Evidence map›Paper›PMID 33920631›Full record

ArticleInternational journal of molecular sciences2021

SH3BP2 Deficiency Ameliorates Murine Systemic Lupus Erythematosus.

Kyoko Kawahara, Tomoyuki Mukai, Masanori Iseki, Akiko Nagasu, Hajime Nagasu, Takahiko Akagi, Shoko Tsuji, Sumie Hiramatsu-Asano, Yasuyoshi Ueki, Katsuhiko Ishihara and 2 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
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  6. Effect of microRNA-663b on migration, invasion and epithelial‑mesenchymal transition of oral squamous cell carcinoma cells.Hua xi kou qiang yi xue za zhi = Huaxi kouqiang yixue zazhi = West China journal of stomatology · 2022
    Article
  7. TRAPS mutations inFrontiers in immunology · 2022
    Article
  8. Review
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

12 authors at 2 institutions in 2 countries.

Kyoko KawaharaDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Tomoyuki MukaiDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.ORCID 0000-0002-0103-1621
Masanori IsekiDepartment of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Akiko NagasuDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Hajime NagasuDepartment of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Takahiko AkagiDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.ORCID 0000-0003-4055-3083
Shoko TsujiDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Sumie Hiramatsu-AsanoDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.ORCID 0000-0003-2653-9592
Yasuyoshi UekiDepartment of Biomedical Sciences and Comprehensive Care, Indiana University School of Dentistry, Indianapolis, IN 46202, USA.
Katsuhiko IshiharaDepartment of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki 701-0192, Japan.ORCID 0000-0002-2826-5188
Naoki KashiharaDepartment of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Yoshitaka MoritaDepartment of Rheumatology, Kawasaki Medical School, Kurashiki 701-0192, Japan.
Kawasaki Medical School · JPIndiana University School of Medicine

Funding

Foundation for the National Institutes of Health R01DE025870 and R21AR070953GSK Japan Research Grant N.A.Japan Rheumatism foundation N.A.JSPS KAKENHI 18K08398Research Project Grants from Kawasaki Medical School R02G-008, R01B-061, and 30G-005the KAWASAKI Foundation for Medical Science and Medical Welfare N.A.UCB Japan N.A.
6 · The paper itself

Abstract

backgroundThe adaptor protein Src homology 3 domain-binding protein 2 (SH3BP2) is widely expressed in immune cells. It controls intracellular signaling pathways. The present study was undertaken to investigate the role of SH3BP2 in a murine systemic lupus erythematosus model.

methodsFor the lupus model, we used

resultsSH3BP2 deficiency significantly reduced lupus-like phenotypes, presented as splenomegaly, renal involvement, elevated serum anti-dsDNA antibody, and increased splenic B220

conclusionsSH3BP2 deficiency ameliorated lupus-like manifestations. Modulating SH3BP2 expression could thus provide a novel therapeutic approach to autoimmune diseases.

Indexed as

Adaptor Proteins, Signal TransducingAnimalsCell DifferentiationCells, CulturedDendritic CellsFemaleKidneyLupus Erythematosus, SystemicMacrophagesMaleMiceMice, Inbred C57BLSpleenT-LymphocytesAdaptor Proteins, Signal TransducingSh3bp2 protein, mousedendritic cellslupus mouse modelSrc homology 3 domain-binding protein 2systemic lupus erythematosus

Identifiers

PMID33920631
PMCPMC8073120
OpenAlexW3143657578

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.