Evidence map›Paper›PMID 26740747›Full record

ReviewClinical medicine insights. Circulatory, respiratory and pulmonary medicine2015

Myriad Functions of Stanniocalcin-1 (STC1) Cover Multiple Therapeutic Targets in the Complicated Pathogenesis of Idiopathic Pulmonary Fibrosis (IPF).

Shinya Ohkouchi, Manabu Ono, Makoto Kobayashi, Taizou Hirano, Yutaka Tojo, Shu Hisata, Masakazu Ichinose, Toshiya Irokawa, Hiromasa Ogawa, Hajime Kurosawa

Open access · goldAbstract readReview
In one paragraph

Review in Clinical medicine insights. Circulatory, respiratory and pulmonary medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.2field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Review
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  9. Article
  10. Review
  11. Expression, function and clinical application of stanniocalcin-1 in cancer.Journal of cellular and molecular medicine · 2020
    Review
  12. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Current Developments in Interstitial Lung Disease.Clinical medicine insights. Circulatory, respiratory and pulmonary medicine · 2015
    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

10 authors at 2 institutions in 2 countries.

Shinya OhkouchiDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan; Department of Occupational Health, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Manabu OnoDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Makoto KobayashiDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Taizou HiranoDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Yutaka TojoDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Shu HisataDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan; Joan and Sanford I. Weill Department of Medicine, Weill Cornell Medical College and New York-Presbyterian Hospital, New York, NY, USA; Division of Pulmonary and Critical Care Medicine, Weill Cornell Medical College, New York, NY, USA.
Masakazu IchinoseDepartment of Respiratory Medicine, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Toshiya IrokawaDepartment of Occupational Health, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Hiromasa OgawaDepartment of Occupational Health, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Hajime KurosawaDepartment of Occupational Health, Graduate School of Medicine, Tohoku University, Sendai, Japan.
Tohoku University · JPNew York Hospital Queens · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary fibrosis (IPF) is an intractable disease for which the pathological findings are characterized by temporal and spatial heterogeneity. The pathogenesis is composed of myriad factors, including repetitive injuries to epithelial cells, alterations in immunity, the formation of vascular leakage and coagulation, abnormal wound healing, fibrogenesis, and collagen accumulation. Therefore, the molecular target drugs that are used or attempted for treatment or clinical trials may not cover the myriad therapeutic targets of IPF. In addition, the complicated pathogenesis results in a lack of informative biomarkers to diagnose accurately the status of IPF. These facts point out the necessity of using a combination of drugs, that is, each single drug with molecular targets or a single drug with multiple therapeutic targets. In this review, we introduce a humoral factor, stanniocalcin-1 (STC1), which has myriad functions, including the maintenance of calcium homeostasis, the promotion of early wound healing, uncoupling respiration (aerobic glycolysis), reepithelialization in damaged tissues, the inhibition of vascular leakage, and the regulation of macrophage functions to keep epithelial and endothelial homeostasis, which may adequately cover the myriad therapeutic targets of IPF.

Indexed as

biomarkeridiopathic pulmonary fibrosis (IPF)macrophagestanniocalcin-1 (STC1)wound healing

Identifiers

PMID26740747
PMCPMC4696838
OpenAlexW2197660167

What OpenQuestion holds

Textmetadata
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.