Evidence map›Paper›PMID 42839637›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2026

Inhibition of MEKK3 Prevents Cerebral Cavernous Malformation Progression Via Restoring Endothelial Integrity and Restricting Microglial Activation.

Weiwei Zheng, Suyun Yu, Liwenyu Chen, Jing Ma, Peiliang Shen, Chang Yu, Xiaoqing Xin, Qiuhong Shen, Jing Chen, Song Ke and 8 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 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

18 authors.

Weiwei Zheng *Jiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Suyun Yu *Jiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0001-7898-8141
Liwenyu ChenJiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Jing MaJiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Peiliang ShenDepartment of Biochemistry and Molecular Biology, School of Medicine, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0009-0003-2281-2894
Chang YuJiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.
Xiaoqing XinDepartment of Biochemistry and Molecular Biology, School of Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Qiuhong ShenDepartment of Biochemistry and Molecular Biology, School of Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Jing ChenDepartment of Biochemistry and Molecular Biology, School of Medicine, Nanjing University of Chinese Medicine, Nanjing, China.
Song KeMatwings Technology Company, Shanghai, China.
Hao LiuMatwings Technology Company, Shanghai, China.
Xiaobing JiangState Key Laboratory of Oncology in South China, Collaborative Innovation Center for Cancer Medicine, Department of Neurosurgery, Sun Yat-sen University Cancer Center, Guangzhou, China.ORCID https://orcid.org/0000-0001-6566-7269
Ruogu QiDepartment of Biochemistry and Molecular Biology, School of Medicine, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0001-9222-9272
Juming YanJiangsu Key Laboratory of Immunity and Metabolism, Department of Pathogenic Biology and Immunology, National Experimental Demonstration Center for Basic Medicine Education, Xuzhou Laboratory of Infection and Immunity, Xuzhou Medical University, Xuzhou, China.
Jia LiCurtin Medical Research Institute and Curtin Medical School, Curtin University, Bentley, WA, Australia.
Jaesung P ChoiSchool of Biomedical Sciences, University of New South Wales, Sydney, NSW, Australia.
Yin LuJiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0003-2063-8485
Yang ZhaoJiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica, Nanjing University of Chinese Medicine, Nanjing, China.ORCID https://orcid.org/0000-0001-8814-7004

Funding

China Postdoctoral Science Foundation 2025M783888China Postdoctoral Science Foundation GZC20262146Innovation Project of Jiangsu Key Laboratory for Pharmacology and Safety Research of Chinese Materia Medica 2026JKLPSRCMM12Innovation Project of SKL of Technologies for Chinese Medicine Pharmaceutical Process Control and Intelligent Manufacture NZYSKL2601Key Program of Natural Science Foundation for Jiangsu Higher Education Institutions 22KJA360007National Key Research and Development Program of China 2025YFC3507500National Natural Science Foundation of China 82274233National Natural Science Foundation of China 82574731National Natural Science Foundation of China 82608254Natural Science Foundation of Jiangsu Province BK20240146Noncommunicable Chromic Diseases- National Science and Technology Major Project 2024ZD0530800Science and Technology Development Fund 0003/2025/NRP
6 · The paper itself

Abstract

Cerebral cavernous malformations (CCMs) are characterized by aberrant MEKK3 activation, yet how MEKK3 governs lesion maturation and whether it represents a viable therapeutic target remain unclear. We demonstrate that endothelial MEKK3 initiates lesion formation, whereas microglial MEKK3 exacerbates late-stage progression. Mechanistically, MEKK3 activation in endothelial cells disrupts junctional integrity and promotes fibrinogen leakage; fibrinogen-recruited microglia subsequently amplify vascular injury via MEKK3-NF-κB-dependent uptake of damaged endothelial debris. Through AI-assisted drug design and structural optimization, we identified (R)-1,6-dimethyl-11-phenyl-1,10-dihydro-2H-furo[2',3':1,2]phenanthrol[3,4-d]imidazole (DPDH) as a potent MEKK3 inhibitor. DPDH suppresses MEKK3-KLF2/4 signaling in endothelial cells to restore barrier integrity and inhibits MEKK3-NF-κB in microglia to restrain their activation and uptake of damaged endothelial cells. Collectively, our findings establish that MEKK3 signaling in both endothelial cells and microglia drives CCM progression, and position DPDH as a promising therapeutic candidate for CCM treatment.

Indexed as

cerebral cavernous malformationDPDHendothelial cellsfibrinogenMEKK3microglial cells

Identifiers

PMID42839637
PMCPMC13643112

What OpenQuestion holds

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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.