Evidence map›Paper›PMID 41388189›Full record

ArticleCell death and differentiation2026

Chemotherapy induces multiple sclerosis-like neuropathologies that can be rescued by clobetasol.

Qiuyun Yuan, Wanchun Yang, Siliang Chen, Yunbo Yuan, Jingwen Gong, Tengfei Li, Mingrong Zuo, Yuting Shu, Yuze He, Yue Qin and 5 more

Abstract read
In one paragraph

Article in Cell death and differentiation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

15 authors.

Qiuyun Yuan *Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Wanchun Yang *Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Siliang Chen *Department of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yunbo YuanDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Jingwen GongDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Tengfei LiDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Mingrong ZuoDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yuting ShuDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yuze HeDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yue QinDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
Zhihao WangDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China.
Xiaoqiang XiaDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yiyuan CuiDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China.
Yanhui LiuDepartment of Neurosurgery, West China Hospital, Sichuan University, Chengdu, 610041, China. liuyh@scu.edu.cn.ORCID http://orcid.org/0000-0002-3722-3334
Mina ChenDepartment of Biotherapy, Cancer Center and State Key Laboratory of Biotherapy, West China Hospital, Sichuan University, Chengdu, 610041, China. chenmina2010@scu.edu.cn.ORCID http://orcid.org/0000-0002-7446-3978

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81571195National Natural Science Foundation of China (National Science Foundation of China) 82272644National Natural Science Foundation of China (National Science Foundation of China) 82372836
6 · The paper itself

Abstract

Chemotherapy is essential for cancer management yet frequently accompanied with adverse effects, particularly for temozolomide (TMZ), a frontline chemotherapeutic agent for glioma. Although clinical neurological abnormalities linked to TMZ have been observed, mechanisms underlying TMZ-induced neural impairments remain poorly understood, and effective interventions are lacking. Here, we demonstrated that TMZ chemotherapy induced neurodegenerations that recapitulated pathological features of multiple sclerosis, including demyelination, neuroinflammation and axonal degeneration. In adolescent mice, TMZ treatment resulted in severe white matter damage that spontaneously recovered, whereas in adult mice, moderate myelin damage persisted without recovery within the same timeframe. Importantly, we identified that clobetasol effectively reversed TMZ-induced white matter damage and trends toward anxiety and depression in adult mice by suppressing TMZ-induced AMPK activation and attenuating neuroinflammation, thereby promoting remyelination. Our findings reveal the previously underappreciated neural toxicities associated with TMZ chemotherapy and highlight the therapeutic efficacy of clobetasol in mitigating chemotherapy-induced neural impairment, providing a strategy to enhance the life quality of cancer patients.

Indexed as

Antineoplastic Agents, AlkylatingClobetasolMultiple SclerosisTemozolomideAnimalsMaleMiceMice, Inbred C57BLMyelin SheathAntineoplastic Agents, AlkylatingClobetasolTemozolomide

Identifiers

PMID41388189
PMCPMC13247271

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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.