Evidence map›Paper›PMID 39421752›Full record

ReviewFrontiers in immunology2024

Clinical applications of STING agonists in cancer immunotherapy: current progress and future prospects.

Bin Wang, Wanpeng Yu, Hongfei Jiang, Xiangwei Meng, Dongmei Tang, Dan Liu

Abstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 86 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
86citing papers in PubMed, 2 pooled it
–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

86 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Review
  6. Article
  7. Innate immunity: current understandings and future perspectives.Signal transduction and targeted therapy · 2026
    Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Discovery of MK-2118, a Small-Molecule Agonist of STING.ACS medicinal chemistry letters · 2026
    Article
  15. Article
  16. Article
  17. Article
  18. A PI(3,5)PNature communications · 2026
    Article
  19. Albumin-Bound STING Agonist Reprograms HSPCs to Antitumor Neutrophils Enhancing CD8Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  20. Review

26 more citing papers are in PubMed but not listed here.

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

6 authors.

Bin Wang *The Afffliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Wanpeng Yu *The Afffliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Hongfei JiangThe Afffliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Xiangwei MengDepartment of Drug Clinical Trials, Zibo Central Hospital, Zibo, China.
Dongmei TangThe Afffliated Hospital of Qingdao University, Qingdao University, Qingdao, China.
Dan LiuMedical Education Department, Guangdong Provincial People's Hospital, Zhuhai Hospital (Jinwan Central Hospital of Zhuhai), Zhuhai, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The STING (Stimulator of Interferon Genes) pathway is pivotal in activating innate immunity, making it a promising target for cancer immunotherapy. STING agonists have shown potential in enhancing immune responses, particularly in tumors resistant to traditional therapies. This scholarly review examines the diverse categories of STING agonists, encompassing CDN analogues, non-CDN chemotypes, CDN-infused exosomes, engineered bacterial vectors, and hybrid structures of small molecules-nucleic acids. We highlight their mechanisms, clinical trial progress, and therapeutic outcomes. While these agents offer significant promise, challenges such as toxicity, tumor heterogeneity, and delivery methods remain obstacles to their broader clinical use. Ongoing research and innovation are essential to overcoming these hurdles. STING agonists could play a transformative role in cancer treatment, particularly for patients with hard-to-treat malignancies, by harnessing the body's immune system to target and eliminate cancer cells.

Indexed as

ImmunotherapyMembrane ProteinsNeoplasmsAnimalsHumansImmunity, InnateSignal TransductionSTING ProteinMembrane ProteinsSTING1 protein, humanSTING Proteincancer immunotherapycGAS-STING pathwayinnate immunitySTING agoniststumor microenvironment

Identifiers

PMID39421752
PMCPMC11483357

What OpenQuestion holds

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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.