Evidence map›Paper›PMID 41765880›Full record

ArticleJournal of nanobiotechnology2026

Ultrasound and ROS-responsive nanodroplets inhibit TCA cycle in hepatocellular carcinoma.

Ting Zhao, Lu Guo, Ning Cong, Yading Zhao, Xiaoxuan Wang, Xinyu Zeng, Suyun Li, Rui Liu, Shuting Huang, Yuye Fu and 1 more

Abstract read
In one paragraph

Article in Journal of nanobiotechnology, 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

11 authors.

Ting Zhao *Department of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Lu Guo *Department of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Ning Cong *Department of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Yading ZhaoDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Xiaoxuan WangDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Xinyu ZengDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Suyun LiDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Rui LiuDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Shuting HuangDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Yuye FuDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China.
Jie LiDepartment of Ultrasound, Qilu Hospital of Shandong University, Jinan, 250012, Shandong, China. jieli@email.sdu.edu.cn.

Funding

National Natural Science Foundation of China 82471992Taishan Scholars Program of Shandong Province tstp20230655
6 · The paper itself

Abstract

Abnormal energy metabolism patterns are common characteristics of various tumor cells, including hepatocellular carcinoma cells (HCC). HCC undergo metabolic reprogramming, upregulating the tricarboxylic acid (TCA) cycle and mitochondrial respiration to provide energy. Based on this, we constructed a novel reactive oxygen species (ROS)- and ultrasound-responsive nanodroplet (named sGTND), which were loaded with glucose-6-phosphate dehydrogenase (G6PD) siRNA and modified with glycyrrhetinic acid (GA) via GTC polymer. These sGTNDs have a particle size of approximately 300 nm, exhibit excellent biocompatibility and contrast-enhanced ultrasound imaging. By recognizing GA receptors, sGTNDs can be specifically targeted and enriched within HCC. Under the combined effect of ultrasound-targeted microbubble destruction (UTMD), sGTNDs release GA to activate the nuclear factor erythroid 2-related factor 2 (NRF2) while simultaneously releasing siRNA to inhibit G6PD. This dual action synergistically inhibits the TCA cycle, resulting in an antitumor efficacy of up to 95.1%, which is significantly higher than that observed in the control groups. Thus, the combination of sGTND and UTMD can effectively inhibit the TCA cycle through NRF2 activation and G6PD inhibition, which represents a promising therapeutic approach for HCC.

Indexed as

Carcinoma, HepatocellularCitric Acid CycleLiver NeoplasmsNanoparticlesReactive Oxygen SpeciesAnimalsCell Line, TumorGlucosephosphate DehydrogenaseGlycyrrhetinic AcidHep G2 CellsHumansMicrobubblesNF-E2-Related Factor 2RNA, Small InterferingUltrasonic WavesGlucosephosphate DehydrogenaseGlycyrrhetinic AcidNF-E2-Related Factor 2Reactive Oxygen SpeciesRNA, Small InterferingHepatocellular carcinomaNanodropletsROS-responsiveTricarboxylic acid cycleUltrasound targeted microbubble destruction

Identifiers

PMID41765880
PMCPMC13059381

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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.