Evidence map›Paper›PMID 34315904›Full record

ArticleNature communications2021

STING suppresses bone cancer pain via immune and neuronal modulation.

Kaiyuan Wang, Christopher R Donnelly, Changyu Jiang, Yihan Liao, Xin Luo, Xueshu Tao, Sangsu Bang, Aidan McGinnis, Michael Lee, Matthew J Hilton and 1 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 91 papers.

0numbers the graph read from it
0cells of the map it votes in
91citing papers in PubMed
7.1field-weighted citation impact, top 2% 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.

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

91 citing papers in PubMed, 133 citations in OpenAlex.

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31 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

11 authors at 2 institutions in 1 country.

Kaiyuan Wang *Center for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA. kywang@tmu.edu.cn.
Christopher R Donnelly *Center for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA. christopher.donnelly@duke.edu.ORCID 0000-0003-2487-8881
Changyu JiangCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Yihan LiaoDepartment of Pharmacology and Cancer Biology, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0002-2622-9036
Xin LuoCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Xueshu TaoCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Sangsu BangCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0002-9092-0075
Aidan McGinnisCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0002-9146-2205
Michael LeeCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA.
Matthew J HiltonDepartment of Orthopedic Surgery, Duke University Medical Center, Durham, NC, USA.ORCID 0000-0003-3165-267X
Ru-Rong JiCenter for Translational Pain Medicine, Department of Anesthesiology, Duke University Medical Center, Durham, NC, USA. ru-rong.ji@duke.edu.ORCID 0000-0002-9355-3688
Duke Medical Center · USDuke University · US

Funding

INTEGRATED TRAINING IN ANESTHESIOLOGY RESEARCHT32GM008600 · NIGMS · DUKE UNIVERSITY · PI Miriam Treggiari · 1996 to 2026
$6.6M
Notch Signaling in Joint Cartilage Maintenance and ArthritisR01AR063071 · NIAMS · UNIVERSITY OF ROCHESTER · PI HILTON, MATTHEW J. · 2012 to 2021
$3.9M
Notch Signaling in Endochondral Bone DevelopmentR01AR071722 · NIAMS · DUKE UNIVERSITY · PI HILTON, MATTHEW J. · 2018 to 2022
$1.8M
NIAMS NIH HHS R01 AR063071NIAMS NIH HHS R01 AR071722NIGMS NIH HHS T32 GM008600
6 · The paper itself

Abstract

Patients with advanced stage cancers frequently suffer from severe pain as a result of bone metastasis and bone destruction, for which there is no efficacious treatment. Here, using multiple mouse models of bone cancer, we report that agonists of the immune regulator STING (stimulator of interferon genes) confer remarkable protection against cancer pain, bone destruction, and local tumor burden. Repeated systemic administration of STING agonists robustly attenuates bone cancer-induced pain and improves locomotor function. Interestingly, STING agonists produce acute pain relief through direct neuronal modulation. Additionally, STING agonists protect against local bone destruction and reduce local tumor burden through modulation of osteoclast and immune cell function in the tumor microenvironment, providing long-term cancer pain relief. Finally, these in vivo effects are dependent on host-intrinsic STING and IFN-I signaling. Overall, STING activation provides unique advantages in controlling bone cancer pain through distinct and synergistic actions on nociceptors, immune cells, and osteoclasts.

Indexed as

AnalgesicsAnimalsBone NeoplasmsCancer PainCell Line, TumorDisease Models, AnimalFemaleFemurGanglia, SpinalHomeodomain ProteinsHyperalgesiaInterferonsMaleMammary Neoplasms, AnimalMembrane ProteinsMiceAnalgesicsHomeodomain ProteinsIfnar1 protein, mouseInterferonsMembrane ProteinsRAG-1 proteinReceptor, Interferon alpha-betaSting1 protein, mouseSTING ProteinvadimezanXanthones

Identifiers

PMID34315904
PMCPMC8316360
OpenAlexW3183406047

What OpenQuestion 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 OpenQuestion graph.