Evidence map›Paper›PMID 29496994›Full record

ArticleThe Journal of biological chemistry2018

Fascin1 suppresses RIG-I-like receptor signaling and interferon-β production by associating with IκB kinase ϵ (IKKϵ) in colon cancer.

Tomio Matsumura, Shigeaki Hida, Masato Kitazawa, Chifumi Fujii, Akira Kobayashi, Michiko Takeoka, Shun-Ichiro Taniguchi, Shin-Ichi Miyagawa

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
0.9field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 21 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

8 authors at 3 institutions in 2 countries.

Tomio MatsumuraFrom the Departments of Molecular Oncology and.
Shigeaki Hidathe Department of Molecular and Cellular Health Science, Nagoya University Graduate School of Pharmaceutical Sciences, Nagoya 467-8603, Japan hida@phar.nagoya-cu.ac.jp.
Masato Kitazawathe Department of Surgery, Shinshu University School of Medicine, and.
Chifumi FujiiFrom the Departments of Molecular Oncology and.
Akira Kobayashithe Department of Surgery, Shinshu University School of Medicine, and.
Michiko Takeokathe Department of Surgery, Shinshu University School of Medicine, and.
Shun-Ichiro TaniguchiFrom the Departments of Molecular Oncology and.
Shin-Ichi Miyagawathe Department of Surgery, Shinshu University School of Medicine, and shinichi@shinshu-u.ac.jp.
Shinshu University · JPMolecular Oncology (United States) · USNagoya University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fascin1 is an actin-bundling protein involved in cancer cell migration and has recently been shown also to have roles in virus-mediated immune cell responses. Because viral infection has been shown to activate immune cells and to induce interferon-β expression in human cancer cells, we evaluated the effects of fascin1 on virus-dependent signaling via the membrane- and actin-associated protein RIG-I (retinoic acid-inducible gene I) in colon cancer cells. We knocked down fascin1 expression with shRNA retrovirally transduced into a DLD-1 colon cancer and L929 fibroblast-like cell lines and used luciferase reporter assays and co-immunoprecipitation to identify fascin1 targets. We found that intracellular poly(I·C) transfection to mimic viral infection enhances the RIG-I/MDA5 (melanoma differentiation-associated gene 5)-mediated dimerization of interferon regulatory factor 3 (IRF-3). The transfection also significantly increased the expression levels of IRF-7, interferon-β, and interferon-inducible cytokine IP-10 in fascin1-deleted cells compared with controls while significantly suppressing cell growth, migration, and invasion. We also found that fascin1 constitutively interacts with IκB kinase ϵ (IKKϵ) in the RIG-I signaling pathway. In summary, we have identified fascin1 as a suppressor of the RIG-I signaling pathway associating with IκB kinase ϵ in DLD-1 colon cancer cells to suppress immune responses to viral infection.

Indexed as

Signal TransductionAnimalsCarrier ProteinsCell Line, TumorColonic NeoplasmsDEAD Box Protein 58HEK293 CellsHumansI-kappa B KinaseInterferon-betaMiceMicrofilament ProteinsNeoplasm ProteinsReceptors, ImmunologicVirus DiseasesCarrier ProteinsDEAD Box Protein 58FSCN1 protein, humanI-kappa B KinaseInterferon-betaMicrofilament ProteinsNeoplasm ProteinsReceptors, ImmunologicRIGI protein, humaninterferoninterferon regulatory factor (IRF)invasionIκB Kinase ϵ fascin1poly(I·C)RIG-I-like receptor (RLR)signal transducers and activators of transcription 1 (STAT1)

Identifiers

PMID29496994
PMCPMC5925820
OpenAlexW2790099812

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.