<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>22(1)</volume><submitter>Lowenmark T</submitter><funding>Umea University</funding><pubmed_abstract>&lt;h4>Background&lt;/h4>Mounting evidence suggests a significant role of the gut microbiota in the development and progression of colorectal cancer (CRC). In particular, an over-representation of oral pathogens has been linked to CRC. The aim of this study was to further investigate the faecal microbial landscape of CRC patients, with a focus on the oral pathogens Parvimonas micra and Fusobacterium nucleatum.&lt;h4>Methods&lt;/h4>In this study, 16S rRNA sequencing was conducted using faecal samples from CRC patients (n = 275) and controls without pathological findings (n = 95).&lt;h4>Results&lt;/h4>We discovered a significant difference in microbial composition depending on tumour location and microsatellite instability (MSI) status, with P. micra, F. nucleatum, and Peptostreptococcus stomatis found to be </pubmed_abstract><journal>Journal of translational medicine</journal><pagination>947</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11487773</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Parvimonas micra forms a distinct bacterial network with oral pathobionts in colorectal cancer patients.</pubmed_title><pmcid>PMC11487773</pmcid><pubmed_authors>Wai SN</pubmed_authors><pubmed_authors>Palmqvist R</pubmed_authors><pubmed_authors>Lowenmark T</pubmed_authors><pubmed_authors>Bronnec V</pubmed_authors><pubmed_authors>Larsson P</pubmed_authors><pubmed_authors>Edin S</pubmed_authors><pubmed_authors>Lofgren-Burstrom A</pubmed_authors><pubmed_authors>Zingmark C</pubmed_authors><pubmed_authors>Dahlberg M</pubmed_authors><pubmed_authors>Rosenbaum W</pubmed_authors><pubmed_authors>Schroeder BO</pubmed_authors><pubmed_authors>Ljuslinder I</pubmed_authors><pubmed_authors>Kohn L</pubmed_authors><pubmed_authors>Kellgren T</pubmed_authors></additional><is_claimable>false</is_claimable><name>Parvimonas micra forms a distinct bacterial network with oral pathobionts in colorectal cancer patients.</name><description>&lt;h4>Background&lt;/h4>Mounting evidence suggests a significant role of the gut microbiota in the development and progression of colorectal cancer (CRC). In particular, an over-representation of oral pathogens has been linked to CRC. The aim of this study was to further investigate the faecal microbial landscape of CRC patients, with a focus on the oral pathogens Parvimonas micra and Fusobacterium nucleatum.&lt;h4>Methods&lt;/h4>In this study, 16S rRNA sequencing was conducted using faecal samples from CRC patients (n = 275) and controls without pathological findings (n = 95).&lt;h4>Results&lt;/h4>We discovered a significant difference in microbial composition depending on tumour location and microsatellite instability (MSI) status, with P. micra, F. nucleatum, and Peptostreptococcus stomatis found to be </description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Oct</publication><modification>2025-04-04T19:45:38.293Z</modification><creation>2025-04-04T19:45:38.293Z</creation></dates><accession>S-EPMC11487773</accession><cross_references><pubmed>39420333</pubmed><doi>10.1186/s12967-024-05720-8</doi></cross_references></HashMap>