Evidence map›Paper›PMID 33496784›Full record

ArticleThe Journal of experimental medicine2021

Suppression of local type I interferon by gut microbiota-derived butyrate impairs antitumor effects of ionizing radiation.

Kaiting Yang, Yuzhu Hou, Yuan Zhang, Hua Liang, Anukriti Sharma, Wenxin Zheng, Liangliang Wang, Rolando Torres, Ken Tatebe, Steven J Chmura and 4 more

Erratum issuedOpen access · bronzeAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 82 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
82citing papers in PubMed, 1 pooled it
6.1field-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

82 citing papers in PubMed, 1 synthesis or guideline pooled it, 113 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 3 institutions in 1 country.

Kaiting YangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Yuzhu HouDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Yuan ZhangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Hua LiangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Anukriti SharmaDepartment of Pediatrics, University of California, San Diego, La Jolla, CA.
Wenxin ZhengDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Liangliang WangDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Rolando TorresDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Ken TatebeDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Steven J ChmuraDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Sean P PitrodaDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
Jack A GilbertDepartment of Pediatrics, University of California, San Diego, La Jolla, CA.
Yang-Xin FuDepartment of Pathology, University of Texas Southwestern Medical Center, Dallas, TX.
Ralph R WeichselbaumDepartment of Radiation and Cellular Oncology, University of Chicago, Chicago, IL.
University of Chicago · USScripps Institution of Oceanography · USThe University of Texas Southwestern Medical Center · US

Funding

Microbiota and the anti-tumor action of anti-CD47 immunomodulation.R21CA231273 · NCI · UNIVERSITY OF CHICAGO · PI WEICHSELBAUM, RALPH R · 2019 to 2020
$388k
(PQ10) Understanding How Commensal Microbiota Affect the Anti-tumor Action of RadiotherapyR21CA227528 · NCI · UNIVERSITY OF CHICAGO · PI WEICHSELBAUM, RALPH R · 2018 to 2019
$381k
NCI NIH HHS R21 CA227528NCI NIH HHS R21 CA231273
6 · The paper itself

Abstract

The antitumor effects of ionizing radiation (IR) are mediated in part through activation of innate and adaptive immunity. Here we report that gut microbiota influences tumor control following IR. Vancomycin decreased the abundance of butyrate-producing gut bacteria and enhanced antitumor responses to IR. Oral administration of Lachnospiraceae, a family of vancomycin-sensitive bacteria, was associated with increased systemic and intratumoral butyric acid levels and impaired the efficacy of IR in germ-free (GF) mice. Local butyrate inhibited STING-activated type I IFN expression in dendritic cells (DCs) through blockade of TBK1 and IRF3 phosphorylation, which abrogated IR-induced tumor-specific cytotoxic T cell immune responses without directly protecting tumor cells from radiation. Our findings demonstrate that the selective targeting of butyrate-producing microbiota may provide a novel therapeutic option to enhance tumor radiation sensitivity.

Indexed as

Gastrointestinal MicrobiomeRadiation, IonizingAdaptive ImmunityAdministration, OralAnimalsAntineoplastic AgentsBacteriaButyratesGastrointestinal TractImmunity, InnateInterferon Type IMiceMice, Inbred C57BLMyeloid CellsT-LymphocytesVancomycinAntineoplastic AgentsButyratesInterferon Type IVancomycin

Identifiers

PMID33496784
PMCPMC7844434
OpenAlexW3123341271

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.