Oral and fecal microbiome alterations in pancreatic cancer: insights into potential diagnostic biomarkers

From BugSigDB
Needs review
study design
Citation
PMID PubMed identifier for scientific articles.
DOI Digital object identifier for electronic documents.
URI Uniform resource identifier for web resources.
Authors
Tavanaeian S., Feizabadi M.M., Falsafi S., Aghdaei H.A., Houri H.
Journal
BMC microbiology
Year
2025
Keywords:
Fusobacterium nucleatum, Neisseria elongata, Fecal microbiome, Oral microbiome, Pancreatic cancer
BACKGROUND: The human microbiome plays a pivotal role in pancreatic cancer (PC). This study investigates the abundance of specific gut and oral microbes in PC patients compared to healthy controls. METHODS: A cohort of 20 diagnosed PC patients and an equivalent control group were recruited. Comprehensive lifestyle data, such as overall food consumption, were collected. Saliva and stool samples were prepared. Microbial DNA was extracted from stool and saliva samples using specialized kits. Primers were designed targeting the conserved regions of the 16 S rRNA genes from Neisseria elongata, Granulicatella adiacens, Fusobacterium nucleatum, Roseburia intestinalis, and Bifidobacterium bifidum. The quantities of selected bacterial species were evaluated using real-time quantitative PCR. RESULTS: Granulicatella adiacens and Fusobacterium nucleatum were significantly increased in the PC group (medians: 7.35 and 4.37 log10 CFU/g, respectively) compared to controls (medians: 2.43 and 1.20 log10 CFU/g ; P < 0.001 for both). Conversely, Neisseria elongata, Roseburia intestinalis, and Bifidobacterium bifidum levels were significantly lower in PC patients (medians: 2.37, 2.34, and 3.45 log10 CFU/g, respectively) compared to controls (medians: 5.63, 5.07, and 4.34 log10 CFU/g; P < 0.001). The principal component analysis confirmed distinct clustering of microbiota profiles between the two groups, with key microorganisms associated with PC. The discriminatory performance of clinical and microbiota variables demonstrated notable accuracy in classifying PC, particularly metrics such as hemoglobin and hematocrit, achieving an area under the curve (AUC) of 1.00. CONCLUSIONS: In summary, these findings highlight the significant association between microbiome composition and PC, underscoring the potential of microbiota profiles as non-invasive diagnostic biomarkers that warrant further investigation for early detection and therapeutic targeting in clinical practice. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12866-025-04344-2.

Experiment 1


Needs review

Curated date: 2025/10/13

Curator: Deborah-Fabusuyi

Revision editor(s): Deborah-Fabusuyi

Subjects

Location of subjects
Iran
Host species Species from which microbiome was sampled. Contact us to have more species added.
Homo sapiens
Body site Anatomical site where microbial samples were extracted from according to the Uber Anatomy Ontology
Feces Cow dung,Cow pat,Droppings,Dung,Excrement,Excreta,Faeces,Fecal material,Fecal matter,Fewmet,Frass,Guano,Matières fécales@fr,Merde@fr,Ordure,Partie de la merde@fr,Piece of shit,Porción de mierda@es,Portion of dung,Portion of excrement,Portion of faeces,Portion of fecal material,Portion of fecal matter,Portion of feces,Portion of guano,Portion of scat,Portionem cacas,Scat,Spoor,Spraint,Stool,Teil der fäkalien@de,Feces,feces
Condition The experimental condition / phenotype studied according to the Experimental Factor Ontology
Pancreatic carcinoma cancer of pancreas,cancer of the pancreas,carcinoma of exocrine pancreas,carcinoma of pancreas,carcinoma of the pancreas,exocrine cancer,exocrine pancreas carcinoma,exocrine pancreatic carcinoma,pancreas cancer,pancreas carcinoma,pancreatic cancer,pancreatic cancer (not islets),pancreatic carcinoma,pancreatic carcinoma, familial,Pancreatic carcinoma
Group 0 name Corresponds to the control (unexposed) group for case-control studies
Healthy control group
Group 1 name Corresponds to the case (exposed) group for case-control studies
Pancreatic cancer patients
Group 1 definition Diagnostic criteria applied to define the specific condition / phenotype represented in the case (exposed) group
Newly diagnosed Pancreatic cancer patients between the ages of 20 -70 who have not begun treatments
Group 0 sample size Number of subjects in the control (unexposed) group
20
Group 1 sample size Number of subjects in the case (exposed) group
20

Lab analysis

Sequencing type
16S
16S variable region One or more hypervariable region(s) of the bacterial 16S gene
Not specified
Sequencing platform Manufacturer and experimental platform used for quantifying microbial abundance
RT-qPCR

Statistical Analysis

Data transformation Data transformation applied to microbial abundance measurements prior to differential abundance testing (if any).
relative abundances
Statistical test
Mann-Whitney (Wilcoxon)
Significance threshold p-value or FDR threshold used for differential abundance testing (if any)
0.05
MHT correction Have statistical tests be corrected for multiple hypothesis testing (MHT)?
No


Signature 1

Needs review

Curated date: 2025/10/13

Curator: Deborah-Fabusuyi

Revision editor(s): Deborah-Fabusuyi

Source: Fig. 1

Description: Differential abundance of gut microbiota between Pancreatic Cancer patients and healthy controls.

Abundance in Group 1: increased abundance in Pancreatic cancer patients

NCBI Quality ControlLinks
Fusobacterium nucleatum

Revision editor(s): Deborah-Fabusuyi

Signature 2

Needs review

Curated date: 2025/10/13

Curator: Deborah-Fabusuyi

Revision editor(s): Deborah-Fabusuyi

Source: Fig. 1

Description: Differential abundance of gut microbiota between Pancreatic Cancer patients and healthy controls.

Abundance in Group 1: decreased abundance in Pancreatic cancer patients

NCBI Quality ControlLinks
Bifidobacterium bifidum
Roseburia intestinalis

Revision editor(s): Deborah-Fabusuyi

Experiment 2


Needs review

Curated date: 2025/10/13

Curator: Deborah-Fabusuyi

Revision editor(s): Deborah-Fabusuyi

Differences from previous experiment shown

Subjects

Body site Anatomical site where microbial samples were extracted from according to the Uber Anatomy Ontology
Saliva Sailva normalis,Saliva atomaris,Saliva molecularis,Salivary gland secretion,Saliva,saliva


Lab analysis

Statistical Analysis

Signature 1

Needs review

Curated date: 2025/10/13

Curator: Deborah-Fabusuyi

Revision editor(s): Deborah-Fabusuyi

Source: Fig. 1

Description: Differential abundance of oral microbiota between Pancreatic Cancer patients and healthy controls.

Abundance in Group 1: increased abundance in Pancreatic cancer patients

NCBI Quality ControlLinks
Granulicatella adiacens

Revision editor(s): Deborah-Fabusuyi

Signature 2

Needs review

Curated date: 2025/10/13

Curator: Deborah-Fabusuyi

Revision editor(s): Deborah-Fabusuyi

Source: Fig. 1

Description: Differential abundance of oral microbiota between Pancreatic Cancer patients and healthy controls.

Abundance in Group 1: decreased abundance in Pancreatic cancer patients

NCBI Quality ControlLinks
Neisseria elongata

Revision editor(s): Deborah-Fabusuyi