Evidence map›Paper›PMID 31704921›Full record

ArticleNature communications2019

An inhalable nanoparticulate STING agonist synergizes with radiotherapy to confer long-term control of lung metastases.

Yang Liu, William N Crowe, Lulu Wang, Yong Lu, W Jeffrey Petty, Amyn A Habib, Dawen Zhao

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 129 papers.

0numbers the graph read from it
0cells of the map it votes in
129citing papers in PubMed
8.4field-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

129 citing papers in PubMed, 236 citations in OpenAlex.

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  19. CD169Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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69 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

7 authors at 2 institutions in 1 country.

Yang LiuDepartment of Biomedical Engineering, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
William N CroweDepartment of Biomedical Engineering, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Lulu WangDepartment of Biomedical Engineering, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Yong LuDepartment of Microbiology and Immunology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
W Jeffrey PettyDepartment of Medicine, Section on Hematology and Oncology, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA.
Amyn A HabibDepartment of Neurology and Neurotherapeutics, University of Texas Southwestern Medical Center and VA North Texas Medical Center, Dallas, TX, 75390, USA.ORCID http://orcid.org/0000-0003-4164-9028
Dawen ZhaoDepartment of Biomedical Engineering, Wake Forest School of Medicine, Winston-Salem, NC, 27157, USA. dawzhao@wakehealth.edu.
Wake Forest University · USTexas Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mounting evidence suggests that the tumor microenvironment is profoundly immunosuppressive. Thus, mitigating tumor immunosuppression is crucial for inducing sustained antitumor immunity. Whereas previous studies involved intratumoral injection, we report here an inhalable nanoparticle-immunotherapy system targeting pulmonary antigen presenting cells (APCs) to enhance anticancer immunity against lung metastases. Inhalation of phosphatidylserine coated liposome loaded with STING agonist cyclic guanosine monophosphate-adenosine monophosphate (NP-cGAMP) in mouse models of lung metastases enables rapid distribution of NP-cGAMP to both lungs and subsequent uptake by APCs without causing immunopathology. NP-cGAMP designed for enhanced cytosolic release of cGAMP stimulates STING signaling and type I interferons production in APCs, resulting in the pro-inflammatory tumor microenvironment in multifocal lung metastases. Furthermore, fractionated radiation delivered to one tumor-bearing lung synergizes with inhaled NP-cGAMP, eliciting systemic anticancer immunity, controlling metastases in both lungs, and conferring long-term survival in mice with lung metastases and with repeated tumor challenge.

Indexed as

ImmunotherapyNanoparticlesRadiotherapyAdministration, InhalationAnimalsAntigen-Presenting CellsDendritic CellsInterferon Type ILiposomesLungLung NeoplasmsMacrophagesMelanoma, ExperimentalMembrane ProteinsMiceNucleotides, Cycliccyclic guanosine monophosphate-adenosine monophosphateInterferon Type ILiposomesMembrane ProteinsNucleotides, CyclicPhosphatidylserinesSting1 protein, mouseSTING Protein

Identifiers

PMID31704921
PMCPMC6841721
OpenAlexW2985862606

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.