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Series GSE171041 Query DataSets for GSE171041
Status Public on Apr 28, 2021
Title 16s rDNA-sequencing of gut microbiota in Temozolomide-treated glioma mice
Organism mouse gut metagenome
Experiment type Other
Summary Purpose: Gut microbiota is associated with the progression of brain tumor. However, the alterations in the gut microbiota during glioma growth and temozolomide (TMZ) therapy remains to be understood.
Methods: C57BL/6 male mice were implanted with GL261 glioma cells. TMZ/sodium carboxymethyl cellulose (SCC) was administered by gavage for five consecutive days (from 8 to 12 days after implantation). Fecal samples were collected before (T0) and on days 7 (T1), 14 (T2), and 28 (T3) after implantation. The gut microbiota was analyzed using 16S ribosomal DNA sequencing followed by absolute and relative quantitation analyses.
Results: Nineteen genera were altered during glioma progression with the most dramatic changes in Firmicutes and Bacteroidetes phyla. During glioma growth, Lactobacillus abundance decreased at the earlier stage of glioma development (T1), and then gradually increased (T2, T3); Intestinimonas abundance exhibited a persistent increase; Anaerotruncus showed a transient increase and then a subsequent decrease. Twenty genera altered following TMZ treatment. The enrichment of Akkermansia and Bifidobacterium was observed only at the early stage following TMZ treatment (T2), but not at the later stage (T3). Additionally, the decrease of Anaerotruncus was slighter in TMZ group at T3 comparing to the vehicle group. The abundance of Intestinimonas increased constantly during the progression of glioma, but was unaffected by TMZ.
Conclusions: Glioma development and progression resulted in altered gut microbiota. TMZ reversed the decrease of Anaerotruncus in glioma at T3, and increased the abundance of Bifidobacterium with no influence on the increase of Intestinimonas. Short-term and long-term effects of TMZ treatment on the bacterial communities may be differential. This study will improve understanding the role of gut microbiota in glioma, and help develop gut microbiota as a potential therapeutic target.
 
Overall design 16s rDNA-sequencing was performed on 48 samples to detect gut microbiota change during glioma progression and the effect of Temozolomide on gut microbiota in glioma mice.
 
Contributor(s) Li X, Wu B, Jiang Y, Li J, Wang Z, Ma C, Li Y, Yao J, Jin X, Li Z
Citation https://doi.org/10.2147/DDDT.S298261
Submission date Mar 29, 2021
Last update date Apr 28, 2021
Contact name Zhi-Qiang Li
E-mail(s) [email protected]
Phone 0086 18907123005
Organization name Zhongnan Hospital of Wuhan university
Department neurosurgery
Street address No.169 Donghu road
City Wuhan
State/province Hubie
ZIP/Postal code 430071
Country China
 
Platforms (1)
GPL22735 Illumina HiSeq 2500 (mouse gut metagenome)
Samples (48)
GSM5217230 TMZ group, 01_01
GSM5217231 TMZ group, 01_02
GSM5217232 TMZ group, 01_03
Relations
BioProject PRJNA718207
SRA SRP312566

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Supplementary file Size Download File type/resource
GSE171041_absolute_quantification_otu_table.txt.gz 92.5 Kb (ftp)(http) TXT
GSE171041_relative_quantification_otu_table.xls.gz 122.0 Kb (ftp)(http) XLS
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Raw data are available in SRA
Processed data are available on Series record

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