Evidence map›Paper›PMID 31649305›Full record

ArticleCellular & molecular immunology2020

Macrophages reprogrammed by lung cancer microparticles promote tumor development via release of IL-1β.

Jie Chen, Weiwei Sun, Huafeng Zhang, Jingwei Ma, Pingwei Xu, Yuandong Yu, Haiqing Fang, Li Zhou, Jiadi Lv, Jing Xie and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Cellular & molecular immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 60 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Jie Chen *Department of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Weiwei Sun *Department of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Huafeng ZhangDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Jingwei MaDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Pingwei XuDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Yuandong YuDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Haiqing FangDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Li ZhouDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China.
Jiadi LvDepartment of Immunology, Institute of Basic Medical Sciences & State Key Laboratory of Medical Molecular Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 100005, Beijing, China.
Jing XieDepartment of Immunology, Institute of Basic Medical Sciences & State Key Laboratory of Medical Molecular Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 100005, Beijing, China.
Yuying LiuDepartment of Immunology, Institute of Basic Medical Sciences & State Key Laboratory of Medical Molecular Biology, Chinese Academy of Medical Sciences and Peking Union Medical College, 100005, Beijing, China.
Ke TangDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China. ketang@hust.edu.cn.
Bo HuangDepartment of Biochemistry and Molecular Biology, Tongji Medical College, Huazhong University of Science and Technology, 430030, Wuhan, China. tjhuangbo@hotmail.com.
Huazhong University of Science and Technology · CNChinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite their mutual antagonism, inflammation and immunosuppression coexist in tumor microenvironments due to tumor and immune cell interactions, but the underlying mechanism remains unclear. Previously, we showed that tumor cell-derived microparticles induce an M2 phenotype characterized by immunosuppression in tumor-infiltrating macrophages. Here, we further showed that lung cancer microparticles (L-MPs) induce macrophages to release a key proinflammatory cytokine, IL-1β, thus promoting lung cancer development. The underlying mechanism involves the activation of TLR3 and the NLRP3 inflammasome by L-MPs. More importantly, tyrosine kinase inhibitor treatment-induced L-MPs also induce human macrophages to release IL-1β, leading to a tumor-promoting effect in a humanized mouse model. These findings demonstrated that in addition to their anti-inflammatory effect, L-MPs induce a proinflammatory phenotype in tumor-infiltrating macrophages, promoting the development of inflammatory and immunosuppressive tumor microenvironments.

Indexed as

Cellular ReprogrammingAnimalsCalciumCarcinogenesisCell-Derived MicroparticlesCell Line, TumorDisease Models, AnimalFemaleHumansInterleukin-1betaLigandsLung NeoplasmsLymphocyte ActivationLysosomesMacrophagesMice, Inbred BALB CCalciumInterleukin-1betaLigandsNLR Family, Pyrin Domain-Containing 3 ProteinReactive Oxygen SpeciesRNA, UntranslatedToll-Like Receptor 3InflammasomeInterleukin-1βMacrophageTumor microparticlesTumor-repopulating cells

Identifiers

PMID31649305
PMCPMC7784894
OpenAlexW2981810532

What OpenQuestion holds

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Registered trials

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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.