Microbiome alterations in mismatch-repair deficient metastatic colorectal cancer patients

Abstract Colorectal cancer (CRC) is the second leading cause of cancer-related death worldwide. Many efforts have been made to stratify CRC cases, from investigating the genomic characteristics of the tumor to – more recently – considering the gut microbiome. Differences in the composition of the gut microbiome occur along CRC stages and according to primary tumor location. The microbiome links with other tumor characteristics remain underinvestigated, including those related to microsatellite instability, that have been so far assessed only with respect to intratumoral bacterial presence and not to the whole gut or oral microbiome. Here we study associations between tumor microsatellite instability and the microbiome by collecting oral and gut microbiome samples from two clinical trials, ARETHUSA and AtezoTRIBE, enrolling metastatic CRC (mCRC) patients with microsatellite stable (MSS) tumors and with high microsatellite instability (MSI-H) tumors. We identified a significant reduction in microbial diversity in oral and gut microbiomes of CRC patients with MSI-H compared to patients with MSS (Wilcoxon rank-sum test P = 0.001 and 0.005, respectively). In addition, the MSI-H condition could be predicted by machine learning algorithms (AUC of 0.7 for both stool and oral microbiome) and the microbial signature for this condition comprises fewer microbial species compared to MSS with Ligilactobacillus salivarius and Rothia mucilaginosa detected as the strongest MSI-H associated intestinal and oral species, respectively. Our work provides evidence of human microbiome connections with tumor genetic stability, and poses the basis for larger validating investigations and mechanistic studies.

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Publication Details

Journal
Scientific Reports
Published
2026-09-01
DOI
https://doi.org/10.1038/s41598-026-69169-z
Primary Topic
Gut microbiota and health
Type
article
Field-Weighted Citation Impact
0.00

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article

Microbiome alterations in mismatch-repair deficient metastatic colorectal cancer patients

Gianmarco Piccinno, Alessandra Raimondi, Francesco Asnicar, Michela Lizier et al.
Scientific Reports
Gut microbiota and health
article

Microbiome alterations in mismatch-repair deficient metastatic colorectal cancer patients

Gianmarco Piccinno, Alessandra Raimondi, Francesco Asnicar, Michela Lizier, Salvatore Siena, Lisa Derosa, Nicola Segata, Laurence Zitvogel, Filippo Pietrantonio, Silvia Marsoni, Carmen Correale, Federica Armanini, Katarina Mladenović, Michele Palazzo, Andrea Sartore-Bianchi, Federica Marmorino, Paolo Manghi, Luca Lazzari, Alberto Bardelli, Maria Rescigno, Chiara Cremolini, Chiara Pozzi
article en

Abstract

Abstract Colorectal cancer (CRC) is the second leading cause of cancer-related death worldwide. Many efforts have been made to stratify CRC cases, from investigating the genomic characteristics of the tumor to – more recently – considering the gut microbiome. Differences in the composition of the gut microbiome occur along CRC stages and according to primary tumor location. The microbiome links with other tumor characteristics remain underinvestigated, including those related to microsatellite instability, that have been so far assessed only with respect to intratumoral bacterial presence and not to the whole gut or oral microbiome. Here we study associations between tumor microsatellite instability and the microbiome by collecting oral and gut microbiome samples from two clinical trials, ARETHUSA and AtezoTRIBE, enrolling metastatic CRC (mCRC) patients with microsatellite stable (MSS) tumors and with high microsatellite instability (MSI-H) tumors. We identified a significant reduction in microbial diversity in oral and gut microbiomes of CRC patients with MSI-H compared to patients with MSS (Wilcoxon rank-sum test P = 0.001 and 0.005, respectively). In addition, the MSI-H condition could be predicted by machine learning algorithms (AUC of 0.7 for both stool and oral microbiome) and the microbial signature for this condition comprises fewer microbial species compared to MSS with Ligilactobacillus salivarius and Rothia mucilaginosa detected as the strongest MSI-H associated intestinal and oral species, respectively. Our work provides evidence of human microbiome connections with tumor genetic stability, and poses the basis for larger validating investigations and mechanistic studies.

Scientific Reports
University of Pisa (IT), Humanitas University (IT), Inserm (FR), University of Milan (IT), University of Trento (IT), Université Paris-Saclay (FR), Institut Gustave Roussy (FR), Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda (IT), La Ligue Contre le Cancer (FR), IFOM (IT), Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancers (FR), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Fondazione IRCCS Istituto Nazionale dei Tumori (IT), IRCCS Humanitas Research Hospital (IT), University of Turin (IT), European Institute of Oncology (IT)
Cancer Research UK, European Commission, Ministero dell’Istruzione, dell’Università e della Ricerca, Associazione Italiana per la Ricerca sul Cancro, National Institutes of Health, Horizon 2020 Framework Programme, MSD Italia, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 18%
Gut microbiota and health
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Microbiome alterations in mismatch-repair deficient metastatic colorectal cancer patients — Gianmarco Piccinno, Alessandra Raimondi, et al. · Scientific Reports (2026) | TGRS Research Map | TGRS