ArticleMolecular biology reports2025
Assessing the role of Escherichia coli and Klebsiella pneumoniae in colorectal cancer oncogene expression: insights from microbial colonization phenotypes.
Article in Molecular biology reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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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.
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.
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Who cites it
4 citing papers in PubMed.
- Evolutionary Genomics of Human Gut Bacteria: Ecological Plasticity Across the Mutualism-Pathogenicity Spectrum.International journal of molecular sciences · 2026Review
- Establishing the role of the neurotransmitter receptor-related geneTranslational cancer research · 2026Article
- Review
- Secretion of Extracellular Microvesicles Induced by a Fraction ofInternational journal of molecular sciences · 2025Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
7 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundColorectal cancer (CRC) remains a major global health burden, ranking as the third most prevalent malignancy and the second leading cause of cancer-related mortality. Its pathogenesis involves complex interactions between genetic, environmental, and lifestyle factors, with emerging evidence implicating the gut microbiome as a key contributor. Specific pathobionts, such as Escherichia coli and Klebsiella pneumoniae, have been linked to CRC progression due to their pro-inflammatory properties. This study investigated the association of E. coli and K. pneumoniae with CRC tissues and their influence on oncogenic gene expression, particularly within the TGF-β, Notch, Wnt/β-catenin, Rho GTPase, and EGFR/MAPK signaling pathways.
methodsUsing both culture and molecular-based methods, we analyzed 100 CRC patient biopsies from Taleghani Hospital, Tehran (July 2021-May 2023), assessing bacterial presence and the expression of 19 CRC-associated genes. Adhesion and invasion capabilities of isolates were evaluated in Caco-2 cells.
resultsWhile clinical parameters (e.g., age, survival, tumor stage) did not differ significantly between bacterial groups, gene expression analysis revealed elevated FOLH1 and MAP2K1 in adhesive-invasive K. pneumoniae isolates and increased FOLH1 in E. coli-positive samples. Tumor stage- and site-specific variations were observed, such as heightened ANXA3 expression in Stage I tumors harboring K. pneumoniae. Principal component analysis (PCA) demonstrated overlapping oncogenic profiles, suggesting complex, context-dependent microbial influences.
conclusionsOur findings indicate that E. coli and K. pneumoniae may exert nuanced, tumor-specific effects on oncogenic pathways, potentially mediated more by chronic inflammation than direct gene dysregulation. Further studies employing single-cell RNA sequencing are warranted to elucidate these interactions and their translational potential for CRC diagnostics and therapeutics.
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Registered trials
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