Evidence map›Paper›PMID 31318609›Full record

ArticleFASEB journal : official publication of the Federation of American Societies for Experimental Biology2019

AhR-ROR-γt complex is a therapeutic target for MAP4K3/GLK

Huai-Chia Chuang, Yi-Ming Chen, Ming-Han Chen, Wei-Ting Hung, Huang-Yu Yang, Yang-Hao Tseng, Tse-Hua Tan

Open access · hybridAbstract read
In one paragraph

Article in FASEB journal : official publication of the Federation of American Societies for Experimental Biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 26 citations in OpenAlex.

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  20. MAP4K3/GLK in autoimmune disease, cancer and aging.Journal of biomedical science · 2019
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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

7 authors at 4 institutions in 2 countries.

Huai-Chia ChuangImmunology Research Center, National Health Research Institutes, Zhunan, Taiwan.
Yi-Ming ChenDivision of Allergy, Immunology, and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Ming-Han ChenDivision of Allergy, Immunology, and Rheumatology, Taipei Veterans General Hospital, Taipei, Taiwan.
Wei-Ting HungDivision of Allergy, Immunology, and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan.
Huang-Yu YangDepartment of Medicine, Chang Gung Memorial Hospital, Taoyuan, Taiwan.
Yang-Hao TsengImmunology Research Center, National Health Research Institutes, Zhunan, Taiwan.
Tse-Hua TanImmunology Research Center, National Health Research Institutes, Zhunan, Taiwan.
National Health Research Institutes · TWTaichung Veterans General Hospital · TWChang Gung Memorial Hospital · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The cytokine IL-17A plays critical roles in the pathogenesis of autoimmune diseases. The frequencies of MAP kinase kinase kinase kinase 3 [also named germinal center kinase-like kinase (GLK)]-overexpressing T cells are correlated with disease severity of systemic lupus erythematosus (SLE). T-cell-specific GLK-transgenic mice develop spontaneous autoimmune responses through IL-17A. GLK signaling selectively stimulates IL-17A production in murine T cells through inducing aryl hydrocarbon receptor (AhR)-retinoic acid receptor-related orphan nuclear receptor-γt (ROR-γt) complex formation. Here, we investigated whether GLK-induced AhR-ROR-γt complex in T cells is a therapeutic target for human SLE. The population of GLK

Indexed as

AdultAnimalsAutoimmune DiseasesAutoimmunityCytokinesFemaleFlow CytometryHumansInterleukin-17Lupus Erythematosus, SystemicMaleMiceMice, Inbred C57BLNuclear Receptor Subfamily 1, Group F, Member 3PhosphorylationProtein KinasesCytokinesGCK-like kinaseIL17A protein, humanInterleukin-17MAP4K3 protein, humanNuclear Receptor Subfamily 1, Group F, Member 3Protein KinasesProtein Serine-Threonine KinasesReceptors, Aryl HydrocarbonReceptors, Retinoic Acidautoimmune diseaseSLEverteporfin

Identifiers

PMID31318609
PMCPMC6766655
OpenAlexW2962400911

What OpenQuestion holds

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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.