Evidence map›Paper›PMID 30402506›Full record

ReviewJournal of immunology research2018

TNIP1 in Autoimmune Diseases: Regulation of Toll-like Receptor Signaling.

Rambon Shamilov, Brian J Aneskievich

Open access · goldAbstract readReview
In one paragraph

Review in Journal of immunology research, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
2.0field-weighted citation impact, top 10% 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

43 citing papers in PubMed, 70 citations in OpenAlex.

  1. Article
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  11. Investigating Protein-Protein Interactions of Autophagy-Involved TNIP1.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  12. Review
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  18. Review
  19. Repressive Control of Keratinocyte Cytoplasmic Inflammatory Signaling.International journal of molecular sciences · 2023
    Review
  20. Article
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

2 authors at 1 institution in 1 country.

Rambon ShamilovDepartment of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269-3092, USA.ORCID 0000-0003-0375-7482
Brian J AneskievichDepartment of Pharmaceutical Sciences, University of Connecticut, Storrs, CT 06269-3092, USA.ORCID 0000-0001-7440-1948
University of Connecticut · US

Funding

Keratinocyte Nuclear Receptor CoactivatorsR01AR048660 · NIAMS · UNIVERSITY OF CONNECTICUT STORRS · PI ANESKIEVICH, BRIAN J · 2005 to 2009
$1.4M
NIAMS NIH HHS R01 AR048660
6 · The paper itself

Abstract

TNIP1 protein is increasingly being recognized as a key repressor of inflammatory signaling and a potential factor in multiple autoimmune diseases. In addition to earlier foundational reports of TNIP1 SNPs in human autoimmune diseases and TNIP1 protein-protein interaction with receptor regulating proteins, more recent studies have identified new potential interaction partners and signaling pathways likely modulated by TNIP1. Subdomains within the TNIP1 protein as well as how they interact with ubiquitin have not only been mapped but inflammatory cell- and tissue-specific consequences subsequent to their defective function are being recognized and related to human disease states such as lupus, scleroderma, and psoriasis. In this review, we emphasize receptor signaling complexes and regulation of cytoplasmic signaling steps downstream of TLR given their association with some of the same autoimmune diseases where TNIP1 has been implicated. TNIP1 dysfunction or deficiency may predispose healthy cells to the inflammatory response to otherwise innocuous TLR ligand exposure. The recognition of the anti-inflammatory roles of TNIP1 and improved integrated understanding of its physical and functional association with other signaling pathway proteins may position TNIP1 as a candidate target for the design and/or testing of next-generation anti-inflammatory therapeutics.

Indexed as

Autoimmune DiseasesDNA-Binding ProteinsGenetic Predisposition to DiseaseHumansInflammationPolymorphism, GeneticSignal TransductionToll-Like ReceptorsDNA-Binding ProteinsTNIP1 protein, humanToll-Like Receptors

Identifiers

PMID30402506
PMCPMC6192141
OpenAlexW2895574251

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.