Evidence mapPaperPMID 20204067Full record

ArticlePPAR research2010

Anticancer Role of PPARgamma Agonists in Hematological Malignancies Found in the Vasculature, Marrow, and Eyes.

P J Simpson-Haidaris, S J Pollock, S Ramon, N Guo, C F Woeller, S E Feldon, R P Phipps

Open access · goldAbstract read
In one paragraph

Article in PPAR research, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 15 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

7 authors at 1 institution in 1 country.

P J Simpson-HaidarisDepartment of Medicine/Hem-Onc Division, School of Medicine and Dentistry, University of Rochester, Rochester, NY 14642, USA.
S J Pollock
S Ramon
N Guo
C F Woeller
S E Feldon
R P Phipps
University of Rochester · US

Funding

VISUAL INDICES OF NEUROTOXICITYP30ES001247 · UNIVERSITY OF ROCHESTER · 1985 to 2025
$10.5M
ORAL CELLULAR AND MOLECULAR BIOLOGY TRAINING GRANTT32DE007202 · UNIVERSITY OF ROCHESTER · 1990 to 2005
$2.0M
REGULATION OF IMMUNITY BY PROSTAGLANDINSR01DE011390 · UNIVERSITY OF ROCHESTER · 1994 to 2005
$1.3M
Platelet Activation and Inflammatory MediatorsR01HL078603 · UNIVERSITY OF ROCHESTER · 2004 to 2005
$624k
NEI NIH HHS R01 EY017123NHLBI NIH HHS R01 HL078603NIDCR NIH HHS R01 DE011390NIDCR NIH HHS T32 DE007202NIDCR NIH HHS T90 DE021985NIEHS NIH HHS P30 ES001247
6 · The paper itself

Abstract

The use of targeted cancer therapies in combination with conventional chemotherapeutic agents and/or radiation treatment has increased overall survival of cancer patients. However, longer survival is accompanied by increased incidence of comorbidities due, in part, to drug side effects and toxicities. It is well accepted that inflammation and tumorigenesis are linked. Because peroxisome proliferator-activated receptor (PPAR)-gamma agonists are potent mediators of anti-inflammatory responses, it was a logical extension to examine the role of PPARgamma agonists in the treatment and prevention of cancer. This paper has two objectives: first to highlight the potential uses for PPARgamma agonists in anticancer therapy with special emphasis on their role when used as adjuvant or combined therapy in the treatment of hematological malignancies found in the vasculature, marrow, and eyes, and second, to review the potential role PPARgamma and/or its ligands may have in modulating cancer-associated angiogenesis and tumor-stromal microenvironment crosstalk in bone marrow.

Identifiers

PMID20204067
PMCPMC2829627
OpenAlexW2087983787

What Socratic 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 Socratic graph.