Evidence map›Paper›PMID 32655828›Full record

ArticleAmerican journal of translational research2020

The role of adipocytokines and their receptors in bladder cancer: expression of adiponectin or leptin is an independent prognosticator.

Eiji Kashiwagi, Tatsuro Abe, Fumio Kinoshita, Miho Ushijima, Hiroyuki Masaoka, Masaki Shiota, George J Netto, Masatoshi Eto, Hiroshi Miyamoto

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.3field-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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  12. [Correlation between adipokine and clinicopathological features and prognosis in upper tract urothelial carcinoma].Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2022
    Article
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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 2 institutions in 2 countries.

Eiji KashiwagiDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
Tatsuro AbeDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
Fumio KinoshitaDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
Miho UshijimaDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
Hiroyuki MasaokaDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
Masaki ShiotaDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
George J NettoDepartment of Pathology and James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine Baltimore, MD 21287, USA.
Masatoshi EtoDepartment of Urology, Kyushu University Graduate School of Medical Sciences Fukuoka 8128582, Japan.
Hiroshi MiyamotoDepartment of Pathology and James Buchanan Brady Urological Institute, Johns Hopkins University School of Medicine Baltimore, MD 21287, USA.
Kyushu University · JPJohns Hopkins University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adipocytokines such as leptin and adiponectin have functions in metabolism as well as the development and progression of various types of malignancies. However, little is known about their role in bladder cancer. In this study, we investigated whether leptin, adiponectin, and their receptors have an impact on bladder cancer outgrowth and the mechanisms involved. We performed immunohistochemistry for leptin, leptin receptor (Ob-R), adiponectin, and adiponectin receptors (AdipoR1, AdipoR2) in bladder cancer tissue microarrays. Wound healing assay and western blot were then performed in human bladder cancer lines. The positive rates (0 vs 1+/2+/3+) of Ob-R (P=0.004), adiponectin (P<0.001), AdipoR1 (P=0.016), and AdipoR2 (P<0.001) expression were significantly higher in bladder tumors than in benign urothelial tissues. Strong (3+) leptin expression tended to be present more often in tumors (10.2%; P=0.079) than in benign tissues (3.2%). Multivariate analysis revealed a lower risk of recurrence (hazard ratio [HR]=0.432; 95% confidence interval [CI]=0.198-0.942; P=0.034) in patients with an adiponectin-positive non-muscle-invasive tumor and a higher risk of progression (HR=5.148, 95% CI=1.190-22.273; P=0.028) in patients with a leptin-positive muscle-invasive tumor. Treatment of two bladder cancer cell lines with a synthetic adiponectin inhibited their migration and the expressions of phospho-NF-κB, NF-κB, snail, slug, Y-box-binding protein 1, and COX-2, whereas leptin showed reverse effects. Downregulation of adiponectin expression and upregulation of leptin expression were independent predictors for the recurrence of non-muscle-invasive bladder tumors and progression of muscle-invasive bladder tumors, respectively. In summary, synthetic adiponectin might exhibit antitumor activity against bladder cancer.

Indexed as

adiponectinBladder cancerepithelial-to-mesenchymal transitionimmunohistochemistryleptin

Identifiers

PMID32655828
PMCPMC7344091
OpenAlexW3042882552

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.