Evidence map›Paper›PMID 40583347›Full record

ReviewExpert reviews in molecular medicine2025

SIGIRR: An Orphan Receptor Mediating Anti-inflammatory Actions.

Siqi Cheng, Lingyue Cui, Jingyi Chen, Qianwei Xiu, Rujia Si, Xiaoguang Yang, Ying Shi

Abstract readReview
In one paragraph

Review in Expert reviews in molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

7 authors.

Siqi ChengDepartment of Hepatology, First Hospital of Jilin University, Changchun, Jilin, P.R. China.
Lingyue CuiNational Engineering Laboratory for Druggable Gene and Protein Screening, https://ror.org/02rkvz144Northeast Normal University, Changchun, Jilin, P.R. China.
Jingyi ChenClinical Medical College of Jilin University, Changchun, Jilin, P.R. China.
Qianwei XiuDepartment of Hepatology, First Hospital of Jilin University, Changchun, Jilin, P.R. China.
Rujia SiThe Affiliated Cancer Hospital of Nanjing Medical University, Jiangsu Cancer Hospital and Jiangsu Institute of Cancer Research, NanjingChina.
Xiaoguang YangNational Engineering Laboratory for Druggable Gene and Protein Screening, https://ror.org/02rkvz144Northeast Normal University, Changchun, Jilin, P.R. China.
Ying ShiDepartment of Hepatology, First Hospital of Jilin University, Changchun, Jilin, P.R. China.ORCID 0000-0002-4091-0573

Funding

Innovative Research Group Project of the National Natural Science Foundation of China 82270628
6 · The paper itself

Abstract

SIGIRR, also known as the single immunoglobulin interleukin-1 receptor (IL-1R)-related molecule, is a member of the IL-1 receptor superfamily and is believed to play a pivotal role in inflammation and anti-inflammatory regulation within the body. Studies have shown that SIGIRR expression is associated with autoimmunity, inflammatory disorders, graft rejection, viral infection, thrombosis and tumour progression. Due to its unique structure and function, SIGIRR is commonly referred to as an 'orphan receptor', with IL-37 being the only confirmed ligand molecule for SIGIRR to date. The primary mechanism through which SIGIRR exerts its anti-inflammatory regulatory effect involves the negative modulation of the Toll-like receptor-IL-1R (TLR-IL-1R) signalling pathway. TLR-IL-1R signalling plays critical roles in immune responses triggered by microbial invasion and alterations in the tumour immune microenvironment. This article provides an overview of research findings on SIGIRR as an orphan receptor and its regulatory role in maintaining a delicate balance between natural immune activation and uncontrolled inflammatory processes under pathological conditions.

Indexed as

InflammationReceptors, Interleukin-1AnimalsHumansSignal TransductionToll-Like ReceptorsReceptors, Interleukin-1SIGIRR protein, humanToll-Like Receptorsanti-inflammatoryIL-1Rinterleukin-1SIGIRRTLRs

Identifiers

PMID40583347
PMCPMC12315662

What Socratic 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 Socratic graph.