Evidence map›Paper›PMID 40150864›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

IR783-Stabilized Nanodrugs Enhance Anticancer Immune Response by Synergizing Oxidation Therapy and Epigenetic Modulation.

Jinzhao Liu, Meicen Wu, Qingyang Lyu, Chang Yang, Ni Fan, Kang Chen, Weiping Wang

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Review
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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

7 authors.

Jinzhao LiuState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Meicen WuState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Qingyang LyuState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Chang YangState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Ni FanState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Kang ChenState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.
Weiping WangState Key Laboratory of Pharmaceutical Biotechnology, The University of Hong Kong, Hong Kong, China.ORCID https://orcid.org/0000-0001-7511-3497

Funding

National Natural Science Foundation of China 82222903
6 · The paper itself

Abstract

Immune evasion and metastasis are the leading causes of poor prognosis in triple-negative breast cancer treatment. Since current standard immunotherapies have limited efficacy due to immunologically cold microenvironment, it is crucial to explore new strategies to sensitize anticancer immune response. In this study, it is found that incorporating β-lapachone-based oxidation therapy with CUDC101-initiated epigenetic regulation results in synergistic antitumor effects and potent immune activation. To co-deliver these two hydrophobic drugs, IR783 with cyanine structure serves as the stabilizer to form a nanoformulation based on small molecule self-assembly. Such IR783-stabilized nanodrugs can not only lead to cancer cell apoptosis through HDAC inhibition-enhanced oxidation therapy but also cooperatively induce immunogenic cell death and promote pro-inflammatory cytokine gene expression to reshape immunosuppressive microenvironment. Besides, nanodrugs can inhibit both primary and distant tumor growth effectively by elevating systemic anticancer immunity. This study provides a promising approach to synergize oxidation therapy with epigenetic modulation for safe and efficient breast cancer immunotherapy.

Indexed as

Antineoplastic AgentsEpigenesis, GeneticTriple Negative Breast NeoplasmsAnimalsApoptosisCell Line, TumorFemaleHumansImmunotherapyMiceNanoparticlesOxidation-ReductionTumor MicroenvironmentAntineoplastic Agentscancer immunotherapyepigenetic regulationimmunogenic cell deathoxidation therapysmall molecule self‐assemblysynergistic effect

Identifiers

PMID40150864
PMCPMC12140360

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.