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Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c
Lycium barbarum polysaccharide (LBP) is a substance with various biological activities extracted from Lycium barbarum. LbGPs are peptidoglycans with a short peptide backbone and a complex, branched glycan moiety, which is further extracted and isolated from LBPs. Previous studies have shown that LbG...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group US
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425286/ https://www.ncbi.nlm.nih.gov/pubmed/37069338 http://dx.doi.org/10.1038/s41417-023-00611-4 |
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author | Yao, Jian Hui, Jian-wen Chen, Yan-jun Luo, Dong-yang Yan, Jiang-shu Zhang, Yi-fan Lan, Yuan-xiang Yan, Xiu-rui Wang, Zhi-hua Fan, Heng Xia, He-chun |
author_facet | Yao, Jian Hui, Jian-wen Chen, Yan-jun Luo, Dong-yang Yan, Jiang-shu Zhang, Yi-fan Lan, Yuan-xiang Yan, Xiu-rui Wang, Zhi-hua Fan, Heng Xia, He-chun |
author_sort | Yao, Jian |
collection | PubMed |
description | Lycium barbarum polysaccharide (LBP) is a substance with various biological activities extracted from Lycium barbarum. LbGPs are peptidoglycans with a short peptide backbone and a complex, branched glycan moiety, which is further extracted and isolated from LBPs. Previous studies have shown that LbGP can inhibit cancer cell growth, but its specific mechanism is not completely clear. In this study, we found that LbGP could inhibit the proliferation of glioma cells and promote the expression of period 2 (PER2) through the PKA-CREB pathway. In addition, LbGP could inhibit the de novo synthesis of lipids by downregulating SREBP1c and its target genes, which depended on the expression of PER2. Moreover, PER2 negatively regulated the expression of SREBP1c via suppressing PI3K/AKT/mTOR pathway. In summary, LbGP may upregulate the expression of PER2 to reduce the expression of SREBP1c, inhibit lipid synthesis in glioblastoma, and inhibit glioblastoma cell proliferation. This study provides an alternative drug for the treatment of glioma and elucidates its potential mechanism. |
format | Online Article Text |
id | pubmed-10425286 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group US |
record_format | MEDLINE/PubMed |
spelling | pubmed-104252862023-08-16 Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c Yao, Jian Hui, Jian-wen Chen, Yan-jun Luo, Dong-yang Yan, Jiang-shu Zhang, Yi-fan Lan, Yuan-xiang Yan, Xiu-rui Wang, Zhi-hua Fan, Heng Xia, He-chun Cancer Gene Ther Article Lycium barbarum polysaccharide (LBP) is a substance with various biological activities extracted from Lycium barbarum. LbGPs are peptidoglycans with a short peptide backbone and a complex, branched glycan moiety, which is further extracted and isolated from LBPs. Previous studies have shown that LbGP can inhibit cancer cell growth, but its specific mechanism is not completely clear. In this study, we found that LbGP could inhibit the proliferation of glioma cells and promote the expression of period 2 (PER2) through the PKA-CREB pathway. In addition, LbGP could inhibit the de novo synthesis of lipids by downregulating SREBP1c and its target genes, which depended on the expression of PER2. Moreover, PER2 negatively regulated the expression of SREBP1c via suppressing PI3K/AKT/mTOR pathway. In summary, LbGP may upregulate the expression of PER2 to reduce the expression of SREBP1c, inhibit lipid synthesis in glioblastoma, and inhibit glioblastoma cell proliferation. This study provides an alternative drug for the treatment of glioma and elucidates its potential mechanism. Nature Publishing Group US 2023-04-17 2023 /pmc/articles/PMC10425286/ /pubmed/37069338 http://dx.doi.org/10.1038/s41417-023-00611-4 Text en © The Author(s) 2023, corrected publication 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Yao, Jian Hui, Jian-wen Chen, Yan-jun Luo, Dong-yang Yan, Jiang-shu Zhang, Yi-fan Lan, Yuan-xiang Yan, Xiu-rui Wang, Zhi-hua Fan, Heng Xia, He-chun Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c |
title | Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c |
title_full | Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c |
title_fullStr | Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c |
title_full_unstemmed | Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c |
title_short | Lycium barbarum glycopeptide targets PER2 to inhibit lipogenesis in glioblastoma by downregulating SREBP1c |
title_sort | lycium barbarum glycopeptide targets per2 to inhibit lipogenesis in glioblastoma by downregulating srebp1c |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10425286/ https://www.ncbi.nlm.nih.gov/pubmed/37069338 http://dx.doi.org/10.1038/s41417-023-00611-4 |
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