Evidence map›Paper›PMID 24409188›Full record

ReviewFrontiers in immunology2014

Thioredoxin/Txnip: redoxisome, as a redox switch for the pathogenesis of diseases.

Eiji Yoshihara, So Masaki, Yoshiyuki Matsuo, Zhe Chen, Hai Tian, Junji Yodoi

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 206 papers.

0numbers the graph read from it
0cells of the map it votes in
206citing papers in PubMed
11.1field-weighted citation impact, top 1% 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

206 citing papers in PubMed, 353 citations in OpenAlex.

  1. Review
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  7. Loss of Peroxiredoxin 6 Drives Age-Related Klf9/NF-Antioxidants (Basel, Switzerland) · 2026
    Article
  8. International journal of molecular sciences · 2026
    Article
  9. Review
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146 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Eiji YoshiharaInstitute for Virus Research, Kyoto University , Kyoto , Japan.
So MasakiInstitute for Virus Research, Kyoto University , Kyoto , Japan.
Yoshiyuki MatsuoInstitute for Virus Research, Kyoto University , Kyoto , Japan.
Zhe ChenInstitute for Virus Research, Kyoto University , Kyoto , Japan.
Hai TianAdvanced Chemical Technology Center in Kyoto (ACT Kyoto), JBPA Research Institute , Kyoto , Japan ; Redox Bio Science Inc. , Kyoto , Japan.
Junji YodoiInstitute for Virus Research, Kyoto University , Kyoto , Japan ; Advanced Chemical Technology Center in Kyoto (ACT Kyoto), JBPA Research Institute , Kyoto , Japan ; Redox Bio Science Inc. , Kyoto , Japan.
Kyoto University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the past few decades, it has been widely recognized that Reduction-Oxidation (redox) responses occurring at the intra- and extra-cellular levels are one of most important biological phenomena and dysregulated redox responses are involved in the initiation and progression of multiple diseases. Thioredoxin1 (Trx1) and Thioredoxin2 (Trx2), mainly located in the cytoplasm and mitochondria, respectively, are ubiquitously expressed in variety of cells and control cellular reactive oxygen species by reducing the disulfides into thiol groups. Thioredoxin interacting protein (Txnip/thioredoxin binding protein-2/vitamin D3 upregulated protein) directly binds to Trx1 and Trx2 (Trx) and inhibit the reducing activity of Trx through their disulfide exchange. Recent studies have revealed that Trx1 and Txnip are involved in some critical redox-dependent signal pathways including NLRP-3 inflammasome activation in a redox-dependent manner. Therefore, Trx/Txnip, a redox-sensitive signaling complex is a regulator of cellular redox status and has emerged as a key component in the link between redox regulation and the pathogenesis of diseases. Here, we review the novel functional concept of the redox-related protein complex, named "Redoxisome," consisting of Trx/Txnip, as a critical regulator for intra- and extra-cellular redox signaling, involved in the pathogenesis of various diseases such as cancer, autoimmune disease, and diabetes.

Indexed as

diabetes mellitusinflammationredoxisomeredox regulationthioredoxinTxnip

Identifiers

PMID24409188
PMCPMC3885921
OpenAlexW1995762247

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.