Evidence map›Paper›PMID 42211359›Full record

ArticleRSC advances2026

A Natural product-based composite nanozyme synergistically induces ferroptosis for lung cancer therapy.

Yishun Jin, Chen Huang, Zhenbo Geng, Huang Li, Huiqing Ge, Pengfei Wang, Chaojun Dai, Jun Li, Xiaohua Yan, Chen Li and 1 more

Abstract read
In one paragraph

Article in RSC advances, 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.

Yishun JinDepartment of Traditional Chinese Medicine, Fuzhou University Affiliated Provincial Hospital Fuzhou 350001 China yanxiaohua@fjsl.com.cn.
Chen HuangDepartment of Thoracic Surgery, Fuzhou University Affiliated Provincial Hospital Fuzhou China.
Zhenbo GengDepartment of Traditional Chinese Medicine, Fuzhou University Affiliated Provincial Hospital Fuzhou 350001 China yanxiaohua@fjsl.com.cn.
Huang LiSchool of Pharmacy, Fujian University of Traditional Chinese Medicine Fuzhou 350122 China.
Huiqing GeDepartment of Thoracic Surgery, Fuzhou University Affiliated Provincial Hospital Fuzhou China.
Pengfei WangDepartment of Traditional Chinese Medicine, Fuzhou University Affiliated Provincial Hospital Fuzhou 350001 China yanxiaohua@fjsl.com.cn.ORCID https://orcid.org/0000-0002-4084-2267
Chaojun DaiDepartment of Traditional Chinese Medicine, Fuzhou University Affiliated Provincial Hospital Fuzhou 350001 China yanxiaohua@fjsl.com.cn.
Jun LiDepartment of Critical Care Medicine, Fuzhou University Affiliated Provincial Hospital, Fujian Provincial Hospital Fuzhou 350001 China.
Xiaohua YanDepartment of Traditional Chinese Medicine, Fuzhou University Affiliated Provincial Hospital Fuzhou 350001 China yanxiaohua@fjsl.com.cn.
Chen LiCollege of Pharmacy, Hainan Academy of Medical Sciences, Hainan Medical University Haikou Hainan 571199 China hy0211100@muhn.edu.cn.ORCID https://orcid.org/0009-0002-4769-7581
Yan ZhengDepartment of Oncology, Fuzhou University Affiliated Provincial Hospital China zhengyan0996@fzu.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The treatment of lung cancer remains a significant clinical challenge. Inducing ferroptosis is a promising therapeutic strategy to overcome treatment resistance in lung cancer. Herein, we report a composite nanozyme, Fe@Arc, engineered by coordinating arctigenin with iron ions followed by a high-temperature carbonization. This fabrication method yielded a nanozyme with a high drug-loading capacity and controlled release kinetics. Following intravenous administration, Fe@Arc efficiently accumulated at the tumor site owing to its enhanced permeability and retention effect. In the tumor site, it exerted a potent anti-tumor effect by catalyzing the Fenton reaction and releasing arctigenin, which synergistically triggered ferroptosis in cancer cells. This work presents a multifaceted platform that not only overcomes the pharmacological limitations of herbal extracts but also establishes a robust framework for developing novel ferroptosis inducers, demonstrating significant potential for clinical translation.

Identifiers

PMID42211359
PMCPMC13213561

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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.