Evidence map›Paper›PMID 41146651›Full record

ReviewInternational journal of nanomedicine2025

Nanodelivery Strategies for STING Agonists: Toward Efficient Cancer Immunotherapy.

Meng Zhang, Yating Ji, Mingxia Liu, Yang Liu, Shiyu Tong, Yuqing Cai, Mengjiao Liu, Na Qu

Abstract readReview
In one paragraph

Review in International journal of nanomedicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Review
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.

Meng ZhangSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.
Yating JiSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.ORCID 0009-0005-6942-7867
Mingxia LiuSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.
Yang LiuSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.
Shiyu TongSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.
Yuqing CaiSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.
Mengjiao LiuInstitute for Experimental Molecular Imaging, RWTH Aachen University Clinic, Aachen, North Rhine-Westphalia, 52074, Germany.
Na QuSchool of Pharmaceutical Science, Liaoning University, Shenyang, 110036, People's Republic of China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

cGAS-STING (cyclic GMP-AMP synthetase-interferon gene stimulator) signaling pathway has great potential in tumor treatment, and its superior performance in tumor treatment makes it a new method for tumor treatment. However, the delivery of STING agonists alone has some limitations, such as easy degradation and low bioavailability. Moreover, STING agonists are usually injected intratumorally to avoid systemic side effects caused by strong immune responses, which is not suitable for metastatic lesions. Using nanocarriers to deliver STING agonists can overcome these limitations to some extent. This review explores the collaborative foundation between nanodelivery systems and the STING signaling pathway. It systematically summarizes the existing types of STING agonists and the types of nanoscale delivery systems and analyzes the delivery strategies of STING agonist delivery systems from multiple aspects, including the tumor microenvironment (TME), tumor cell targeting, multifunctional integrated drug delivery systems, and novel biomaterial. The review elaborates on the practical applications of these strategies as well as the challenges and problems they face. Finally, it analyzes and discusses the potential future directions of STING nanodelivery systems, aiming to provide references for research in related fields and to promote the efficient application of STING agonists in cancer therapy.

Indexed as

ImmunotherapyMembrane ProteinsNanoparticle Drug Delivery SystemNeoplasmsAnimalsDrug Delivery SystemsHumansNanomedicineNanoparticlesSignal TransductionSTING ProteinTumor MicroenvironmentMembrane ProteinsNanoparticle Drug Delivery SystemSTING1 protein, humanSTING ProteinAnti-tumor therapycGAS-STINGDelivery strategyDrug delivery systemSynergistic basis

Identifiers

PMID41146651
PMCPMC12554319

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.