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GEO help: Mouse over screen elements for information. |
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Status |
Public on Dec 07, 2021 |
Title |
Rutaecarpine inhibits glioblastoma migration by activating the aryl hydrocarbon receptor (AhR) signaling pathway |
Organism |
Homo sapiens |
Experiment type |
Expression profiling by high throughput sequencing
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Summary |
Glioblastoma is the most frequent and aggressive primary astrocytoma in adults. The high migration ability of the tumor cells is an important reason for the high recurrence rate and poor prognosis of glioblastoma. Recently, emerging evidence has shown that the migration ability of glioblastoma cell was inhibited upon the activation of aryl hydrocarbon receptor (AhR), suggesting potential anti-tumor effects of AhR agonists. Rutaecarpine is a natural compound with potential tumor therapeutic effects which can possibly bind to AhR. However, its effect on the migration of glioblastoma is unclear. Therefore, we aim to explore the effects of rutaecarpine on the migration of human glioblastoma cells U87 and the involvements of the AhR signaling pathway. The results showed that: (i) compared with other structural related alkaloids, like evodiamine and dehydroevodiamine, rutaecarpine was a more potent AhR activator, and has stronger inhibitory effect on the glioblastoma cell migration; (ii) rutaecarpine decreased the migration ability of U87 cells in an AhR-dependent manner; (iii) AhR mediated the expression of a tumor suppressor interleukin 24 (IL24) induced by rutaecarpine, and AhR-IL24 axis was involved in the anti-migratoryeffects of rutaecarpine on the glioblastoma. Besides IL24, other motility related genes were proposed to participate in the migration regulation process of rutaecarpine by RNA-Seq analysis. These data suggest that rutaecarpine is a natural AhR agonist that could inhibit the migration of glioblastomaandbe a potential candidate for developing therapeutic drug against glioblatoma.
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Overall design |
Human glioblastoma cell line U87 mRNA profiles exposed to 10^-4 M rutaecarpin for 48 hours
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Contributor(s) |
Liu Y, Chen Y, Zhu R, Xu L, Xie HQ, Zhao B |
Citation(s) |
34955744 |
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Submission date |
Sep 07, 2021 |
Last update date |
Jan 10, 2022 |
Contact name |
Yiyun Liu |
E-mail(s) |
yschen@rcees.ac.cn
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Organization name |
Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences
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Street address |
18 Shuangqing Road, Haidian District, Beijing
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City |
Beijing |
ZIP/Postal code |
100085 |
Country |
China |
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Platforms (1) |
GPL24676 |
Illumina NovaSeq 6000 (Homo sapiens) |
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Samples (6)
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Relations |
BioProject |
PRJNA761394 |
SRA |
SRP336034 |
Supplementary file |
Size |
Download |
File type/resource |
GSE183606_differentially_expressed_genes.xls.gz |
126.1 Kb |
(ftp)(http) |
XLS |
GSE183606_gene_expression.txt.gz |
957.0 Kb |
(ftp)(http) |
TXT |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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