Evidence map›Paper›PMID 38889339›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

Co-delivery Nano System of MS-275 and V-9302 Induces Pyroptosis and Enhances Anti-Tumor Immunity Against Uveal Melanoma.

Hong Ren, Zhenkai Wu, Jia Tan, Hui Tao, Wangyuan Zou, Zheng Cao, Binyu Wen, Ziyi Cai, Jiaqi Du, Zhihong Deng

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing 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

31 citing papers in PubMed.

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  19. Targeting glutamine metabolism as a potential target for cancer treatment.Journal of experimental & clinical cancer research : CR · 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.

Hong RenDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, China.
Zhenkai WuDepartment of Ophthalmology, Changde Hospital, Xiangya School of Medicine, Central South University, Changde, Hunan, 415000, China.
Jia TanEye Center of Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China.
Hui TaoDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, China.
Wangyuan ZouDepartment of Anesthesiology, Xiangya Hospital, Central South University, Changsha, Hunan, 410008, China.
Zheng CaoDepartment of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA, 90066, USA.
Binyu WenDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, China.
Ziyi CaiDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, China.
Jiaqi DuDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, China.
Zhihong DengDepartment of Ophthalmology, The Third Xiangya Hospital, Central South University, Changsha, Hunan, 410013, China.ORCID 0000-0001-9926-4943

Funding

National Natural Science Foundation of China 82071002National Natural Science Foundation of China 82271057Natural Science Foundation of Hunan Province 2019JJ40465
6 · The paper itself

Abstract

In the treatment of uveal melanoma (UVM), histone deacetylase inhibitors (HDACi) have emerged as a promising epigenetic therapy. However, their clinical efficacy is hindered by the suboptimal pharmacokinetics and the strong self-rescue of tumor cells. To overcome these limitations, reactive oxygen species (ROS)-responsive nanoparticles (NPs) are designed that encapsulate HDACi MS-275 and the glutamine metabolism inhibitor V-9302. Upon reaching the tumor microenvironment, these NPs can disintegrate, thereby releasing MS-275 to increase the level of ROS and V-9302 to reduce the production of glutathione (GSH) related to self-rescue. These synergistic effects lead to a lethal ROS storm and induce cell pyroptosis. When combined with programmed cell death protein 1 monoclonal antibodies (α-PD-1), these NPs facilitate immune cell infiltration, improving anti-tumor immunity, converting "immune-cold" tumors into "immune-hot" tumors, and enhancing immune memory in mice. The findings present a nano-delivery strategy for the co-delivery of epigenetic therapeutics and metabolic inhibitors, which induces pyroptosis in tumors cells and improves the effectiveness of chemotherapy and immunotherapy.

Indexed as

MelanomaNanoparticlesPyridinesPyroptosisUveal NeoplasmsAnimalsBenzamidesCell Line, TumorDisease Models, AnimalDrug Delivery SystemsHistone Deacetylase InhibitorsHumansMiceTumor MicroenvironmentUveal MelanomaBenzamidesentinostatHistone Deacetylase InhibitorsPyridinesepigenetic therapyimmunotherapymetabolic interventionpyroptosisuveal melanoma

Identifiers

PMID38889339
PMCPMC11336933

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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.