Evidence map›Paper›PMID 26869992›Full record

ArticleFrontiers in endocrinology2016

Fenofibrate Induces Ketone Body Production in Melanoma and Glioblastoma Cells.

Maja M Grabacka, Anna Wilk, Anna Antonczyk, Paula Banks, Emilia Walczyk-Tytko, Matthew Dean, Malgorzata Pierzchalska, Krzysztof Reiss

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

30 citing papers in PubMed, 41 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 3 institutions in 2 countries.

Maja M GrabackaDepartment of Food Biotechnology, Faculty of Food Technology, University of Agriculture , Krakow , Poland.
Anna WilkMolecular and Metabolic Oncology Program, Department of Oncologic Sciences, Mitchell Cancer Institute, University of South Alabama , Mobile, AL , USA.
Anna AntonczykDepartment of Food Biotechnology, Faculty of Food Technology, University of Agriculture , Krakow , Poland.
Paula BanksDepartment of Human Nutrition, Faculty of Food Technology, University of Agriculture , Krakow , Poland.
Emilia Walczyk-TytkoDepartment of Food Biotechnology, Faculty of Food Technology, University of Agriculture , Krakow , Poland.
Matthew DeanNeurological Cancer Research, Stanley S Scott Cancer Center, Louisiana State University Health Sciences Center , New Orleans, LA , USA.
Malgorzata PierzchalskaDepartment of Food Biotechnology, Faculty of Food Technology, University of Agriculture , Krakow , Poland.
Krzysztof ReissNeurological Cancer Research, Stanley S Scott Cancer Center, Louisiana State University Health Sciences Center , New Orleans, LA , USA.
University of Agriculture in Krakow · PLLouisiana State University Health Sciences Center New Orleans · USUniversity of South Alabama · US

Funding

Mentoring Translational Researchers in LouisianaP20GM103501 · NIGMS · LSU HEALTH SCIENCES CENTER · PI OCHOA, AUGUSTO C. · 2012 to 2014
$6.3M
Nuclear IRS-1-DNA repair and mutagenesis in medulloblastomaR01CA095518 · NCI · TEMPLE UNIV OF THE COMMONWEALTH · PI REISS, KRZYSZTOF · 2002 to 2012
$2.6M
NCI NIH HHS R01 CA095518NIGMS NIH HHS P20 GM103501
6 · The paper itself

Abstract

Ketone bodies [beta-hydroxybutyrate (bHB) and acetoacetate] are mainly produced in the liver during prolonged fasting or starvation. bHB is a very efficient energy substrate for sustaining ATP production in peripheral tissues; importantly, its consumption is preferred over glucose. However, the majority of malignant cells, particularly cancer cells of neuroectodermal origin such as glioblastoma, are not able to use ketone bodies as a source of energy. Here, we report a novel observation that fenofibrate, a synthetic peroxisome proliferator-activated receptor alpha (PPARa) agonist, induces bHB production in melanoma and glioblastoma cells, as well as in neurospheres composed of non-transformed cells. Unexpectedly, this effect is not dependent on PPARa activity or its expression level. The fenofibrate-induced ketogenesis is accompanied by growth arrest and downregulation of transketolase, but the NADP/NADPH and GSH/GSSG ratios remain unaffected. Our results reveal a new, intriguing aspect of cancer cell biology and highlight the benefits of fenofibrate as a supplement to both canonical and dietary (ketogenic) therapeutic approaches against glioblastoma.

Indexed as

3-hydroxy-3-methylglutaryl-CoA synthetase 2beta-hydroxybutyrateperoxisome proliferator-activated receptor alphatransketolase

Identifiers

PMID26869992
PMCPMC4735548
OpenAlexW2310597351

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.