Evidence map›Paper›PMID 29222347›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2018

Pioglitazone Inhibits Periprostatic White Adipose Tissue Inflammation in Obese Mice.

Miki Miyazawa, Kotha Subbaramaiah, Priya Bhardwaj, Xi Kathy Zhou, Hanhan Wang, Domenick J Falcone, Dilip D Giri, Andrew J Dannenberg

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 20% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Miki MiyazawaDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Kotha SubbaramaiahDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Priya BhardwajDepartment of Medicine, Weill Cornell Medical College, New York, New York.
Xi Kathy ZhouDepartment of Healthcare Policy and Research, Weill Cornell Medical College, New York, New York.
Hanhan WangDepartment of Healthcare Policy and Research, Weill Cornell Medical College, New York, New York.
Domenick J FalconeDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, New York.
Dilip D GiriDepartment of Pathology, Memorial Sloan Kettering Cancer Center, New York, New York.
Andrew J DannenbergDepartment of Medicine, Weill Cornell Medical College, New York, New York. ajdannen@med.cornell.edu.
Cornell University · US

Funding

X-RAY CRYSTALLOGRAPHYP30CA008748 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Nicholas D Socci · 1985 to 2026
$347.4M
SPORE In Prostate CancerP50CA092629 · NCI · SLOAN-KETTERING INSTITUTE FOR CANCER RES · PI Yu Chen, MICHAEL J MORRIS · 2001 to 2026
$63.0M
NCI NIH HHS P30 CA008748NCI NIH HHS P50 CA092629
6 · The paper itself

Abstract

Obesity is associated with an increased incidence of high-grade prostate cancer and poor prognosis for prostate cancer patients. Recently, we showed that obesity-related periprostatic white adipose tissue (WAT) inflammation, characterized by crown-like structures (CLS) consisting of dead or dying adipocytes surrounded by macrophages, was associated with high-grade prostate cancer. It is possible, therefore, that agents that suppress periprostatic WAT inflammation will alter the development or progression of prostate cancer. Pioglitazone, a ligand of PPARγ, is used to treat diabetes and possesses anti-inflammatory properties. Here, our main objectives were to determine whether pioglitazone inhibited obesity-related periprostatic WAT inflammation in mice and then to elucidate the underlying mechanism. Treatment with pioglitazone reduced the density of CLS in periprostatic fat and suppressed levels of TNFα, TGFβ, and the chemokine monocyte chemoattractant protein-1 (MCP-1). Importantly, the ability of pioglitazone to suppress periprostatic WAT inflammation was abrogated in

Indexed as

Adipose Tissue, WhiteAnimalsCells, CulturedChemokine CCL2Diet, High-FatHypoglycemic AgentsInflammationMaleMiceMice, Inbred C57BLMice, KnockoutMice, ObesePioglitazoneProstateChemokine CCL2Hypoglycemic AgentsPioglitazone

Identifiers

PMID29222347
PMCPMC5882568
OpenAlexW2771311308

What OpenQuestion holds

Textmetadata
LicenceTDM
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.