Evidence map›Paper›PMID 36927689›Full record

ArticleJournal of translational medicine2023

Gut microbiota mediated the individualized efficacy of Temozolomide via immunomodulation in glioma.

Xiaoying Hou, Hongzhi Du, Yufei Deng, Haiping Wang, Jinmi Liu, Jialu Qiao, Wei Liu, Xiji Shu, Binlian Sun, Yuchen Liu

Open access · goldFull text read
In one paragraph

Article in Journal of translational medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
7.1field-weighted citation impact, top 2% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

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  12. Interplay between the gut microbiota, its metabolites and carcinogens.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 1 country.

Xiaoying Hou *Wuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Hongzhi Du *School of Pharmacy, Hubei University of Chinese Medicine, Wuhan, China.
Yufei DengWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Haiping WangWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Jinmi LiuWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Jialu QiaoWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Wei LiuWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Xiji ShuWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China.
Binlian SunWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China. binlian17@jhun.edu.cn.
Yuchen LiuWuhan Institute of Biomedical Sciences, School of Medicine, Jianghan University, Wuhan, China. yuchen.liu@jhun.edu.cn.
Jianghan University · CNHubei University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTemozolomide (TMZ) is the preferred chemotherapy strategy for glioma therapy. As a second-generation alkylating agent, TMZ provides superior oral bio-availability. However, limited response rate (less than 50%) and high incidence of drug resistance seriously restricts TMZ's application, there still lack of strategies to increase the chemotherapy sensitivity.

methodsLuci-GL261 glioma orthotopic xenograft model combined bioluminescence imaging was utilized to evaluate the anti-tumor effect of TMZ and differentiate TMZ sensitive (S)/non-sensitive (NS) individuals. Integrated microbiomics and metabolomics analysis was applied to disentangle the involvement of gut bacteria in TMZ sensitivity. Spearman's correlation analysis was applied to test the association between fecal bacteria levels and pharmacodynamics indices. Antibiotics treatment combined TMZ treatment was used to confirm the involvement of gut microbiota in TMZ response. Flow cytometry analysis, ELISA and histopathology were used to explore the potential role of immunoregulation in gut microbiota mediated TMZ response.

resultsFirstly, gut bacteria composition was significantly altered during glioma development and TMZ treatment. Meanwhile, in vivo anti-cancer evaluation suggested a remarkable difference in chemotherapy efficacy after TMZ administration. Moreover, 16s rRNA gene sequencing and non-targeted metabolomics analysis revealed distinct different gut microbiota and immune infiltrating state between TMZ sensitive and non-sensitive mice, while abundance of differential gut bacteria and related metabolites was significantly correlated with TMZ pharmacodynamics indices. Further verification suggested that gut microbiota deletion by antibiotics treatment could accelerate glioma development, attenuate TMZ efficacy and inhibit immune cells (macrophage and CD8α

conclusionsThe current study confirmed the involvement of gut microbiota in glioma development and individualized TMZ efficacy via immunomodulation, hence gut bacteria may serve as a predictive biomarker as well as a therapeutic target for clinical TMZ application.

Indexed as

Brain NeoplasmsGastrointestinal MicrobiomeGliomaAnimalsAntineoplastic Agents, AlkylatingCell Line, TumorDrug Resistance, NeoplasmHumansImmunomodulationMiceRNA, Ribosomal, 16STemozolomideAntineoplastic Agents, AlkylatingRNA, Ribosomal, 16STemozolomideFecal microbiomeFunctional MetabolomicsGliomaIndividualized efficacyTemozolomide

Identifiers

PMID36927689
PMCPMC10018922
OpenAlexW4327684345

What Socratic holds

Textfull text, public
LicenceCC BY
reference markers read1
measurements read50
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.