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CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation
The rise in population aging worldwide is causing an unparalleled increase in death from many cancers, including glioblastoma (GBM). In advanced countries, the number of elderly people living alone is increasing due to the rapid aging of the population and the socialization of nuclear families. Here...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699091/ http://dx.doi.org/10.1093/noajnl/vdaa143.013 |
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author | Yamashita, Daisuke Flanary, Victoria Yamaguchi, Shinobu Ohtsuka, Yoshihiro Ozaki, Saya Suehiro, Satoshi Inoue, Akihiro Gorospe, Myriam Nakano, Ichiro Kunieda, Takeharu |
author_facet | Yamashita, Daisuke Flanary, Victoria Yamaguchi, Shinobu Ohtsuka, Yoshihiro Ozaki, Saya Suehiro, Satoshi Inoue, Akihiro Gorospe, Myriam Nakano, Ichiro Kunieda, Takeharu |
author_sort | Yamashita, Daisuke |
collection | PubMed |
description | The rise in population aging worldwide is causing an unparalleled increase in death from many cancers, including glioblastoma (GBM). In advanced countries, the number of elderly people living alone is increasing due to the rapid aging of the population and the socialization of nuclear families. Here, we explored the impact of aging and social isolation on GBM tumorigenesis. In normal brain tissue, aging promoted pathways related to cytokines and inflammation, which were further promoted by social isolation. In tumor tissues, the expression of neuron/synapse-related genes was significantly reduced in aged mice, and their expression was further reduced by social isolation. In addition, the survival period of aged mice was significantly shorter than that of young mice, and the survival period was further shortened by social isolation, which was characteristic of males. This phenomenon was the same in humans, and the survival period in the young group was significantly longer than that in the elderly group, and in the elderly group, the survival period was shortened in the male elderly group living alone. Our data indicate that social isolation contributes to the highly aggressive GBM by the shift to neuro-inflammation in the elderly brain. |
format | Online Article Text |
id | pubmed-7699091 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-76990912020-12-02 CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation Yamashita, Daisuke Flanary, Victoria Yamaguchi, Shinobu Ohtsuka, Yoshihiro Ozaki, Saya Suehiro, Satoshi Inoue, Akihiro Gorospe, Myriam Nakano, Ichiro Kunieda, Takeharu Neurooncol Adv Supplement Abstracts The rise in population aging worldwide is causing an unparalleled increase in death from many cancers, including glioblastoma (GBM). In advanced countries, the number of elderly people living alone is increasing due to the rapid aging of the population and the socialization of nuclear families. Here, we explored the impact of aging and social isolation on GBM tumorigenesis. In normal brain tissue, aging promoted pathways related to cytokines and inflammation, which were further promoted by social isolation. In tumor tissues, the expression of neuron/synapse-related genes was significantly reduced in aged mice, and their expression was further reduced by social isolation. In addition, the survival period of aged mice was significantly shorter than that of young mice, and the survival period was further shortened by social isolation, which was characteristic of males. This phenomenon was the same in humans, and the survival period in the young group was significantly longer than that in the elderly group, and in the elderly group, the survival period was shortened in the male elderly group living alone. Our data indicate that social isolation contributes to the highly aggressive GBM by the shift to neuro-inflammation in the elderly brain. Oxford University Press 2020-11-28 /pmc/articles/PMC7699091/ http://dx.doi.org/10.1093/noajnl/vdaa143.013 Text en © The Author(s) 2020. Published by Oxford University Press, the Society for Neuro-Oncology and the European Association of Neuro-Oncology. http://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/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Supplement Abstracts Yamashita, Daisuke Flanary, Victoria Yamaguchi, Shinobu Ohtsuka, Yoshihiro Ozaki, Saya Suehiro, Satoshi Inoue, Akihiro Gorospe, Myriam Nakano, Ichiro Kunieda, Takeharu CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation |
title | CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation |
title_full | CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation |
title_fullStr | CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation |
title_full_unstemmed | CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation |
title_short | CBMS-01 Mechanism of brain tumor malignancy caused by aging and social isolation |
title_sort | cbms-01 mechanism of brain tumor malignancy caused by aging and social isolation |
topic | Supplement Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7699091/ http://dx.doi.org/10.1093/noajnl/vdaa143.013 |
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