Evidence map›Paper›PMID 42291310›Full record

ArticleFrontiers in cellular and infection microbiology2026

PCR profiling of tumor-associated microorganisms in tissue of primary epithelial malignant tumors of colorectal origin: associations with key clinicopathological characteristics.

Nikolay K Shakhpazyan, Liudmila M Mikhaleva, Nikolay K Sadykhov, Konstantin Y Midiber, Roman V Afanasev, Zarina V Gioeva, Alexander I Mikhalev, Arkady L Bedzhanyan

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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.

2 · The registry

The trial behind it

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

8 authors.

Nikolay K ShakhpazyanAvtsyn Research Institute of Human Morphology, Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.
Liudmila M MikhalevaAvtsyn Research Institute of Human Morphology, Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.
Nikolay K SadykhovAvtsyn Research Institute of Human Morphology, Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.
Konstantin Y MidiberAvtsyn Research Institute of Human Morphology, Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.
Roman V AfanasevAvtsyn Research Institute of Human Morphology, Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.
Zarina V GioevaAvtsyn Research Institute of Human Morphology, Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.
Alexander I MikhalevDepartment of Hospital Surgery No. 2, Pirogov Russian National Research Medical University, Moscow, Russia.
Arkady L BedzhanyanDepartment of Abdominal Surgery and Oncology II (Coloproctology and Uro-Gynecology), Russian National Research Center of Surgery named after B.V. Petrovsky, Moscow, Russia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Colorectal cancer is one of the most common malignancies worldwide, and microbiome research has strong potential to advance understanding of tumor biology and to support biomarker development and microbiome-targeted interventions. Most colorectal cancer microbiome studies rely on stool or mucosal sampling, but routine pathology archives contain abundant formalin-fixed, paraffin-embedded primary tumor tissue that could enable scalable assessment of tumor-associated microorganisms. Methods: We profiled tumor-associated microorganisms in primary colorectal adenocarcinoma specimens from 192 patients using a targeted quantitative PCR panel and evaluated associations with clinicopathological variables (tumor differentiation grade, primary tumor T category, and disease stage) using non-parametric tests, ordinal regression, regularized logistic regression, and within-panel profile ordination with permutation-based inference. Results: The most consistent signals were linked to tumor differentiation rather than stage. Tumors in the G2-G3 versus G1 comparison showed higher total bacterial load and a higher detection frequency of Conclusions: Targeted quantitative PCR profiling of archived primary tumor tissue identifies reproducible microbiome signals that track tumor differentiation grade more strongly than stage, suggesting that tissue bacterial burden and selected taxa may reflect microenvironmental features associated with the G2-G3 versus G1 contrast. Broader tumor microbiome profiling should be required to capture diversity and refine clinically informative signatures.

Indexed as

AdenocarcinomaBacteriaColorectal NeoplasmsMicrobiotaAgedAged, 80 and overBacterial LoadFemaleHumansMaleMiddle AgedReal-Time Polymerase Chain Reactionbacterial loadcolorectal neoplasmsneoplasm gradingreal-time polymerase chain reactionRuminococcus

Identifiers

PMID42291310
PMCPMC13253444

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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.