Evidence map›Paper›PMID 39799561›Full record

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

Controlled Inflammation Drives Neutrophil-Mediated Precision Drug Delivery in Heterogeneous Tumors.

Yunfei Guo, Yiming Li, Jianmin Li, Haoran Cai, Kangkang Liu, Dengyi Duan, Wenyi Zhang, Gang Han, Yang Zhao

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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
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

9 authors.

Yunfei GuoDepartment of Radiology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Yiming LiDepartment of Radiology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Jianmin LiTianjin Institute of Urology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Haoran CaiDepartment of Radiology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Kangkang LiuTianjin Institute of Urology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Dengyi DuanDepartment of Radiology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Wenyi ZhangDepartment of Radiology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.
Gang HanBiochemistry and Molecular Biotechnology, University of Massachusetts Chan Medical School, Worcester, MA, 01605, USA.ORCID https://orcid.org/0000-0002-2300-5862
Yang ZhaoDepartment of Radiology, The Second Hospital of Tianjin Medical University, Tianjin, 300211, P. R. China.

Funding

National Natural Science Foundation of China 81872106National Natural Science Foundation of China 82272804National Natural Science Foundation of China 91959114Natural Science Foundation of Tianjin 22JCQNJC01700Research Innovation Project of Tianjin Municipal Education Commission 2020YJSB161Scientific and Technological Research Program of Tianjin Health Commission TJWJ2022XK015Scientific and Technological Research Program of Tianjin Municipal Education Commission 2019ZD025Tianjin Key Medical Discipline (Specialty) Construction Project TJYXZDXK-070CTianjin Science Fund for Distinguished Young Scholars 20JCJQJC00270
6 · The paper itself

Abstract

Tumor heterogeneity remains a formidable obstacle in targeted cancer therapy, often leading to suboptimal treatment outcomes. This study presents an innovative approach that harnesses controlled inflammation to guide neutrophil-mediated drug delivery, effectively overcoming the limitations imposed by tumor heterogeneity. By inducing localized inflammation within tumors using lipopolysaccharide, it significantly amplify the recruitment of drug-laden neutrophils to tumor sites, irrespective of specific tumor markers. This strategy not only enhances targeted drug delivery but also triggers the release of neutrophil extracellular traps, further potentiating the anti-tumor effect. Crucially, this study demonstrates that potential systemic inflammatory responses can be effectively mitigated through neutrophil transfusion, ensuring the safety and clinical viability of this approach. In a murine breast cancer model, the method significantly impedes tumor growth compared to conventional treatments. This work offers a versatile strategy for precise drug delivery across diverse tumor types. The findings pave the way for more effective and broadly applicable cancer treatments, potentially addressing the long-standing challenge of tumor heterogeneity.

Indexed as

Antineoplastic AgentsBreast NeoplasmsDrug Delivery SystemsInflammationNeutrophilsAnimalsCell Line, TumorDisease Models, AnimalExtracellular TrapsFemaleHumansMiceAntineoplastic AgentsinflammationnanomedicineNeutrophiltumor targeted therapy

Identifiers

PMID39799561
PMCPMC11923894

What Socratic 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 Socratic graph.