Abstract LB155: Increase in Pseudomonas and Shigella is associated to disease severity and Veillonella parvula is linked to promoter DNA methylation levels in endoscopic gastric biopsies

Abstract Introduction: Clinically useful molecular tools to triage gastric cancer patients in low resource settings are not currently available. We previously found that promoter methylation of IRF4, ELMO1, CLIP4 and MSC and a Global DNA Methylation Index > 4 in endoscopic biopsies, can be used as a molecular tool in gastric cancer risk stratification algorithms. We hypothesized that the microbiota provides a broad spectrum of taxa identification, a distinct sequence read record, and robust detection sensitivity, which can be used in gastric cancer risk stratification algorithms. Methods: We performed 16sRNA metagenomic sequencing to study the association between the gastric epithelium microbiome and DNA methylation alterations previously associated to gastric cancer risk in endoscopic tissue samples from a subset of cancer (n=14) and gastritis (n=10) participants from a prospective, observational study (n= 576) in high-risk gastric cancer clinics in Lima, Peru. The inclusion criterion were gastro-duodenal symptoms (ICD9-CM code 535) for gastritis controls and a clinical diagnosis of gastric cancer (ICD9-CM code 151) for cases, all determined by pathologists in Peru. A pathologist at Johns Hopkins School of Medicine reviewed a random sample of slides. Informed written consent was obtained from all patients included in the study. The Institutional Review Board of Johns Hopkins School of Medicine (NA_00020633) approved the research protocols. Results: Beta diversity comparisons using non-metric multidimensional scaling (NMDS), discriminated cancer from gastritis samples. We identified a predominance of Helicobacter pylori (p=0.001), Pseudomonas(p=0.002) and Shigella (p=0.005) in cancer samples. We also found and inverse association between Veillonella parvula (p=0.03) and DNA methylation of IRF4, ELMO1, CLIP4 and MSC in cancer samples. Conclusion: Preliminary results warrant further exploration of DNA methylation and microbiome linkages in the transition from a normal to a premalignant gastric phenotype, which can be used to develop affordable PCR based, point-of-care assays, for high-risk gastric cancer clinics worldwide. Citation Format: Laura Palmieri, Kelvin Navarro, Robert Gilman, Martha Jahuira Arias, Anne Jedlicka, Amanda Dziedzic, Ashley Ramos-Lopez, Amanda Garcia Negron, Juan Combe, Gloria Vargas, William Prado, James White, Mariana Brait, David Sidransky, Filipa Godoy Vitorino, Rafael E. Guerrero-Preston. Increase in Pseudomonas and Shigella is associated to disease severity and Veillonella parvula is linked to promoter DNA methylation levels in endoscopic gastric biopsies [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_2):Abstract nr LB155.

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Journal
Cancer Research
Published
2025-04-25
DOI
https://doi.org/10.1158/1538-7445.am2025-lb155
Primary Topic
Enterobacteriaceae and Cronobacter Research
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article

Abstract LB155: Increase in Pseudomonas and Shigella is associated to disease severity and Veillonella parvula is linked to promoter DNA methylation levels in endoscopic gastric biopsies

Filipa Godoy‐Vitorino, Ashley Ramos-Lopez, Amanda Dziedzic, Laura Palmieri et al.
Cancer Research
Enterobacteriaceae and Cronobacter Research
article

Abstract LB155: Increase in Pseudomonas and Shigella is associated to disease severity and Veillonella parvula is linked to promoter DNA methylation levels in endoscopic gastric biopsies

Filipa Godoy‐Vitorino, Ashley Ramos-Lopez, Amanda Dziedzic, Laura Palmieri, Martha Jahuira Arias, James R. White, Amanda García Negrón, Rafael Guerrero‐Preston, Anne Jedlicka, Kelvin Navarro, Mariana Brait, Robert H. Gilman, David Sidransky, J Combe, Gloria Vargas, W.A. Prado
article en

Abstract

Abstract Introduction: Clinically useful molecular tools to triage gastric cancer patients in low resource settings are not currently available. We previously found that promoter methylation of IRF4, ELMO1, CLIP4 and MSC and a Global DNA Methylation Index > 4 in endoscopic biopsies, can be used as a molecular tool in gastric cancer risk stratification algorithms. We hypothesized that the microbiota provides a broad spectrum of taxa identification, a distinct sequence read record, and robust detection sensitivity, which can be used in gastric cancer risk stratification algorithms. Methods: We performed 16sRNA metagenomic sequencing to study the association between the gastric epithelium microbiome and DNA methylation alterations previously associated to gastric cancer risk in endoscopic tissue samples from a subset of cancer (n=14) and gastritis (n=10) participants from a prospective, observational study (n= 576) in high-risk gastric cancer clinics in Lima, Peru. The inclusion criterion were gastro-duodenal symptoms (ICD9-CM code 535) for gastritis controls and a clinical diagnosis of gastric cancer (ICD9-CM code 151) for cases, all determined by pathologists in Peru. A pathologist at Johns Hopkins School of Medicine reviewed a random sample of slides. Informed written consent was obtained from all patients included in the study. The Institutional Review Board of Johns Hopkins School of Medicine (NA_00020633) approved the research protocols. Results: Beta diversity comparisons using non-metric multidimensional scaling (NMDS), discriminated cancer from gastritis samples. We identified a predominance of Helicobacter pylori (p=0.001), Pseudomonas(p=0.002) and Shigella (p=0.005) in cancer samples. We also found and inverse association between Veillonella parvula (p=0.03) and DNA methylation of IRF4, ELMO1, CLIP4 and MSC in cancer samples. Conclusion: Preliminary results warrant further exploration of DNA methylation and microbiome linkages in the transition from a normal to a premalignant gastric phenotype, which can be used to develop affordable PCR based, point-of-care assays, for high-risk gastric cancer clinics worldwide. Citation Format: Laura Palmieri, Kelvin Navarro, Robert Gilman, Martha Jahuira Arias, Anne Jedlicka, Amanda Dziedzic, Ashley Ramos-Lopez, Amanda Garcia Negron, Juan Combe, Gloria Vargas, William Prado, James White, Mariana Brait, David Sidransky, Filipa Godoy Vitorino, Rafael E. Guerrero-Preston. Increase in Pseudomonas and Shigella is associated to disease severity and Veillonella parvula is linked to promoter DNA methylation levels in endoscopic gastric biopsies [abstract]. In: Proceedings of the American Association for Cancer Research Annual Meeting 2025; Part 2 (Late-Breaking, Clinical Trial, and Invited Abstracts); 2025 Apr 25-30; Chicago, IL. Philadelphia (PA): AACR; Cancer Res 2025;85(8_Suppl_2):Abstract nr LB155.

Cancer ResearchVol. 85(8_Supplement_2)
Johns Hopkins University (US), InterAmerican University of Puerto Rico (PR), Universidad Peruana Cayetano Heredia (PE), University of Puerto Rico System (PR), Hospital Israelita Albert Einstein (BR), Instituto Nacional de Enfermedades Neoplásicas (PE), Hospital Nacional Dos de Mayo (PE), Resphera Biosciences (US), University of Baltimore (US)
Openalex Percentile: Top 93%
Enterobacteriaceae and Cronobacter Research
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