Evidence map›Paper›PMID 35159382›Full record

ArticleCells2022

Metabolomics of Acute vs. Chronic Spinach Intake in an Apc-Mutant Genetic Background: Linoleate and Butanoate Metabolites Targeting HDAC Activity and IFN-γ Signaling.

Ying-Shiuan Chen, Jia Li, Sultan Neja, Sabeeta Kapoor, Jorge Enrique Tovar Perez, Chakrapani Tripathi, Rani Menon, Arul Jayaraman, Kyongbum Lee, Wan Mohaiza Dashwood and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
0.4field-weighted citation impact, top 43% 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

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
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

15 authors at 5 institutions in 2 countries.

Ying-Shiuan ChenCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Jia LiCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Sultan NejaCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.ORCID 0000-0003-3972-0016
Sabeeta KapoorCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Jorge Enrique Tovar PerezCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Chakrapani TripathiCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Rani MenonDepartment of Chemical Engineering, College of Engineering, Texas A&M University, College Station, TX 77840, USA.
Arul JayaramanDepartment of Chemical Engineering, College of Engineering, Texas A&M University, College Station, TX 77840, USA.
Kyongbum LeeDepartment of Chemical and Biological Engineering, Tufts University, Medford, MA 02155, USA.ORCID 0000-0002-0699-8057
Wan Mohaiza DashwoodCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Shan WangDepartment of Biology and Biochemistry, University of Houston, Houston, TX 77204, USA.
Ke ZhangCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Koichi KobayashiDepartment of Immunology, Hokkaido University Graduate School of Medicine, Sapporo 060-8638, Japan.ORCID 0000-0003-2930-0114
Praveen RajendranCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.
Roderick DashwoodCenter for Epigenetics & Disease Prevention, Texas A&M Health, Houston, TX 77030, USA.ORCID 0000-0003-0351-4034
Texas A&M University · USThe University of Texas MD Anderson Cancer Center · USTexas A&M Health Science Center · USTufts University · USUniversity of Houston · US

Funding

Dietary HDAC Inhibitors in Colon Cancer PreventionR01CA122959 · NCI · TEXAS A&M UNIVERSITY HEALTH SCIENCE CTR · PI DASHWOOD, RODERICK H · 2008 to 2023
$4.3M
NCI NIH HHS R01 CA122959
6 · The paper itself

Abstract

There is growing interest in the crosstalk between the gut microbiome, host metabolomic features, and disease pathogenesis. The current investigation compared long-term (26 week) and acute (3 day) dietary spinach intake in a genetic model of colorectal cancer. Metabolomic analyses in the polyposis in rat colon (Pirc) model and in wild-type animals corroborated key contributions to anticancer outcomes by spinach-derived linoleate bioactives and a butanoate metabolite linked to increased α-diversity of the gut microbiome. Combining linoleate and butanoate metabolites in human colon cancer cells revealed enhanced apoptosis and reduced cell viability, paralleling the apoptosis induction in colon tumors from rats given long-term spinach treatment. Mechanistic studies in cell-based assays and in vivo implicated the linoleate and butanoate metabolites in targeting histone deacetylase (HDAC) activity and the interferon-γ (IFN-γ) signaling axis. Clinical translation of these findings to at-risk patients might provide valuable quality-of-life benefits by delaying surgical interventions and drug therapies with adverse side effects.

Indexed as

Butyric AcidColonic NeoplasmsDietLinoleic AcidSpinacia oleraceaAnimalsHumansInterferon-gammaMetabolomicsRatsButyric AcidInterferon-gammaLinoleic AcidFamilial Adenomatous Polyposisgut microbiomehistone deacetylaseinterferon–γ signalingmajor histocompatibility complexpolyposis in rat colonspinach

Identifiers

PMID35159382
PMCPMC8834217
OpenAlexW4210920145

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.