Evidence map›Paper›PMID 24757676›Full record

ArticleBioMed research international2014

Rosiglitazone regulates anti-inflammation and growth inhibition via PTEN.

Chiou-Feng Lin, Kung-Chia Young, Chyi-Huey Bai, Bu-Chin Yu, Ching-Ting Ma, Yu-Chieh Chien, Chiu-Ling Chiang, Chao-Sheng Liao, Hsin-Wen Lai, Chiung-Wen Tsao

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.3field-weighted citation impact, top 21% 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

20 citing papers in PubMed, 33 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

10 authors at 3 institutions in 1 country.

Chiou-Feng LinInstitute of Clinical Medicine, National Cheng Kung University Medical College, Tainan 70101, Taiwan.
Kung-Chia YoungDepartment of Medical Laboratory Science and Biotechnology, National Cheng Kung University Medical College, Tainan 70101, Taiwan.
Chyi-Huey BaiSchool of Public Health, Taipei Medical University, Taipei 11031, Taiwan.
Bu-Chin YuDepartment of Life Sciences, College of Bioscience and Biotechnology, National Cheng Kung University Medical College, Tainan 70101, Taiwan.
Ching-Ting MaInstitute of Clinical Medicine, National Cheng Kung University Medical College, Tainan 70101, Taiwan ; Department of Nursing, Chung Hwa University of Medical Technology, No. 89, Wen-Hwa 1st Street, Jen-Te Hsiang, Tainan 71703, Taiwan.
Yu-Chieh ChienDepartment of Medical Laboratory Science and Biotechnology, National Cheng Kung University Medical College, Tainan 70101, Taiwan ; Department of Nursing, Chung Hwa University of Medical Technology, No. 89, Wen-Hwa 1st Street, Jen-Te Hsiang, Tainan 71703, Taiwan.
Chiu-Ling ChiangDepartment of Nursing, Chung Hwa University of Medical Technology, No. 89, Wen-Hwa 1st Street, Jen-Te Hsiang, Tainan 71703, Taiwan.
Chao-Sheng LiaoDepartment of Gastroenterology, Shin Kong Wu Ho-Su Memorial Hospital, Taipei 11101, Taiwan.
Hsin-Wen LaiDepartment of Gastroenterology, Shin Kong Wu Ho-Su Memorial Hospital, Taipei 11101, Taiwan.
Chiung-Wen TsaoDepartment of Nursing, Chung Hwa University of Medical Technology, No. 89, Wen-Hwa 1st Street, Jen-Te Hsiang, Tainan 71703, Taiwan.
National Cheng Kung University · TWChung Hwa University of Medical Technology · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor gamma (PPARγ) agonist has anti-inflammatory and anticancer properties. However, the mechanisms by which PPARγ agonist rosiglitazone interferes with inflammation and cancer via phosphatase and tensin homolog-(PTEN)-dependent pathway remain unclear. We found that lower doses (<25  μ M) of rosiglitazone significantly inhibited lipopolysaccharide-(LPS)-induced nitric oxide (NO) release (via inducible nitric oxide synthase, iNOS), prostaglandin E2 (PGE2) production (via cyclooxygenase-2, COX-2), and activation of Akt in RAW 264.7 murine macrophages. However, rosiglitazone did not inhibit the production of reactive oxygen species (ROS). In PTEN knockdown (shPTEN) cells exposed to LPS, rosiglitazone did not inhibit NO release, PGE2 production, and activation of Akt. These cells had elevated basal levels of iNOS, COX-2, and ROS. However, higher doses (25-100  μ M) of rosiglitazone, without LPS stimulation, did not block NO release and PGE2 productions, but they inhibited p38 MAPK phosphorylation and blocked ROS generation in shPTEN cells. In addition, rosiglitazone caused G1 arrest and reduced the number of cells in S + G2/M phase, leading to growth inhibition. These results indicate that the anti-inflammatory property of rosiglitazone is related to regulation of PTEN independent of inhibition on ROS production. However, rosiglitazone affected the dependence of PTEN-deficient cell growth on ROS.

Indexed as

AnimalsAnti-Inflammatory Agents, Non-SteroidalCell LineCyclooxygenase 2G1 Phase Cell Cycle CheckpointsHypoglycemic AgentsLipopolysaccharidesMacrophagesMiceNitric OxidePPAR gammaProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseReactive Oxygen SpeciesRosiglitazoneThiazolidinedionesAnti-Inflammatory Agents, Non-SteroidalCyclooxygenase 2Hypoglycemic AgentsLipopolysaccharidesNitric OxidePPAR gammaProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePten protein, mousePtgs2 protein, mouseReactive Oxygen SpeciesRosiglitazoneThiazolidinediones

Identifiers

PMID24757676
PMCPMC3971553
OpenAlexW2070581477

What OpenQuestion holds

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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.