Evidence map›Paper›PMID 29358709›Full record

ArticleNature immunology2018

Tumor-derived exosomes antagonize innate antiviral immunity.

Liang Gao, Lin Wang, Tong Dai, Ke Jin, Zhengkui Zhang, Shuai Wang, Feng Xie, Pengfei Fang, Bing Yang, Huizhe Huang and 3 more

Abstract read
PubMed Publisher
In one paragraph

Article in Nature immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 110 papers.

0numbers the graph read from it
0cells of the map it votes in
110citing papers in PubMed
10.2field-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.

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

110 citing papers in PubMed, 195 citations in OpenAlex.

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 5 institutions in 3 countries.

Liang GaoLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China.
Lin WangInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Tong DaiLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China.
Ke JinLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China.
Zhengkui ZhangLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China.
Shuai WangInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China.
Feng XieLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China.
Pengfei FangLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China.
Bing YangDepartment of Pharmaceutical Chemistry and the Cardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.
Huizhe HuangFaculty of Basic Medical Sciences, Chonqing Medical University, Chongqing, China.
Hans van DamDepartment of Molecular Cell Biology, Cancer Genomics Centre Netherlands, Leiden University Medical Center, Leiden, The Netherlands.
Fangfang ZhouInstitutes of Biology and Medical Sciences, Soochow University, Suzhou, China. zhoufangfang@suda.edu.cn.ORCID 0000-0003-1870-7584
Long ZhangLife Sciences Institute and Innovation Center for Cell Signaling Network, Hangzhou, Zhejiang, China. l_zhang@zju.edu.cn.ORCID 0000-0001-8139-0474
Soochow University · CNChongqing Medical University · CNLeiden University Medical Center · NLUniversity of California, San Francisco · USZhejiang Lab · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Malignancies can compromise innate immunity, but the mechanisms of this are largely unknown. Here we found that, via tumor-derived exosomes (TEXs), cancers were able to transfer activated epidermal growth factor receptor (EGFR) to host macrophages and thereby suppress innate antiviral immunity. Screening of the human kinome identified the kinase MEKK2 in macrophages as an effector of TEX-delivered EGFR that negatively regulated the antiviral immune response. In the context of experimental tumor implantation, MEKK2-deficient mice were more resistant to viral infection than were wild-type mice. Injection of TEXs into mice reduced innate immunity, increased viral load and increased morbidity in an EGFR- and MEKK2-dependent manner. MEKK2 phosphorylated IRF3, a transcription factor crucial for the production of type I interferons; this triggered poly-ubiquitination of IRF3 and blocked its dimerization, translocation to the nucleus and transcriptional activity after viral infection. These findings identify a mechanism by which cancer cells can dampen host innate immunity and potentially cause patients with cancer to become immunocompromised.

Indexed as

AdultAnimalsErbB ReceptorsExosomesFemaleHumansImmunity, InnateImmunocompromised HostMacrophagesMaleMAP Kinase Kinase Kinase 2MiceMice, Inbred C57BLMice, KnockoutMiddle AgedNeoplasmsErbB ReceptorsMAP Kinase Kinase Kinase 2

Identifiers

PMID29358709
OpenAlexW2791742323

What OpenQuestion holds

Textmetadata
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.