Evidence map›Paper›PMID 19018532›Full record

ArticleCancer immunology, immunotherapy : CII2009

Peroxisome proliferator-activated receptor gamma overexpression and knockdown: impact on human B cell lymphoma proliferation and survival.

Tatiana M Garcia-Bates, Scott A Peslak, Carolyn J Baglole, Sanjay B Maggirwar, Steven H Bernstein, Richard P Phipps

Open access · greenAbstract read
In one paragraph

Article in Cancer immunology, immunotherapy : CII, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Mechanisms underlying the association between obesity and Hodgkin lymphoma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2016
    Review
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  6. Review
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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

6 authors at 1 institution in 1 country.

Tatiana M Garcia-BatesDepartment of Microbiology and Immunology, School of Medicine and Dentistry, University of Rochester, 601 Elmwood Avenue, Rochester, NY 14642, USA.
Scott A Peslak
Carolyn J Baglole
Sanjay B Maggirwar
Steven H Bernstein
Richard P Phipps
University of Rochester · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · NIEHS · UNIVERSITY OF ROCHESTER · PI Martha Susiarjo · 1985 to 2026
$42.8M
REGULATION OF IMMUNITY BY PROSTAGLANDINSR01DE011390 · NIDCR · UNIVERSITY OF ROCHESTER · PI PHIPPS, RICHARD P. · 1994 to 2009
$2.7M
HEMATOLOGY RESEARCHT32HL007152 · NHLBI · UNIVERSITY OF ROCHESTER · PI FRANCIS, CHARLES W. · 1985 to 2011
$2.1M
NHLBI NIH HHS T32 HL007152NHLBI NIH HHS T32HL007152NIDCR NIH HHS DE11390NIDCR NIH HHS R01 DE011390NIEHS NIH HHS ES01247NIEHS NIH HHS P30 ES001247
6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor gamma (PPARgamma) is a multifunctional transcription factor that regulates adipogenesis, immunity and inflammation. Our laboratory previously demonstrated that PPARgamma ligands induce apoptosis in malignant B cells. While malignant B lineage cells such as B cell lymphoma express PPARgamma, its physiological function remains unknown. Herein, we demonstrate that silencing PPARgamma expression by RNAi in human Burkitt's type B lymphoma cells increased basal and mitogen-induced proliferation and survival, which was accompanied by enhanced NF-kappaB activity and increased expression of Bcl-2. These cells also had increased survival upon exposure to PPARgamma ligands and exhibited a less differentiated phenotype. In contrast, PPARgamma overexpression in B lymphoma cells inhibited cell growth and decreased their proliferative response to mitogenic stimuli. These cells were also more sensitive to PPARgamma-ligand induced growth arrest and displayed a more differentiated phenotype. Collectively, these findings support a regulatory role for PPARgamma in the proliferation, survival and differentiation of malignant B cells. These findings further suggest the potential of PPARgamma as a therapeutic target for B cell malignancy.

Indexed as

Burkitt LymphomaCell Line, TumorCell ProliferationCell SurvivalGene Knockdown TechniquesGenetic VectorsHumansLigandsNF-kappa BPAX5 Transcription FactorPositive Regulatory Domain I-Binding Factor 1PPAR gammaProto-Oncogene Proteins c-bcl-2Repressor ProteinsRNA InterferenceLigandsNF-kappa BPAX5 protein, humanPAX5 Transcription FactorPositive Regulatory Domain I-Binding Factor 1PPAR gammaPRDM1 protein, humanProto-Oncogene Proteins c-bcl-2Repressor Proteins

Identifiers

PMID19018532
PMCPMC3003604
OpenAlexW1985810424

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.