Evidence map›Paper›PMID 35456905›Full record

ArticleInternational journal of molecular sciences2022

Possible Repositioning of an Oral Anti-Osteoporotic Drug, Ipriflavone, for Treatment of Inflammatory Arthritis via Inhibitory Activity of KIAA1199, a Novel Potent Hyaluronidase.

Hiroshi Koike, Yoshihiro Nishida, Tamayuki Shinomura, Bisei Ohkawara, Kinji Ohno, Lisheng Zhuo, Koji Kimata, Takahiro Ushida, Shiro Imagama

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.6field-weighted citation impact, top 40% 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

6 citing papers in PubMed, 6 citations in OpenAlex.

  1. Ipriflavone FromMedComm · 2026
    Article
  2. Article
  3. Article
  4. Non-polar components in PMFrontiers in genetics · 2025
    Article
  5. Article
  6. 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

9 authors at 4 institutions in 1 country.

Hiroshi KoikeDepartment of Orthopedic Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya 466-8550, Japan.ORCID 0000-0002-2997-6635
Yoshihiro NishidaDepartment of Rehabilitation Medicine, Nagoya University Hospital, 65 Tsurumai, Showa, Nagoya 466-8550, Japan.
Tamayuki ShinomuraDepartment of Hard Tissue Engineering, Tokyo Medical and Dental University, Tokyo 113-8510, Japan.
Bisei OhkawaraCenter for Neurological Diseases and Cancer, Division of Neurogenetics, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya 466-8550, Japan.ORCID 0000-0002-1987-458X
Kinji OhnoCenter for Neurological Diseases and Cancer, Division of Neurogenetics, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya 466-8550, Japan.ORCID 0000-0002-1529-2750
Lisheng ZhuoDepartment of Orthopedic Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya 466-8550, Japan.
Koji KimataMultidisciplinary Pain Center, Aichi Medical University, Nagakute 480-1195, Japan.
Takahiro UshidaMultidisciplinary Pain Center, Aichi Medical University, Nagakute 480-1195, Japan.
Shiro ImagamaDepartment of Orthopedic Surgery, Nagoya University Graduate School of Medicine, 65 Tsurumai, Showa, Nagoya 466-8550, Japan.
Nagoya University · JPAichi Medical University · JPNagoya University Hospital · JPTokyo Medical and Dental University · JP

Funding

Ministry of Education, Culture, Sports, Science and Technology of Japan 20K18060 for Young Scientists
6 · The paper itself

Abstract

KIAA1199 has a strong hyaluronidase activity in inflammatory arthritis. This study aimed to identify a drug that could reduce KIAA1199 activity and clarify its effects on inflammatory arthritis. Rat chondrosarcoma (RCS) cells were strongly stained with Alcian blue (AB). Its stainability was reduced in RCS cells, which were over-expressed with the KIAA1199 gene (RCS-KIAA). We screened the drugs that restore the AB stainability in RCS-KIAA. The effects of the drug were evaluated by particle exclusion assay, HA ELISA, RT-PCR, and Western blotting. We further evaluated the HA accumulation and the MMP1 and three expressions in fibroblast-like synoviocytes (FLS). In vivo, the effects of the drug on symptoms and serum concentration of HA in a collagen-induced arthritis mouse were evaluated. Ipriflavone was identified to restore AB stainability at 23%. Extracellular matrix formation was significantly increased in a dose-dependent manner (

Indexed as

Arthritis, ExperimentalSynoviocytesAnimalsDrug RepositioningFibroblastsHyaluronic AcidHyaluronoglucosaminidaseIsoflavonesMatrix Metalloproteinase 1MiceRatsHyaluronic AcidHyaluronoglucosaminidaseipriflavoneIsoflavonesMatrix Metalloproteinase 1CEMIPcollagen-induced arthritishyaluronanhyaluronidaseinflammatory arthritisKIAA1199

Identifiers

PMID35456905
PMCPMC9030858
OpenAlexW4224244259

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.