Evidence map›Paper›PMID 31679519›Full record

ReviewMolecular cancer2019

STING: a master regulator in the cancer-immunity cycle.

Yuanyuan Zhu, Xiang An, Xiao Zhang, Yu Qiao, Tongsen Zheng, Xiaobo Li

Registry-linked trialOpen access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04998422 (Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of HG381 as Monotherapy in Patients With Advanced Solid Tumors), which is not on this map. Cited by 252 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
252citing papers in PubMed, 3 pooled it
14.6field-weighted citation impact, top 1% 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.

NCT04998422 phase1recruitingnot on this mapstarted 2021, after this paper: background citation

Phase 1 Study Evaluating the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of HG381 as Monotherapy in Patients With Advanced Solid Tumors

TypeinterventionalSponsorHitGen Inc.Ran2021 to 2025Enrolled57ConditionsAdvanced Solid TumorArmsHG381
3 · Its place in the literature

Who cites it

252 citing papers in PubMed, 3 syntheses or guidelines pooled it, 423 citations in OpenAlex.

  1. Pooled it
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  7. Mitochondrial dynamics and T cells immunity in cancer.Biochemistry and biophysics reports · 2026
    Review
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  19. ROS-Responsive MnOJournal of nanobiotechnology · 2026
    Article
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192 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 at 2 institutions in 1 country.

Yuanyuan ZhuDepartment of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081, China.
Xiang AnDepartment of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081, China.
Xiao ZhangDepartment of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081, China.
Yu QiaoDepartment of Histology and Embryology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081, China.
Tongsen ZhengDepartment of Gastrointestinal Medical Oncology, Harbin Medical University Cancer Hospital, No.150 Haping Road, Nangang District, Harbin, 150081, China. zhengtongsen@126.com.
Xiaobo LiDepartment of Pathology, Harbin Medical University, No. 157 Baojian Road, Nangang District, Harbin, 150081, China. lixiaobo@ems.hrbmu.edu.cn.
Harbin Medical University · CNThird Affiliated Hospital of Harbin Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The aberrant appearance of DNA in the cytoplasm triggers the activation of cGAS-cGAMP-STING signaling and induces the production of type I interferons, which play critical roles in activating both innate and adaptive immune responses. Recently, numerous studies have shown that the activation of STING and the stimulation of type I IFN production are critical for the anticancer immune response. However, emerging evidence suggests that STING also regulates anticancer immunity in a type I IFN-independent manner. For instance, STING has been shown to induce cell death and facilitate the release of cancer cell antigens. Moreover, STING activation has been demonstrated to enhance cancer antigen presentation, contribute to the priming and activation of T cells, facilitate the trafficking and infiltration of T cells into tumors and promote the recognition and killing of cancer cells by T cells. In this review, we focus on STING and the cancer immune response, with particular attention to the roles of STING activation in the cancer-immunity cycle. Additionally, the negative effects of STING activation on the cancer immune response and non-immune roles of STING in cancer have also been discussed.

Indexed as

Disease SusceptibilityImmunomodulationAnimalsAntigens, NeoplasmGene Expression Regulation, NeoplasticHumansImmunity, InnateImmunotherapyInterferon Type IMembrane ProteinsNeoplasmsSignal TransductionSTING ProteinAntigens, NeoplasmInterferon Type IMembrane ProteinsSTING1 protein, humanSTING Protein

Identifiers

PMID31679519
PMCPMC6827255
OpenAlexW2988506530

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.