Evidence map›Paper›PMID 42904239›Full record

ArticleInternational journal of nanomedicine2026

Developing a Better Hepatocellular Carcinoma Treatment: AlEu MOF Nanoparticles Enhance Microwave Thermal Ablation and Synergistically Activate the cGAS-STING Pathway.

Shaoshi Ma, Yingying Wei, Borui Ma, Wenhui Dong, Feng Li, Xiao Li, Lin Chen, Yongzhen Yang, Shiping Yu

Abstract read
In one paragraph

Article in International journal of nanomedicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

9 authors.

Shaoshi Ma *Department of Interventional Therapy, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030013, People's Republic of China.
Yingying Wei *Department of Interventional Therapy, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030013, People's Republic of China.
Borui MaDepartment of Interventional Therapy, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030013, People's Republic of China.
Wenhui DongDepartment of Interventional Therapy, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030013, People's Republic of China.
Feng LiCentral Laboratory, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital/Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030013, People's Republic of China.ORCID 0000-0002-7935-0892
Xiao LiDepartment of Interventional Therapy, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, 100021, People's Republic of China.
Lin ChenKey Laboratory of Interface Science and Engineering in Advanced Materials, Ministry of Education, Taiyuan University of Technology, Taiyuan, Shanxi, 030024, People's Republic of China.
Yongzhen YangKey Laboratory of Interface Science and Engineering in Advanced Materials, Ministry of Education, Taiyuan University of Technology, Taiyuan, Shanxi, 030024, People's Republic of China.
Shiping YuDepartment of Interventional Therapy, Shanxi Province Cancer Hospital/Shanxi Hospital Affiliated to Cancer Hospital, Chinese Academy of Medical Sciences/Cancer Hospital Affiliated to Shanxi Medical University, Taiyuan, Shanxi, 030013, People's Republic of China.ORCID 0000-0002-1783-1674

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To address the high recurrence rate of hepatocellular carcinoma (HCC) following microwave ablation (MWA) therapy, this study develops aluminum-europium metal-organic framework (AlEu MOF) nanoparticles that enhance MWA efficacy by physically improving thermal ablation and activating cyclic GMP-AMP (cGAMP) synthase-stimulator of interferon genes (cGAS-STING)-mediated antitumor immunity. Methods: AlEu MOF nanoparticles were synthesized via a one-pot hydrothermal method and characterized for physicochemical properties. Biocompatibility and in vitro cell-killing efficacy in combination with MWA were evaluated in Hepa1-6 cell lines. Immunostimulatory capacity was assessed by measuring activation markers of the cGAS-STING pathway. In vivo antitumor efficacy was investigated in a Hepa1-6 subcutaneous tumor-bearing mouse model, with monitoring of tumor growth, intratumoral temperature elevation, serum levels of cGAS-STING pathway downstream effectors, and treatment safety. Results: AlEu MOF nanoparticles demonstrated excellent biocompatibility and hemocompatibility. In combination with MWA, AlEu MOF significantly enhanced thermal efficiency within tumors, resulting in superior tumor growth inhibition compared with MWA alone. Mechanistically, the enhanced thermal ablation triggered mitochondrial damage and downstream cGAS-STING pathway activation, as evidenced by elevated serum levels of key downstream cytokines (IFN-γ, IL-6 and TNF-α) in the combination therapy group. No significant hepatorenal toxicity or major organ damage was observed throughout the treatment period. Conclusion: The AlEu MOF nanoparticles potentiate MWA therapy through a dual synergistic mechanism: enhanced thermal ablation serves as the upstream trigger for cGAS-STING activation, while europium ions simultaneously amplify the STING signaling output, together converting local thermal ablation into systemic antitumor immunity. This synergistic strategy offers a promising approach for enhancing both local tumor ablation and systemic antitumor immunity in HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMicrowavesNanoparticlesAnimalsCell Line, TumorcGAS-STING Signaling PathwayCombined Modality TherapyCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseHumansMaleMembrane ProteinsMiceNucleotidyltransferasesSignal TransductionSTING ProteinCyclic Guanosine Monophosphate-Adenosine Monophosphate SynthaseMembrane ProteinsNucleotidyltransferasesSting1 protein, mouseSTING ProteincGAS-STINGhepatocellular carcinomametal-organic frameworksmicrowave ablation

Identifiers

PMID42904239
PMCPMC13682527

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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.