Evidence map›Paper›PMID 26853468›Full record

ArticleOncogene2016

Inhibition of colon cancer growth by docosahexaenoic acid involves autocrine production of TNFα.

A Fluckiger, A Dumont, V Derangère, C Rébé, C de Rosny, S Causse, C Thomas, L Apetoh, A Hichami, F Ghiringhelli and 1 more

Open access · bronzeAbstract read
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In one paragraph

Article in Oncogene, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
2.9field-weighted citation impact, top 10% 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

27 citing papers in PubMed, 48 citations in OpenAlex.

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  8. Key promoters of tumor hallmarks.International journal of clinical oncology · 2022
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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

11 authors at 1 institution in 1 country.

A FluckigerInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
A DumontInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
V DerangèreInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
C RébéInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
C de RosnyInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
S CausseInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
C ThomasInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
L ApetohInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.ORCID 0000-0002-2774-438X
A HichamiInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
F GhiringhelliInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
M RiallandInstitut National de la Santé et de la Recherche Médicale (INSERM) UMR 866, Dijon, France.
Inserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The omega-3 polyunsaturated fatty acid docosahexaenoic acid (DHA) has anti-inflammatory and anti-cancer properties. Among pro-inflammatory mediators, tumor necrosis factor α (TNFα) plays a paradoxical role in cancer biology with induction of cancer cell death or survival depending on the cellular context. The objective of the study was to evaluate the role of TNFα in DHA-mediated tumor growth inhibition and colon cancer cell death. The treatment of human colorectal cancer cells, HCT-116 and HCT-8 cells, with DHA triggered apoptosis in autocrine TNFα-dependent manner. We demonstrated that DHA-induced increased content of TNFα mRNA occurred through a post-transcriptional regulation via the down-regulation of microRNA-21 (miR-21) expression. Treatment with DHA led to nuclear accumulation of Foxo3a that bounds to the miR-21 promoter triggering its transcriptional repression. Moreover, inhibition of RIP1 kinase and AMP-activated protein kinase α reduced Foxo3a nuclear-cytoplasmic shuttling and subsequent increase of TNFα expression through a decrease of miR-21 expression in DHA-treated colon cancer cells. Finally, we were able to show in HCT-116 xenograft tumor-bearing nude mice that a DHA-enriched diet induced a decrease of human miR-21 expression and an increase of human TNFα mRNA expression limiting tumor growth in a cancer cell-derived TNFα dependent manner. Altogether, the present work highlights a novel mechanism for anti-cancer action of DHA involving colon cancer cell death mediated through autocrine action of TNFα.

Indexed as

AnimalsApoptosisAutocrine CommunicationColonic NeoplasmsDocosahexaenoic AcidsForkhead Box Protein O3Gene Expression Regulation, NeoplasticHCT116 CellsHumansMiceMicroRNAsTumor Necrosis Factor-alphaXenograft Model Antitumor AssaysDocosahexaenoic AcidsForkhead Box Protein O3FOXO3 protein, humanMicroRNAsMIRN21 microRNA, humanTumor Necrosis Factor-alpha

Identifiers

PMID26853468
OpenAlexW2264397534

What OpenQuestion holds

Textmetadata
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.