Evidence map›Paper›PMID 38380506›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2024

A Multifunctional Bimetallic Nanoplatform for Synergic Local Hyperthermia and Chemotherapy Targeting HER2-Positive Breast Cancer.

Li Zhao, Fei Chang, Yao Tong, Jiawei Yin, Jiawen Xu, Hui Li, Lutao Du, Yanyan Jiang

Open access · goldAbstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
6.2field-weighted citation impact, top 3% of its field
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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 citations in OpenAlex.

  1. Pooled it
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  5. Review
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  12. In Situ Construction of Hollow Coral-Like Porous S-Doped g-CAdvanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
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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

8 authors at 4 institutions in 1 country.

Li ZhaoLiquid-Solid Structural Evolution & Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Fei ChangThe Second Hospital of Shandong University, Jinan, Shandong, 250033, China.
Yao TongThe Second Hospital of Shandong University, Jinan, Shandong, 250033, China.
Jiawei YinThe Second Hospital of Shandong University, Jinan, Shandong, 250033, China.
Jiawen XuDepartment of Pathology, Shandong Provincial Hospital affiliated to Shandong First Medical University, Jinan, Shandong, 250021, China.
Hui LiLiquid-Solid Structural Evolution & Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.
Lutao DuDepartment of Clinical Laboratory, Qilu Hospital of Shandong University, Jinan, Shandong, 250012, China.
Yanyan JiangLiquid-Solid Structural Evolution & Processing of Materials (Ministry of Education), School of Materials Science and Engineering, Shandong University, Jinan, Shandong, 250061, China.ORCID 0000-0002-7866-4689
Second Hospital of Shandong University · CNShandong University · CNShandong Provincial Hospital · CNShanghai Clinical Research Center · CN

Funding

Beijing Xisike Clinical Oncology Research Foundation Y-HR-2019-0212Jinan Science and Technology Bureau 2020GXRC019Ministry of Industry and Information Technology of the People's Republic of China 2020-370104-34-03-043952-01-11National Natural Science Foundation of China 52101287Taishan Scholar Foundation of Shandong Province
6 · The paper itself

Abstract

Anti-HER2 (human epidermal growth factor receptor 2) therapies significantly increase the overall survival of patients with HER2-positive breast cancer. Unfortunately, a large fraction of patients may develop primary or acquired resistance. Further, a multidrug combination used to prevent this in the clinic places a significant burden on patients. To address this issue, this work develops a nanotherapeutic platform that incorporates bimetallic gold-silver hollow nanoshells (AuAg HNSs) with exceptional near-infrared (NIR) absorption capability, the small-molecule tyrosine kinase inhibitor pyrotinib (PYR), and Herceptin (HCT). This platform realizes targeted delivery of multiple therapeutic effects, including chemo-and photothermal activities, oxidative stress, and immune response. In vitro assays reveal that the HCT-modified nanoparticles exhibit specific recognition ability and effective internalization by cells. The released PYR inhibit cell proliferation by downregulating HER2 and its associated pathways. NIR laser application induces a photothermal effect and tumor cell apoptosis, whereas an intracellular reactive oxygen species burst amplifies oxidative stress and triggers cancer cell ferroptosis. Importantly, this multimodal therapy also promotes the upregulation of genes related to TNF and NF-κB signaling pathways, enhancing immune activation and immunogenic cell death. In vivo studies confirm a significant reduction in tumor volume after treatment, substantiating the potential effectiveness of these nanocarriers.

Indexed as

Breast NeoplasmsErb-b2 Receptor Tyrosine KinasesGoldHyperthermia, InducedAnimalsAntineoplastic AgentsCell Line, TumorCell ProliferationCombined Modality TherapyDisease Models, AnimalFemaleHumansMetal NanoparticlesMiceSilverTrastuzumabAntineoplastic AgentsERBB2 protein, humanErb-b2 Receptor Tyrosine KinasesGoldSilverTrastuzumabbimetallic AuAg HNSschemo‐phototherapyHER2‐positive breast cancernanotherapeutic platformpyrotinib

Identifiers

PMID38380506
PMCPMC11040336
OpenAlexW4392018082

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.