Evidence map›Paper›PMID 41333806›Full record

ArticleFrontiers in cellular and infection microbiology2025

Metagenomic analysis of gut microbiota in colorectal adenocarcinoma in the MENA region.

Mohammad T Al Bataineh, Nihar Ranjan Dash, Mohamed Mysara, Omnia Saeed, Noura Alkhayyal, Iman M Talaat, Riyad Bendardaf, Maha Saber-Ayad

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–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

1 citing paper in PubMed.

  1. IntratumoralAnimals : an open access journal from MDPI · 2026
    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

8 authors.

Mohammad T Al BatainehDepartment of Basic Medical Sciences, College of Medicine, Yarmouk University, Irbid, Jordan.
Nihar Ranjan DashClinical Sciences Department, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Mohamed MysaraBioinformatics Group, Center for Informatics Sciences (CIS), School of Information Technology and Computer Science (ITCS), Nile University, Giza, Egypt.
Omnia SaeedBioinformatics Group, Center for Informatics Sciences (CIS), School of Information Technology and Computer Science (ITCS), Nile University, Giza, Egypt.
Noura AlkhayyalOncology Department, University Hospital Sharjah, Sharjah, United Arab Emirates.
Iman M TalaatClinical Sciences Department, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.
Riyad BendardafResearch Institute for Medical and Health Sciences, University of Sharjah, Sharjah, United Arab Emirates.
Maha Saber-AyadClinical Sciences Department, College of Medicine, University of Sharjah, Sharjah, United Arab Emirates.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Growing evidence suggests that gut microbiota plays a role in the development of colorectal cancer (CRC), and a few bacterial strains have been linked to carcinogenesis. Contrary to the Western population, the relationship between pro-cancer microorganisms and CRC among Middle Eastern individuals remains largely unexplored. Ninety-eight samples from Middle Eastern individuals with and without CRC were subjected to microbial profiling based on the 16S rRNA gene. Results: The CRC group exhibited a more complex gut microbiota with clusters that were significantly distinct from those of the control group. The taxonomic orders Caulobacterales, Rhizobiales, Sphingomonadales, and Burkholderiales, along with the genera Recibecterium and Sphingobium, were overrepresented in the CRC samples based on differential abundance testing between the CRC and control groups. Utilizing 16S-based functional prediction, we identified a significant enrichment of pathways vital for pentose and glucuronate interconversions, metabolism of terpenoids and polyketides, spliceosome, and dTMP kinase pathways within the CRC group. Moreover, we observed a link between Herbaspirillum huttiense and the pathways regulating the actin cytoskeleton; this intriguing connection may provide insights into the molecular mechanisms underlying cytoskeletal rearrangement and carcinogenesis triggered by H. huttiense. Conclusions: The findings of this study support the connection between gut microbiota and the development of CRC and highlight region-specific microbial signatures that may serve as non-invasive diagnostic biomarkers or predictive tools for early screening in Middle Eastern populations, where CRC is increasingly diagnosed at advanced stages. These insights could inform the development of microbiome-based screening panels and personalized prevention strategies adapted to the MENA region's unique genetic, dietary, and environmental profiles.

Indexed as

AdenocarcinomaBacteriaColorectal NeoplasmsGastrointestinal MicrobiomeMetagenomicsAgedDNA, BacterialDNA, RibosomalFecesFemaleHumansMaleMiddle AgedMiddle EastPhylogenyRNA, Ribosomal, 16SDNA, BacterialDNA, RibosomalRNA, Ribosomal, 16Sadenocarcinomacolorectal cancerdysbiosismetagenomicsmicrobiota

Identifiers

PMID41333806
PMCPMC12665689

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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.