Annual Meeting of the NCI Cohort Consortium (Abstract Submission): Submission #14
Submission information
Submission Number: 14
Submission ID: 154343
Submission UUID: 423423e7-449d-4e2b-b61c-84ebcae30132
Submission URI: /egrp/cohortconsortium/abstracts?cid=eb_govdel
Submission Update: /egrp/cohortconsortium/abstracts?cid=eb_govdel&token=YQyqmrLtSxTZeJ7TTiAsKNZ5DTMgnYQS-fH89n7feTM
Created: Wed, 09/10/2025 - 21:25
Completed: Wed, 09/10/2025 - 21:42
Changed: Wed, 09/10/2025 - 21:42
Remote IP address: 10.208.28.116
Submitted by: Anonymous
Language: English
Is draft: No
Webform: Cohort 2025 (Abstracts Submission)
Lightning Talks Abstract
Yixuan
Meng
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Ph.D
NYU Grossman School of Medicine
Oral Bacterial and Fungal Microbiome and Subsequent Risk for Pancreatic Cancer
Importance: The oral microbiota may be involved in the development of pancreatic cancer, yet current evidence is largely limited to bacterial 16S amplicon sequencing and small retrospective case‒control studies.
Objective: To test whether the oral bacterial and fungal microbiome is associated with the subsequent development of pancreatic cancer.
Design: This cohort study used data from 2 epidemiological cohorts: the American Cancer Society Cancer Prevention Study-II Nutrition Cohort and the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
Exposures: The oral bacterial and fungal microbiome were characterized via whole-genome shotgun sequencing and internal transcribed spacer (ITS) sequencing, respectively. The association of the microbiome-wide bacterial and fungal taxa with pancreatic cancer was assessed by Analysis of Compositions of Microbiomes with Bias Correction 2 (ANCOM-BC2).
Results: Three oral bacterial periodontal pathogens—Porphyromonas gingivalis, Eubacterium nodatum, and Parvimonas micra—were associated with increased risk for pancreatic cancer. A bacteriome-wide scan revealed 8 oral bacteria associated with decreased and 13 oral bacteria associated with increased risk of pancreatic cancer (false discovery rate-adjusted q-values<0.05). Of the fungi, genus Candida was associated with increased risk of pancreatic cancer. The microbial risk score (MRS), based on 27 oral species, was associated with an increase in pancreatic cancer risk (multivariate odds ratio per 1-SD increase in MRS, 3.44, 95% CI, 2.63–4.51).
Conclusions: In this cohort study, oral bacteria and fungi were significant risk factors for pancreatic cancer development. Oral microbiota hold promises as biomarkers to identify individuals at high risk of pancreatic cancer, potentially contributing to personalized prevention.
Objective: To test whether the oral bacterial and fungal microbiome is associated with the subsequent development of pancreatic cancer.
Design: This cohort study used data from 2 epidemiological cohorts: the American Cancer Society Cancer Prevention Study-II Nutrition Cohort and the Prostate, Lung, Colorectal, and Ovarian Cancer Screening Trial.
Exposures: The oral bacterial and fungal microbiome were characterized via whole-genome shotgun sequencing and internal transcribed spacer (ITS) sequencing, respectively. The association of the microbiome-wide bacterial and fungal taxa with pancreatic cancer was assessed by Analysis of Compositions of Microbiomes with Bias Correction 2 (ANCOM-BC2).
Results: Three oral bacterial periodontal pathogens—Porphyromonas gingivalis, Eubacterium nodatum, and Parvimonas micra—were associated with increased risk for pancreatic cancer. A bacteriome-wide scan revealed 8 oral bacteria associated with decreased and 13 oral bacteria associated with increased risk of pancreatic cancer (false discovery rate-adjusted q-values<0.05). Of the fungi, genus Candida was associated with increased risk of pancreatic cancer. The microbial risk score (MRS), based on 27 oral species, was associated with an increase in pancreatic cancer risk (multivariate odds ratio per 1-SD increase in MRS, 3.44, 95% CI, 2.63–4.51).
Conclusions: In this cohort study, oral bacteria and fungi were significant risk factors for pancreatic cancer development. Oral microbiota hold promises as biomarkers to identify individuals at high risk of pancreatic cancer, potentially contributing to personalized prevention.