Evidence map›Paper›PMID 27483249›Full record

ArticleInternational journal of molecular sciences2016

Peroxisome Proliferator-Activated Receptor γ Expression Is Inversely Associated with Macroscopic Vascular Invasion in Human Hepatocellular Carcinoma.

Hui-Tzu Hsu, Ming-Ta Sung, Chih-Chun Lee, Yin-Ju Kuo, Chin-Wen Chi, Hsin-Chen Lee, Cheng-Yuan Hsia

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

19 citing papers in PubMed, 25 citations in OpenAlex.

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  16. The Model ofPPAR research · 2020
    Article
  17. Relationship ofOncoTargets and therapy · 2018
    Article
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  19. 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

7 authors at 2 institutions in 1 country.

Hui-Tzu HsuDepartment and Institute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan. sky7486m@gmail.com.
Ming-Ta SungDepartment of Medical Research, Taipei Veterans General Hospital, Taipei 112, Taiwan. sungmd@gmail.com.
Chih-Chun LeeDepartment and Institute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan. philamo@gmail.com.
Yin-Ju KuoDepartment of Pathology, Taipei Veterans General Hospital, Taipei 112, Taiwan. yjkuo2@vghtpe.gov.tw.
Chin-Wen ChiDepartment and Institute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan. chinwenchi@gmail.com.
Hsin-Chen LeeDepartment and Institute of Pharmacology, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan. hclee2@ym.edu.tw.
Cheng-Yuan HsiaFaculty of Medicine, School of Medicine, National Yang-Ming University, Taipei 112, Taiwan. cyhsia@vghtpe.gov.tw.
National Yang Ming Chiao Tung University · TWTaipei Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor γ (PPARγ) is a ligand-activated nuclear receptor that regulates cellular lipid and glucose metabolism and also plays an inhibitory role in various cancers. However, the role of PPARγ in hepatocellular carcinoma (HCC) remains controversial. This study aimed to investigate the prognostic value of PPARγ in HCC and its role in inhibiting tumor progression, namely, HCC cell growth, migration, and angiogenesis. Immunohistochemical PPARγ staining was examined in 83 HCC specimens to investigate the clinicopathological correlations between PPARγ expression and various parameters. The functional role of PPARγ was determined via PPARγ overexpression and knockdown in HCC cells. Patients with low HCC tissue PPARγ expression were significantly younger (p = 0.006), and exhibited more tumor numbers (p = 0.038), more macroscopic vascular invasion (MVI) (p = 0.008), and more advanced TNM (size of primary tumor, number of regional lymph nodes, and distant metastasis) stages at diagnosis (p = 0.013) than patients with high HCC tissue PPARγ expression. PPARγ knockdown increased HCC cell growth, migration, and angiogenesis, while PPARγ overexpression reduced HCC cell growth, migration, and angiogenesis. These results suggest that low PPARγ expression is an independent predictor of more MVI in HCC patients. PPARγ contributes to the suppression of HCC cell growth, migration, and angiogenesis. Therefore, PPARγ may be a therapeutic target in HCC patients.

Indexed as

AdultAgedAged, 80 and overApoptosisBiomarkers, TumorBlotting, WesternCarcinoma, HepatocellularCell MovementCell ProliferationFemaleHumansImmunoenzyme TechniquesLiver NeoplasmsMaleMiddle AgedNeoplasm InvasivenessBiomarkers, TumorPPAR gammaRNA, Small Interferinghepatocellular carcinomamacroscopic vascular invasionPPARγ

Identifiers

PMID27483249
PMCPMC5000624
OpenAlexW2504215212

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.