Evidence map›Paper›PMID 21490130›Full record

ArticleCancer prevention research (Philadelphia, Pa.)2011

Dietary fish oil promotes colonic apoptosis and mitochondrial proton leak in oxidatively stressed mice.

Yang-Yi Fan, Qitao Ran, Shinya Toyokuni, Yasumasa Okazaki, Evelyn S Callaway, Joanne R Lupton, Robert S Chapkin

Open access · bronzeAbstract read
In one paragraph

Article in Cancer prevention research (Philadelphia, Pa.), 2011. 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
1.7field-weighted citation impact, top 16% 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, 32 citations in OpenAlex.

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  8. Dietary fat and fiber interactively modulate apoptosis and mitochondrial bioenergetic profiles in mouse colon in a site-specific manner.European journal of cancer prevention : the official journal of the European Cancer Prevention Organisation (ECP) · 2017
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  13. A bioassay to measure energy metabolism in mouse colonic crypts, organoids, and sorted stem cells.American journal of physiology. Gastrointestinal and liver physiology · 2015
    Article
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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 4 institutions in 2 countries.

Yang-Yi FanProgram in Integrative Nutrition & Complex Diseases, Texas A&M University, College Station, TX, USA.
Qitao Ran
Shinya Toyokuni
Yasumasa Okazaki
Evelyn S Callaway
Joanne R Lupton
Robert S Chapkin
Nagoya University · JPThe University of Texas Health Science Center at San Antonio · USCollege Station Medical Center · USTexas A&M University · US

Funding

Pilot--Health Science ResearchP30ES009106 · NIEHS · TEXAS A&M UNIVERSITY SYSTEM · PI SAFE, STEPHEN H. · 1998 to 2006
$9.2M
Colonic Cytokinetics and Cell Signaling: Dietary EffectsR01CA059034 · NCI · TEXAS A&M UNIVERSITY SYSTEM · PI CHAPKIN, ROBERT STEPHEN · 1995 to 2012
$3.6M
Gene expression analysis of coding and non-coding RNAs in colon cancer preventionR01CA129444 · NCI · TEXAS A&M UNIVERSITY · PI CHAPKIN, ROBERT STEPHEN · 2007 to 2015
$2.1M
NCI NIH HHS CA129444NCI NIH HHS CA59034NCI NIH HHS R01 CA059034NCI NIH HHS R01 CA129444NIEHS NIH HHS P30 ES009106NIEHS NIH HHS P30ES09106
6 · The paper itself

Abstract

An alteration of mitochondrial function can result in disruption of redox homeostasis and is associated with abnormal cancer cell growth. Manganese superoxide dismutase (SOD2) and glutathione peroxidase 4 (Gpx4) are two of the most important antioxidant defense enzymes that protect cells against oxidative stress. We had previously shown that n-3 polyunsaturated fatty acids (PUFA) promote colonocyte apoptosis, a marker of colon cancer risk, in part by enhancing phospholipid oxidation. To elucidate the mechanisms regulating oxidative stress-induced apoptosis in vivo, we fed heterozygous SOD2(Het), Gpx4(Het), and transgenic Gpx4(Tg) mice diets containing either 15% corn oil by weight (CO, enriched in n-6 PUFA) or 3.5% CO + 11.5% fish oil (FO, enriched in n-3 PUFA) for 4 weeks. Our data showed that (i) genetic predeposition to oxidative stress facilitates apoptosis in the mouse colon (Gpx4(Het) > SOD2(Het) > Wt > Gpx4(Tg)), (ii) dietary n-3 PUFA have an additive effect on the induction of apoptosis in Gpx4(Het) and SOD2(Het) mice; and (iii) dietary n-3 PUFA reverse the phenotype in oxidatively protected Gpx4(Tg) mice by elevating apoptosis to a level observed in wild-type (Wt; control) animals. Complimentary experiments examining colonic mitochondrial bioenergetic profiles indicate that FO-fed mice exhibit a significantly (P < 0.05) increased respiration-induced proton leak relative to control CO treatment. This finding was consistent with a loss of membrane potential in response to chronic oxidative stress and supports the contention that n-3 PUFA alter mitochondrial metabolic activity, thereby enhancing apoptosis and reducing colon cancer risk.

Indexed as

ApoptosisAnimalsCardiolipinsColonCrosses, GeneticDietary Fats, UnsaturatedFish OilsGenotypeGlutathione PeroxidaseMiceMice, Inbred C57BLMitochondriaOxidative StressOxygen ConsumptionPhospholipid Hydroperoxide Glutathione PeroxidaseProtonsCardiolipinsDietary Fats, UnsaturatedFish OilsGlutathione PeroxidasePhospholipid Hydroperoxide Glutathione PeroxidaseProtons

Identifiers

PMID21490130
PMCPMC3137683
OpenAlexW2122433162

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.