Evidence map›Paper›PMID 32006211›Full record

ReviewDigestive diseases and sciences2020

Diet and Gut Microbes Act Coordinately to Enhance Programmed Cell Death and Reduce Colorectal Cancer Risk.

Robert S Chapkin, Sandi L Navarro, Meredith A J Hullar, Johanna W Lampe

Open access · greenAbstract readReview
In one paragraph

Review in Digestive diseases and sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 3 pooled it
3.0field-weighted citation impact, top 8% 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

36 citing papers in PubMed, 3 syntheses or guidelines pooled it, 56 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

4 authors at 2 institutions in 1 country.

Robert S ChapkinDepartment of Nutrition, Texas A&M University, College Station, TX, USA. r-chapkin@tamu.edu.
Sandi L NavarroPublic Health Sciences Division, and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Meredith A J HullarPublic Health Sciences Division, and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Johanna W LampePublic Health Sciences Division, and Clinical Research Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
Fred Hutch Cancer Center · USTexas A&M University · US

Funding

Plasma membrane therapy: Disruption of Wnt associated receptor spatiotemporal organization by membrane targeted dietary bioactives (MTDB)R35CA197707 · NCI · TEXAS A&M AGRILIFE RESEARCH · PI CHAPKIN, ROBERT STEPHEN · 2016 to 2022
$6.3M
Diet and the colonic exfoliome: a novel, non-invasive approach to testing interventions in humansR21CA245456 · NCI · FRED HUTCHINSON CANCER RESEARCH CENTER · PI CHAPKIN, ROBERT STEPHEN, HULLAR, MEREDITH · 2020 to 2021
$446k
NCI NIH HHS R21 CA245456NCI NIH HHS R35 CA197707
6 · The paper itself

Abstract

Diet is an important risk factor for colorectal cancer (CRC), and several dietary constituents implicated in CRC are modified by gut microbial metabolism. Microbial fermentation of dietary fiber produces short-chain fatty acids, e.g., acetate, propionate, and butyrate. Dietary fiber has been shown to reduce colon tumors in animal models, and, in vitro, butyrate influences cellular pathways important to cancer risk. Furthermore, work from our group suggests that the combined effects of butyrate and omega-3 polyunsaturated fatty acids (n-3 PUFA) may enhance the chemopreventive potential of these dietary constituents. We postulate that the relatively low intakes of n-3 PUFA and fiber in Western populations and the failure to address interactions between these dietary components may explain why chemoprotective effects of n-3 PUFA and fermentable fibers have not been detected consistently in prospective cohort studies. In this review, we summarize the evidence outlining the effects of n-3 long-chain PUFA and highly fermentable fiber with respect to alterations in critical pathways important to CRC prevention, particularly intrinsic mitochondrial-mediated programmed cell death resulting from the accumulation of lipid reactive oxygen species (ferroptosis), and epigenetic programming related to lipid catabolism and beta-oxidation-associated genes.

Indexed as

AnimalsApoptosisColorectal NeoplasmsDietDietary FiberDiet TherapyFatty Acids, Omega-3Gastrointestinal MicrobiomeHumansDietary FiberFatty Acids, Omega-3Colon cancerDiet interactionFermentable fiberFerroptosisn-3 PUFA

Identifiers

PMID32006211
PMCPMC7605510
OpenAlexW3003455818

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.