Evidence map›Paper›PMID 40019387›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

A CLDN18.2-Targeted Nanoplatform Manipulates Magnetic Hyperthermia Spatiotemporally for Synergistic Immunotherapy in Gastric Cancer.

Xueying Wang, Hui Hui, Jing Han, Ting Guo, Yiding Wang, Lin Meng, Cong Chen, Jie He, Xiaoyong Guo, Fuyu Zhong and 5 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
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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

15 authors.

Xueying WangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Hui HuiCAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Jing HanKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Ting GuoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Yiding WangKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Lin MengKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Biochemistry and Molecular Biology, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Cong ChenKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Jie HeKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Xiaoyong GuoKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Fuyu ZhongKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Hong DuKey Laboratory of Carcinogenesis and Translational Research (Ministry of Education), Gastrointestinal Cancer Translational Research, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Jie TianSchool of Engineering Medicine & School of Biological Science and Medical Engineering, Beihang University, Beijing, 100191, China.
Xiaofang XingState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Carcinogenesis and Translational Research, Gastrointestinal Cancer Centre, Peking University Cancer Hospital & Institute, Beijing, 100142, China.
Yang DuCAS Key Laboratory of Molecular Imaging, Institute of Automation, Chinese Academy of Sciences, Beijing, 100190, China.
Jiafu JiState Key Laboratory of Holistic Integrative Management of Gastrointestinal Cancers, Beijing Key Laboratory of Carcinogenesis and Translational Research, Gastrointestinal Cancer Centre, Peking University Cancer Hospital & Institute, Beijing, 100142, China.ORCID https://orcid.org/0000-0001-6878-5543

Funding

Joint Fund for Key Projects of National Natural Science Foundation of China U20A20371Joint Fund for Key Projects of National Natural Science Foundation of China U23A20463Joint Fund for Key Projects of National Natural Science Foundation of China U24A20731National Natural Science Foundation of China 62027901National Natural Science Foundation of China 82272111National Natural Science Foundation of China 82272889National Natural Science Foundation of China 82473157National Natural Science Foundation of China 92159303National Natural Science Foundation of China 92359304Natural Science Foundation of Beijing 7222023Natural Science Foundation of Beijing 7252292Natural Science Foundation of Beijing JQ22023Natural Science Foundation of Beijing L248059Science Foundation of Peking University Cancer Hospital KC2403Science Foundation of Peking University Cancer Hospital XKFZ2401
6 · The paper itself

Abstract

Precision treatment of gastric cancer requires specific biomarkers, and CLDN18.2 emerges as a promising target for patients' stratification and therapeutic guidance. In 563 cases, 54.4% of patients are identified as CLDN18.2-positive, with CLDN18.2 expression negatively correlated with immune-related factors like PD-L1, indicating a "cold" tumor microenvironment. Here, a novel CLDN18.2 monoclonal antibody 1D5 is created with superior high specificity and affinity, and the antibody-dependent fluorescence-magnetic nanoparticle is developed for specific detection and magnetic hyperthermia (MHT). Under the assistance of sensitive fluorescence and deep-penetrating magnetic particle imaging for tracing and timing the optimal nanoparticle dosage, MHT induces robust immunogenic response via DNA mismatch repair and tumor-associated antigen release. It recruits CD11c

Indexed as

ClaudinsHyperthermia, InducedImmunotherapyStomach NeoplasmsAnimalsCell Line, TumorFemaleHumansMiceTumor MicroenvironmentClaudinsCLDN18 protein, humanCLDN18.2gastric cancerimmunotherapymagnetic hyperthermiamolecular imagingnanoparticle

Identifiers

PMID40019387
PMCPMC12021038

What OpenQuestion holds

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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.