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Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways

Malignant Glioma is characterized by strong self-renewal potential and immature differentiation potential. The main reason is that malignant glioma holds key cluster cells, glioma stem cells (GSCs). GSCs contribute to tumorigenesis, tumor progression, recurrence, and treatment resistance. Interferon...

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Autores principales: Han, Xin-Xin, Jin, Shengkai, Yu, Li-Ming, Wang, Min, Hu, Xin-Yu, Hu, Dai-Yu, Ren, Jie, Zhang, Meng-Han, Huang, Wei, Deng, Jia-Jia, Chen, Qing-Qing, Gao, Zhengliang, He, Hua, Cai, Chunhui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Nature Singapore 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249963/
https://www.ncbi.nlm.nih.gov/pubmed/35778531
http://dx.doi.org/10.1186/s13619-022-00123-w
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author Han, Xin-Xin
Jin, Shengkai
Yu, Li-Ming
Wang, Min
Hu, Xin-Yu
Hu, Dai-Yu
Ren, Jie
Zhang, Meng-Han
Huang, Wei
Deng, Jia-Jia
Chen, Qing-Qing
Gao, Zhengliang
He, Hua
Cai, Chunhui
author_facet Han, Xin-Xin
Jin, Shengkai
Yu, Li-Ming
Wang, Min
Hu, Xin-Yu
Hu, Dai-Yu
Ren, Jie
Zhang, Meng-Han
Huang, Wei
Deng, Jia-Jia
Chen, Qing-Qing
Gao, Zhengliang
He, Hua
Cai, Chunhui
author_sort Han, Xin-Xin
collection PubMed
description Malignant Glioma is characterized by strong self-renewal potential and immature differentiation potential. The main reason is that malignant glioma holds key cluster cells, glioma stem cells (GSCs). GSCs contribute to tumorigenesis, tumor progression, recurrence, and treatment resistance. Interferon-beta (IFN-β) is well known for its anti-proliferative efficacy in diverse cancers. IFN-β also displayed potent antitumor effects in malignant glioma. IFN-β affect both GSCs and Neural stem cells (NSCs) in the treatment of gliomas. However, the functional comparison, similar or different effects of IFN-β on GSCs and NSCs are rarely reported. Here, we studied the similarities and differences of the responses to IFN-β between human GSCs and normal NSCs. We found that IFN-β preferentially inhibited GSCs over NSCs. The cell body and nucleus size of GSCs increased after IFN-β treatment, and the genomic analysis revealed the enrichment of the upregulated immune response, cell adhesion genes and down regulated cell cycle, ribosome pathways. Several typical cyclin genes, including cyclin A2 (CCNA2), cyclin B1 (CCNB1), cyclin B2 (CCNB2), and cyclin D1 (CCND1), were significantly downregulated in GSCs after IFN-β stimulation. We also found that continuous IFN-β stimulation after passage further enhanced the inhibitory effect. Our study revealed how genetic diversity resulted in differential effects in response to IFN-β treatment. These results may contribute to improve the applications of IFN-β in anti-cancer immunotherapy. In addition, these results may also help to design more effective pharmacological strategies to target cancer stem cells while protecting normal neural stem cells.
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spelling pubmed-92499632022-08-02 Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways Han, Xin-Xin Jin, Shengkai Yu, Li-Ming Wang, Min Hu, Xin-Yu Hu, Dai-Yu Ren, Jie Zhang, Meng-Han Huang, Wei Deng, Jia-Jia Chen, Qing-Qing Gao, Zhengliang He, Hua Cai, Chunhui Cell Regen Research Article Malignant Glioma is characterized by strong self-renewal potential and immature differentiation potential. The main reason is that malignant glioma holds key cluster cells, glioma stem cells (GSCs). GSCs contribute to tumorigenesis, tumor progression, recurrence, and treatment resistance. Interferon-beta (IFN-β) is well known for its anti-proliferative efficacy in diverse cancers. IFN-β also displayed potent antitumor effects in malignant glioma. IFN-β affect both GSCs and Neural stem cells (NSCs) in the treatment of gliomas. However, the functional comparison, similar or different effects of IFN-β on GSCs and NSCs are rarely reported. Here, we studied the similarities and differences of the responses to IFN-β between human GSCs and normal NSCs. We found that IFN-β preferentially inhibited GSCs over NSCs. The cell body and nucleus size of GSCs increased after IFN-β treatment, and the genomic analysis revealed the enrichment of the upregulated immune response, cell adhesion genes and down regulated cell cycle, ribosome pathways. Several typical cyclin genes, including cyclin A2 (CCNA2), cyclin B1 (CCNB1), cyclin B2 (CCNB2), and cyclin D1 (CCND1), were significantly downregulated in GSCs after IFN-β stimulation. We also found that continuous IFN-β stimulation after passage further enhanced the inhibitory effect. Our study revealed how genetic diversity resulted in differential effects in response to IFN-β treatment. These results may contribute to improve the applications of IFN-β in anti-cancer immunotherapy. In addition, these results may also help to design more effective pharmacological strategies to target cancer stem cells while protecting normal neural stem cells. Springer Nature Singapore 2022-07-02 /pmc/articles/PMC9249963/ /pubmed/35778531 http://dx.doi.org/10.1186/s13619-022-00123-w Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Han, Xin-Xin
Jin, Shengkai
Yu, Li-Ming
Wang, Min
Hu, Xin-Yu
Hu, Dai-Yu
Ren, Jie
Zhang, Meng-Han
Huang, Wei
Deng, Jia-Jia
Chen, Qing-Qing
Gao, Zhengliang
He, Hua
Cai, Chunhui
Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
title Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
title_full Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
title_fullStr Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
title_full_unstemmed Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
title_short Interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
title_sort interferon-beta inhibits human glioma stem cell growth by modulating immune response and cell cycle related signaling pathways
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9249963/
https://www.ncbi.nlm.nih.gov/pubmed/35778531
http://dx.doi.org/10.1186/s13619-022-00123-w
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