10.3389/fonc.2020.601620 |
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author | Yang, Zhen Zhang, Qiuning Luo, Hongtao Shao, Lihua Liu, Ruifeng Kong, Yarong Zhao, Xueshan Geng, Yichao Li, Chengcheng Wang, Xiaohu |
author_facet | Yang, Zhen Zhang, Qiuning Luo, Hongtao Shao, Lihua Liu, Ruifeng Kong, Yarong Zhao, Xueshan Geng, Yichao Li, Chengcheng Wang, Xiaohu |
author_sort | Yang, Zhen |
collection | PubMed |
description | OBJECTIVE: To analyze the effect of carbon ion ((12)C(6+)) radiation may induce bystander effect on A549 cell metastasis and metabonomics. METHODS: A549 cell was irradiated with carbon ion to establish the clone survival model and the transwell matrix assay was applied to measure the effect of carbon ion on cell viability, migration, and invasion, respectively. Normal human embryonic lung fibroblasts (WI-38) were irradiated with carbon ions of 0 and 2 Gy and then transferred to A549 cell co-culture medium for 24 h. The migration and invasion of A549 cells were detected by the Transwell chamber. The analysis of metabonomic information in transfer medium by liquid phase mass spectrometry (LC-MS), The differential molecules were obtained by principal pomponent analysis (PCA) and the target proteins of significant differences (p = 1.7 × 10(−3)) obtained by combining with the STICH database. KEGG pathway was used to analyze the enrichment of the target protein pathway. RESULTS: Compared with 0 Gy, the colony formation, migration, and invasion of A549 cells were significantly inhibited by carbon ion 2 and 4 Gy irradiation, while the inhibitory effect was not significant after 1 Gy irradiation. Compared with 0 Gy, the culture medium 24 h after carbon ion 2 Gy irradiation significantly inhibited the metastasis of tumor cells (p = 0.03). LC-MS analysis showed that 23 differential metabolites were obtained in the cell culture medium 24 h after carbon ion 0 and 2 Gy irradiation (9 up-regulated and 14 down-regulated). Among them, two were up-regulated and two down-regulated (p = 2.9 × 10(−3)). 41 target proteins were corresponding to these four differential molecules. Through the analysis of the KEGG signal pathway, it was found that these target molecules were mainly enriched in purine metabolism, tyrosine metabolism, cysteine and methionine metabolism, peroxisome, and carbon metabolism. Neuroactive ligand-receptor interaction, calcium signaling pathway, arachidonic acid metabolism, and Fc epsilon RI signaling pathway. CONCLUSION: The bystander effect induced by 2 Gy carbon ion radiation inhibits the metastasis of tumor cells, which indicates that carbon ions may change the metabolites of irradiated cells, so that it may indirectly affect the metabolism of tumor cell growth microenvironment, thus inhibiting the metastasis of malignant tumor cells. |
format | Online Article Text |
id | pubmed-7962605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-79626052021-03-17 Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis Yang, Zhen Zhang, Qiuning Luo, Hongtao Shao, Lihua Liu, Ruifeng Kong, Yarong Zhao, Xueshan Geng, Yichao Li, Chengcheng Wang, Xiaohu Front Oncol Oncology OBJECTIVE: To analyze the effect of carbon ion ((12)C(6+)) radiation may induce bystander effect on A549 cell metastasis and metabonomics. METHODS: A549 cell was irradiated with carbon ion to establish the clone survival model and the transwell matrix assay was applied to measure the effect of carbon ion on cell viability, migration, and invasion, respectively. Normal human embryonic lung fibroblasts (WI-38) were irradiated with carbon ions of 0 and 2 Gy and then transferred to A549 cell co-culture medium for 24 h. The migration and invasion of A549 cells were detected by the Transwell chamber. The analysis of metabonomic information in transfer medium by liquid phase mass spectrometry (LC-MS), The differential molecules were obtained by principal pomponent analysis (PCA) and the target proteins of significant differences (p = 1.7 × 10(−3)) obtained by combining with the STICH database. KEGG pathway was used to analyze the enrichment of the target protein pathway. RESULTS: Compared with 0 Gy, the colony formation, migration, and invasion of A549 cells were significantly inhibited by carbon ion 2 and 4 Gy irradiation, while the inhibitory effect was not significant after 1 Gy irradiation. Compared with 0 Gy, the culture medium 24 h after carbon ion 2 Gy irradiation significantly inhibited the metastasis of tumor cells (p = 0.03). LC-MS analysis showed that 23 differential metabolites were obtained in the cell culture medium 24 h after carbon ion 0 and 2 Gy irradiation (9 up-regulated and 14 down-regulated). Among them, two were up-regulated and two down-regulated (p = 2.9 × 10(−3)). 41 target proteins were corresponding to these four differential molecules. Through the analysis of the KEGG signal pathway, it was found that these target molecules were mainly enriched in purine metabolism, tyrosine metabolism, cysteine and methionine metabolism, peroxisome, and carbon metabolism. Neuroactive ligand-receptor interaction, calcium signaling pathway, arachidonic acid metabolism, and Fc epsilon RI signaling pathway. CONCLUSION: The bystander effect induced by 2 Gy carbon ion radiation inhibits the metastasis of tumor cells, which indicates that carbon ions may change the metabolites of irradiated cells, so that it may indirectly affect the metabolism of tumor cell growth microenvironment, thus inhibiting the metastasis of malignant tumor cells. Frontiers Media S.A. 2021-03-02 /pmc/articles/PMC7962605/ /pubmed/33738244 http://dx.doi.org/10.3389/fonc.2020.601620 Text en Copyright © 2021 Yang, Zhang, Luo, Shao, Liu, Kong, Zhao, Geng, Li and Wang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Yang, Zhen Zhang, Qiuning Luo, Hongtao Shao, Lihua Liu, Ruifeng Kong, Yarong Zhao, Xueshan Geng, Yichao Li, Chengcheng Wang, Xiaohu Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis |
title | Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis |
title_full | Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis |
title_fullStr | Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis |
title_full_unstemmed | Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis |
title_short | Effect of Carbon Ion Radiation Induces Bystander Effect on Metastasis of A549 Cells and Metabonomic Correlation Analysis |
title_sort | effect of carbon ion radiation induces bystander effect on metastasis of a549 cells and metabonomic correlation analysis |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7962605/ https://www.ncbi.nlm.nih.gov/pubmed/33738244 http://dx.doi.org/10.3389/fonc.2020.601620 |
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