Evidence map›Paper›PMID 40528526›Full record

ArticleAdvanced materials (Deerfield Beach, Fla.)2025

Artesunate Nanoplatform Targets the Serine-MAPK Axis in Cancer-Associated Fibroblasts to Reverse Photothermal Resistance in Triple-Negative Breast Cancer.

Dongdong Zheng, Jiaqi Yan, Xuejiao Liu, Zhiming Zhang, Anqi Jin, Yue Zhao, Lu Bai, Mengyao Quan, Xiuzhu Qi, Bin Fu and 10 more

Abstract read
In one paragraph

Article in Advanced materials (Deerfield Beach, Fla.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing 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

16 citing papers in PubMed.

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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

20 authors.

Dongdong ZhengDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.ORCID https://orcid.org/0000-0001-6189-9046
Jiaqi YanJoint Centre of Translational Medicine, Wenzhou Key Laboratory of Interdiscipline and Translational Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, P. R. China.
Xuejiao LiuInstitutes of Biomedical Sciences and Department of Chemistry, Fudan University, Shanghai, 200032, P. R. China.
Zhiming ZhangDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Anqi JinDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Yue ZhaoPharmaceutical Sciences Laboratory, Åbo Akademi University, Turku, FI-00520, Finland.
Lu BaiDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Mengyao QuanDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Xiuzhu QiDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Bin FuInstitutes of Biomedical Sciences and Department of Chemistry, Fudan University, Shanghai, 200032, P. R. China.
Zhigang WuDepartment of Thoracic Surgery and State Key Laboratory of Genetic Engineering, Shanghai, 200032, P. R. China.
Jin ZhouDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Han HanDepartment of Thoracic Surgery and State Key Laboratory of Genetic Engineering, Shanghai, 200032, P. R. China.
Ziqi WangDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Shiyu WangDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Chaoqiang DengDepartment of Thoracic Surgery and State Key Laboratory of Genetic Engineering, Shanghai, 200032, P. R. China.
Weijian SunJoint Centre of Translational Medicine, Wenzhou Key Laboratory of Interdiscipline and Translational Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, P. R. China.
Cai ChangDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Shichong ZhouDepartment of Ultrasound, Fudan University Shanghai Cancer Center, Shanghai, 200032, P. R. China.
Hongbo ZhangJoint Centre of Translational Medicine, Wenzhou Key Laboratory of Interdiscipline and Translational Medicine, the First Affiliated Hospital of Wenzhou Medical University, Wenzhou, 325000, P. R. China.ORCID https://orcid.org/0000-0002-1071-4416

Funding

China Postdoctoral Science Foundation 2024M760561Discipline Cluster of Oncology, Wenzhou Medical University, China z1-2023002InFLAMES Flagship 337531Joint Fund of the Zhejiang Provincial Natural Science Foundation of China BD24H180004National Natural Science Foundation of China 81830058National Natural Science Foundation of China 82071945National Natural Science Foundation of China 82311530049National Natural Science Foundation of China 82371978National Natural Science Foundation of China 82372145Research Council of FinlandResearch Project 347897Shanghai Anticancer Association EYAS PROJECT SACA-CY22C07Shanghai Committee of Science and Technology 21S31905400Solution for Health Profile 336355
6 · The paper itself

Abstract

Cancer-associated fibroblasts (CAFs) play a pivotal role in inducing photothermal therapy (PTT) resistance of triple-negative breast cancer (TNBC), but with unclear mechanism. Herein, aminoethyl anisamide-modified nano-biomimetic low-density lipoprotein (A-aLDL) is used to target deliver the PTT agent and artesunate (ARS) to both CAFs and cancer cells. Though CAFs are sensitive to PTT and notably transition to heat-resistant phenotype, the formed protective barrier is destroyed by ARS. Subsequently, the outstanding anti-tumor effects are achieved through PTT in multiple models with such kind of combination therapy. Interestingly, the mechanism is discovered that serine metabolism plays a major role in CAF resistance through spatially omics. ARS disrupts serine homeostasis, thereby attenuating the cascade activity of GTPases in MAPK pathway. Meanwhile, MAP2K7 is the most potential target for sensitizing PTT. By integrating ARS with PTT agents, the serine-MAPK axis in CAFs is successfully modulated, thereby overcoming PTT resistance in TNBC therapy.

Indexed as

Antineoplastic AgentsArtesunateCancer-Associated FibroblastsMAP Kinase Signaling SystemNanoparticlesSerineTriple Negative Breast NeoplasmsAnimalsCell Line, TumorFemaleHumansMicePhotothermal TherapyAntineoplastic AgentsArtesunateSerineartesunate nanoplatformbreast cancercancer‐associated fibroblastsphotothermal therapy

Identifiers

PMID40528526
PMCPMC12412003

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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.