Evidence map›Paper›PMID 41452506›Full record

ArticleMedical oncology (Northwood, London, England)2025

Microbiota relationship between breast, colorectal, and lung cancer types.

Ebru Kanimdan, Caspar Bundgaard-Nielsen, Vildan Betul Yenigun, Burcu Gul, Zuhal Gucin, Hasan Enis Komurcu, Sahende Elagoz, Ozge Pasin, Suzette Sørensen, Ercan Arican

Abstract read
PubMed Publisher
In one paragraph

Article in Medical oncology (Northwood, London, England), 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. 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

10 authors.

Ebru KanimdanInstitute of Graduate Studies in Science, Molecular Biology and Genetics Department, Istanbul University, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-7123-4600
Caspar Bundgaard-NielsenCentre for Clinical Research, North Denmark Regional Hospital, Aalborg, Denmark.ORCID http://orcid.org/0000-0002-2700-2378
Vildan Betul YenigunVocational School of Health Services, Bezmialem Vakif University, Istanbul, Turkey.ORCID http://orcid.org/0000-0002-8021-8629
Burcu GulFaculty of Medicine, Department of Medical Pathology, Bezmialem Vakif University, Istanbul, Turkey.ORCID http://orcid.org/0000-0003-3705-2464
Zuhal GucinFaculty of Medicine, Department of Medical Pathology, Bezmialem Vakif University, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-5330-2158
Hasan Enis KomurcuFaculty of Medicine, Department of Medical Pathology, Bezmialem Vakif University, Istanbul, Turkey.
Sahende ElagozFaculty of Medicine, Department of Medical Pathology, Bezmialem Vakif University, Istanbul, Turkey.
Ozge PasinDepartment of Biostatistics, Hamidiye Medical Faculty, Health Sciences University, Istanbul, Turkey.ORCID http://orcid.org/0000-0001-6530-0942
Suzette SørensenCentre for Clinical Research, North Denmark Regional Hospital, Aalborg, Denmark.ORCID http://orcid.org/0000-0002-4201-1168
Ercan AricanScience Faculty, Molecular Biology and Genetics Department, Istanbul University, Istanbul, Turkey. earican@istanbul.edu.tr.ORCID http://orcid.org/0000-0002-1676-5919

Funding

Bilimsel Araştirma Projeleri Birimi, Istanbul Üniversitesi 39019
6 · The paper itself

Abstract

Colorectal cancer (CRC), breast cancer (BC), and lung cancer (LC) are among the most common and deadly malignancies worldwide. In recent years, the role of tumor-associated microbiota in the initiation and progression of cancer has attracted increasing attention. However, studies examining different cancer types together with their clinical stages remain limited. The aim of this study was to compare the composition of tumor tissue microbiota across three cancer types and different disease stages. For this purpose, DNA was isolated from formalin-fixed paraffin-embedded (FFPE) tumor samples, and sequencing of the 16 S rRNA gene region was performed. Microbial profiles were analyzed at the phylum and genus levels, and diversity indices were compared between groups. In stage III LC samples, the phylum Cyanobacteria was found to be markedly more abundant compared to other stages. In CRC, the phylum Firmicutes was most abundant in stage III tumors, showing higher levels than in early stages. In metastatic cases (advanced stages), both the operational taxonomic unit (OTU) count and Shannon diversity index were found to be highly similar to those of LC control tissues but markedly lower than those of the CRC control group. Across all cancer types, Actinobacteria, Cyanobacteria, Proteobacteria, and Firmicutes were identified as the dominant phyla, though their relative abundances varied by cancer type and stage. The findings suggest that tumor-associated microbiota composition exhibits distinct signatures depending on tumor type and progression stage. Similarities observed between certain cancer types and stages may indicate the presence of shared microbial patterns within the tumor microenvironment. Such microbial signatures may serve as potential biomarkers for diagnosis, prognosis, or therapeutic targeting.

Indexed as

Breast NeoplasmsColorectal NeoplasmsLung NeoplasmsMicrobiotaAgedFemaleHumansMaleMiddle AgedRNA, Ribosomal, 16SRNA, Ribosomal, 16SBreast cancerColorectal cancerFFPEFull-length 16S rRNA geneLung cancerMicrobiota

Identifiers

What OpenQuestion holds

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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.