Evidence map›Paper›PMID 37206892›Full record

ArticleJournal of carcinogenesis & mutagenesis2022

Relationships between gut microbiota, red meat consumption and colorectal cancer.

Mahamane Talphi Diakité, Bréhima Diakité, Amadou Koné, Saidou Balam, Djeneba Fofana, Dramane Diallo, Yaya Kassogué, Cheick B Traoré, Bakarou Kamaté, Djibril Ba and 9 more

Abstract read
In one paragraph

Article in Journal of carcinogenesis & mutagenesis, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

26 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  4. Iron, inflammation, and intestinal tumors: the crucial triad in colorectal cancer progression and therapy.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
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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

19 authors.

Mahamane Talphi DiakitéUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Bréhima DiakitéUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Amadou KonéUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Saidou BalamUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Djeneba FofanaUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Dramane DialloUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Yaya KassoguéUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Cheick B TraoréUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Bakarou KamatéUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Djibril BaDepartment of Medicine, Pennsylvania State University College of Medicine, Hershey, Pennsylvania, United States.
Madani LyUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Mamadou BaUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Bourahima KonéUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Almoustapha I MaigaUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.
Chad AchenbachDepartment of Oncology, North-Western University, Chicago, Illinois, United States.
Jane HollDepartment of Neurology, University of Chicago, Chicago, Illinois, United States.
Robert MurphyDepartment of Oncology, North-Western University, Chicago, Illinois, United States.
Lifang HouDepartment of Oncology, North-Western University, Chicago, Illinois, United States.
Mamoudou MaigaUniversity of Sciences, Techniques and Technologies of Bamako (USTTB), Bamako, Mali.

Funding

Partnership for Global Health Research Training Program (Renewal)-Supplement for OBSSR, NCI, NCI-AIDS and NIDCDD43TW010543 · FIC · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI Wafaie W Fawzi, DAVIDSON HOWES HAMER · 2017 to 2026
$12.1M
HIV and Mycobacterial Disease in MaliD43TW010350 · FIC · UNIV OF SCIENCES, TECH & TECH OF BAMAKO · PI MAIGA, ALMOUSTAPHA ISSIAKA, MURPHY, ROBERT LEO · 2016 to 2025
$3.0M
Infection-Associated Cancer Research Training Program in MaliD43CA260658 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI HOU, LIFANG, MAIGA, MAMOUDOU · 2021 to 2025
$1.3M
Metabolic and Immune Consequences of Antibiotic-Related Microbiome Alterations during TB TreatmentR21AI148033 · NIAID · NORTHWESTERN UNIVERSITY · PI MAIGA, MAMOUDOU · 2019 to 2020
$440k
FIC NIH HHS D43 TW010350FIC NIH HHS D43 TW010543NCI NIH HHS D43 CA260658NIAID NIH HHS R21 AI148033
6 · The paper itself

Abstract

Excessive consumption of red and processed meat has been associated with a higher risk of developing colorectal cancer. There are many attempts to explain the risk of colorectal cancer associated with the consumption of red and processed meat: The temperature cooking of meat such as grilling and smoking contribute to the formation of mutagenic compounds including heterocyclic amines and polycyclic aromatic hydrocarbons.Heme iron in red meat is involved in the formation of N-nitroso compounds and lipid peroxidation products in the digestive tract.Fatty red meat is involved in the production of secondary bile acids by the bacteria of the gut microbiota. Many of the products formed are genotoxic and can cause DNA damage and initiate carcinogenesis of colorectal cancer. Various mechanisms contributing to their genotoxic role have been established in human and animal studies. In addition, there is increasing evidence that compounds formed from red and processed meat interact with the gut microbiota in colorectal cancer pathways. Although several early studies in animals and humans suggest a direct causal role of the gut microbiota in the development of colorectal cancer, the links between diet, gut microbiota, and colonic carcinogenesis are largely associations rather than proven causal relationships. Various biological mechanisms, including inflammation and oxidative stress can lead to DNA damage, gut dysbiosis, and therefore increase the risk of colorectal cancer. Dysbiosis of the gut microbiota may increase the risk of colorectal cancer through dietary component promotion of colonic carcinogenesis. In this paper, we review and update current knowledge about the relationships between red meat consumption, gut microbiota, and colorectal cancer.

Indexed as

Colorectal CancerDietDysbiosisGut microbiotaRed meat

Identifiers

PMID37206892
PMCPMC10194058

What OpenQuestion holds

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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.