Evidence map›Paper›PMID 37880243›Full record

ArticleNature communications2023

IDH1 mutation impairs antiviral response and potentiates oncolytic virotherapy in glioma.

Xueqin Chen, Jun Liu, Yuqin Li, Yuequan Zeng, Fang Wang, Zexiong Cheng, Hao Duan, Guopeng Pan, Shangqi Yang, Yuling Chen and 15 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

23 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Precision virotherapy for IDH-mutant astrocytoma.Molecular therapy. Oncology · 2026
    Article
  3. Article
  4. Article
  5. Current medicinal chemistry · 2026
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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

25 authors at 4 institutions in 1 country.

Xueqin Chen *Department of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Jun Liu *Department of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.ORCID http://orcid.org/0000-0002-8563-7603
Yuqin Li *Department of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Yuequan ZengDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Fang WangDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Zexiong ChengDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Hao DuanDepartment of Neurosurgery/Neuro-oncology, State Key Laboratory of Oncology in South China, Sun Yat-sen University Cancer Center, 510060, Guangzhou, Guangdong, China.ORCID http://orcid.org/0000-0002-7078-8900
Guopeng PanDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Shangqi YangDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Yuling ChenDepartment of Pharmacology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, 200032, Shanghai, China.
Qing LiDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Xi ShenDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Ying LiDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Zixi QinDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Jiahong ChenDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Youwei HuangDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Xiangyu WangDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Yuli LuDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Minfeng ShuDepartment of Pharmacology, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, 200032, Shanghai, China.ORCID http://orcid.org/0000-0003-0514-1892
Yubo ZhangDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China.
Guocai WangInstitute of Traditional Chinese Medicine & Natural Products, Guangdong Province Key Laboratory of Pharmacodynamic Constituents of TCM and New Drugs Research, College of Pharmacy, Jinan University, 510632, Guangzhou, Guangdong, China.
Kai LiGuangdong Research Institute of Gastroenterology, The Sixth Affiliated Hospital of Sun Yat-sen University, 510655, Guangzhou, Guangdong, China.
Xi LinDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China. jnu_linxi@hotmail.com.
Fan XingMedical Research Institute, Guangdong Provincial People's Hospital (Guangdong Academy of Medical Sciences), Southern Medical University, 510080, Guangzhou, Guangdong, China. xingfan@gdph.org.cn.
Haipeng ZhangDepartment of Pharmacology, School of Medicine, Jinan University, 510632, Guangzhou, Guangdong, China. zhanghp@jnu.edu.cn.ORCID http://orcid.org/0000-0001-9188-542X
Jinan University · CNShanghai Medical College of Fudan University · CNSun Yat-sen University · CNGuangdong Academy of Medical Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IDH1 mutations frequently occur early in human glioma. While IDH1 mutation has been shown to promote gliomagenesis via DNA and histone methylation, little is known regarding its regulation in antiviral immunity. Here, we discover that IDH1 mutation inhibits virus-induced interferon (IFN) antiviral responses in glioma cells. Mechanistically, D2HG produced by mutant IDH1 enhances the binding of DNMT1 to IRF3/7 promoters such that IRF3/7 are downregulated, leading to impaired type I IFN response in glioma cells, which enhances the susceptibility of gliomas to viral infection. Furthermore, we identify DNMT1 as a potential biomarker predicting which IDH1mut gliomas are most likely to respond to oncolytic virus. Finally, both D2HG and ectopic mutant IDH1 can potentiate the replication and oncolytic efficacy of VSVΔ51 in female mouse models. These findings reveal a pivotal role for IDH1 mutation in regulating antiviral response and demonstrate that IDH1 mutation confers sensitivity to oncolytic virotherapy.

Indexed as

Brain NeoplasmsGliomaOncolytic VirotherapyOncolytic VirusesAnimalsFemaleHumansIsocitrate DehydrogenaseMethylationMiceMutationIDH1 protein, humanIdh1 protein, mouseIsocitrate Dehydrogenase

Identifiers

PMID37880243
PMCPMC10600173
OpenAlexW4387937014

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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 OpenQuestion graph.