Evidence map›Paper›PMID 42053823›Full record

ArticleMikrochimica acta2026

Multifunctional double hairpin DNA polydopamine nano-system for "switch-on" detection and intervention of high-grade dysplastic nodules.

Jie Zhou, Junfen Feng, Xiaomeng Dong, Tong Zhang, Yuxin Wei, Yanzi Wang, Chenyu Shi

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Article in Mikrochimica acta, 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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5 · Who and what money

Authors and funding

7 authors.

Jie ZhouSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China. jie_0822@163.com.
Junfen FengSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Xiaomeng DongSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Tong ZhangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Yuxin WeiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Yanzi WangSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.
Chenyu ShiSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou, 450001, China.

Funding

Key Scientific Research Project Plan of Colleges and Universities in Henan Province 26A350012National Natural Science Foundation of China U1904135
6 · The paper itself

Abstract

The 5-year survival rate of early-stage hepatocellular carcinoma (HCC) patients remains only 60%, largely due to the inability to achieve ultra-early detection and safe, minimally invasive intervention of its premalignant precursor-high-grade dysplastic nodules (HGDN). Current clinical practice faces an unresolved dilemma: conventional imaging has limited sensitivity for HGDN, no standardized minimally invasive intervention exists, and no integrated platform enables synchronous detection, boundary localization and on-demand intervention, despite HGDN 80.8% 5-year HCC progression rate. To address these core challenges, we developed a multifunctional dual-hairpin DNA polydopamine nano-system (H/R@PDA-GC) targeting miRNA-224, a biomarker consistently upregulated during HGDN malignant transformation.This system enables specific detection of miRNA-224 with an ultra-low limit of detection (LOD) of 0.068 pM. Clinically, there is a 3-5-year natural history window from HGDN formation to clinically diagnosable early HCC; thus, this system provides a potential technical tool for the ultra-early warning of HCC at the precancerous stage. It simultaneously activates near-infrared fluorescence for targeted imaging of HGDN to precisely delineate lesion boundaries, and leverages its efficient photothermal conversion capability to achieve effective ablation of HGDN in validated murine models. Both cellular and animal studies confirmed its good in vitro and short-term in vivo biocompatibility, significant anti-inflammatory and antioxidant effects, and therapeutic efficacy, addressing the dual clinical needs of ultra-early detection and safe intervention of premalignant lesions. Consequently, H/R@PDA-GC provides an integrated theranostic strategy, which has potential clinical value for reducing the risk of HCC progression, and lays a foundation for ultra-early intervention of HCC precancerous lesions.Clinical trial number. Not applicable.

Indexed as

Carcinoma, HepatocellularDNAIndolesLiver NeoplasmsNanoparticlesPolymersAnimalsHumansLimit of DetectionMiceMicroRNAsDNAIndolesMicroRNAspolydopaminePolymersHGDNIntervention of premalignant lesionsmiRNA-224PDA

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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.