Evidence map›Paper›PMID 25950488›Full record

ArticleCell death & disease2015

IPS-1 differentially induces TRAIL, BCL2, BIRC3 and PRKCE in type I interferons-dependent and -independent anticancer activity.

S Kumar, H Ingle, S Mishra, R S Mahla, A Kumar, T Kawai, S Akira, A Takaoka, A A Raut, H Kumar

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

31 citing papers in PubMed, 48 citations in OpenAlex.

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  15. Dll1Nature communications · 2021
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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

10 authors at 5 institutions in 2 countries.

S KumarLaboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India.
H IngleLaboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India.
S MishraLaboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India.
R S MahlaLaboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India.
A KumarLaboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India.
T KawaiLaboratory of Molecular Immunobiology, Graduate School of Biological Sciences, Nara Institute of Science and Technology, Nara, Japan.
S AkiraLaboratory of Host Defense, WPI Immunology Frontier Research Centre, Osaka University, Osaka, Japan.
A TakaokaDivision of Signaling in Cancer and Immunology, Institute for Genetic Medicine, Hokkaido University, Sapporo, Japan.
A A RautPathogenomics Laboratory, ICAR-National Institute of High Security Animal Diseases, OIE Reference lab for Avian Influenza, Bhopal, India.
H Kumar1] Laboratory of Immunology, Department of Biological Sciences, Indian Institute of Science Education and Research, Bhopal, India [2] Laboratory of Host Defense, WPI Immunology Frontier Research Centre, Osaka University, Osaka, Japan.
Indian Institute of Science Education and Research, Bhopal · INOsaka University · JPHokkaido University · JPNara Institute of Science and Technology · JPNational Institute of High Security Animal Diseases · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

RIG-I-like receptors are the key cytosolic sensors for RNA viruses and induce the production of type I interferons (IFN) and pro-inflammatory cytokines through a sole adaptor IFN-β promoter stimulator-1 (IPS-1) (also known as Cardif, MAVS and VISA) in antiviral innate immunity. These sensors also have a pivotal role in anticancer activity through induction of apoptosis. However, the mechanism for their anticancer activity is poorly understood. Here, we show that anticancer vaccine adjuvant, PolyIC (primarily sensed by MDA5) and the oncolytic virus, Newcastle disease virus (NDV) (sensed by RIG-I), induce anticancer activity. The ectopic expression of IPS-1 into type I IFN-responsive and non-responsive cancer cells induces anticancer activity. PolyIC transfection and NDV infection upregulate pro-apoptotic gene TRAIL and downregulate the anti-apoptotic genes BCL2, BIRC3 and PRKCE. Furthermore, stable knockdown of IPS-1, IRF3 or IRF7 in IFN-non-responsive cancer cells show reduced anticancer activity by suppressing apoptosis via TRAIL and anti-apoptotic genes. Collectively, our study shows that IPS-1 induces anticancer activity through upregulation of pro-apoptotic gene TRAIL and downregulation of the anti-apoptotic genes BCL2, BIRC3 and PRKCE via IRF3 and IRF7 in type I IFN-dependent and -independent manners.

Indexed as

Adaptor Proteins, Signal TransducingApoptosisBaculoviral IAP Repeat-Containing 3 ProteinCancer VaccinesCell Line, TumorDown-RegulationHEK293 CellsHumansInhibitor of Apoptosis ProteinsInterferon Regulatory Factor-3Interferon Regulatory Factor-7Interferon Type INeoplasm InvasivenessNeoplasmsNewcastle disease virusPoly I-CAdaptor Proteins, Signal TransducingBaculoviral IAP Repeat-Containing 3 ProteinBCL2 protein, humanBIRC3 protein, humanCancer VaccinesInhibitor of Apoptosis ProteinsInterferon Regulatory Factor-3Interferon Regulatory Factor-7Interferon Type IIRF3 protein, humanIRF7 protein, humanMAVS protein, humanPoly I-CPRKCE protein, humanProtein Kinase C-epsilonProto-Oncogene Proteins c-bcl-2RNA, Small InterferingTNF-Related Apoptosis-Inducing LigandTNFSF10 protein, humanUbiquitin-Protein Ligases

Identifiers

PMID25950488
PMCPMC4669701
OpenAlexW1498684083

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.