AI Article Synopsis

  • The study explores the relationship between the microbiome and host transcriptomes in oral squamous cell carcinoma (OSCC) using advanced techniques beyond traditional 16S rRNA gene sequencing.
  • Analysis of tissue samples and healthy controls revealed a unique microbiome in OSCC that is low in abundance yet active, with specific bacteria and bacteriophages linked to cancer-related gene expression.
  • Findings suggest that interactions between the microbiome and host may contribute to oral cancer development, highlighting the need for further experimental validation of these mechanisms.

Article Abstract

Unlabelled: Studies on the microbiome of oral squamous cell carcinoma (OSCC) have been limited to 16S rRNA gene sequencing. Here, laser microdissection coupled with brute-force, deep metatranscriptome sequencing was employed to simultaneously characterize the microbiome and host transcriptomes and predict their interaction in OSCC. The analysis involved 20 HPV16/18-negative OSCC tumor/adjacent normal tissue pairs (TT and ANT) along with deep tongue scrapings from 20 matched healthy controls (HC). Standard bioinformatic tools coupled with in-house algorithms were used to map, analyze, and integrate microbial and host data. Host transcriptome analysis identified enrichment of known cancer-related gene sets, not only in TT versus ANT and HC, but also in the ANT versus HC contrast, consistent with field cancerization. Microbial analysis identified a low abundance yet transcriptionally active, unique multi-kingdom microbiome in OSCC tissues predominated by bacteria and bacteriophages. HC showed a different taxonomic profile yet shared major microbial enzyme classes and pathways with TT/ANT, consistent with functional redundancy. Key taxa enriched in TT/ANT compared with HC were , , Human Herpes Virus 6B, and bacteriophage Yuavirus. Functionally, hyaluronate lyase was overexpressed by in TT/ANT. Microbiome-host data integration revealed that OSCC-enriched taxa were associated with upregulation of proliferation-related pathways. In a preliminary validation experiment, infection of SCC25 oral cancer cells with resulted in upregulation of MYC expression. The study provides a new insight into potential mechanisms by which the microbiome can contribute to oral carcinogenesis, which can be validated in future experimental studies.

Significance: Studies have shown that a distinct microbiome is associated with OSCC, but how the microbiome functions within the tumor interacts with the host cells remains unclear. By simultaneously characterizing the microbial and host transcriptomes in OSCC and control tissues, the study provides novel insights into microbiome-host interactions in OSCC which can be validated in future mechanistic studies.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10166004PMC
http://dx.doi.org/10.1158/2767-9764.CRC-22-0349DOI Listing

Publication Analysis

Top Keywords

microbiome-host interactions
8
oral squamous
8
squamous cell
8
cell carcinoma
8
host transcriptomes
8
microbial host
8
analysis identified
8
validated future
8
oscc
7
microbiome
6

Similar Publications

Host-microbiome-dietary interactions play crucial roles in regulating human health, yet their direct functional assessment remains challenging. We adopted metagenome-informed metaproteomics (MIM), in mice and humans, to non-invasively explore species-level microbiome-host interactions during commensal and pathogen colonization, nutritional modification, and antibiotic-induced perturbation. Simultaneously, fecal MIM accurately characterized the nutritional exposure landscape in multiple clinical and dietary contexts.

View Article and Find Full Text PDF

Microbiome-animal host symbioses are ubiquitous in nature. Animal-associated microbiomes can play a crucial role in host physiology, health and resilience to environmental stressors. As climate change drives rising global temperatures and increases the frequency of thermal extremes, microbiomes are emerging as a new frontier in buffering vulnerable animals against temperature fluctuations.

View Article and Find Full Text PDF

Charting the microbial frontier: a comprehensive guidebook for advancing microbiome research.

FEMS Microbiol Rev

January 2025

Division of Biomaterial and Biomedical Sciences, Oregon Health & Science University, School of Dentistry, Portland, OR 97239,  United States.

Specific microbial pathogens have evolved the capacity to sense immune mediators and use these signals to adapt and prepare against an incoming immune attack.

View Article and Find Full Text PDF

binary toxin CDT induces biofilm-like persisting microcolonies.

Gut Microbes

December 2025

Pathogenesis of Bacterial Anaerobes, Department of Microbiology, Institut Pasteur, Université Paris-Cité, UMR-CNRS 6047, Paris, France.

Clinical symptoms of infection (CDI) range from diarrhea to pseudomembranous colitis. A major challenge in managing CDI is the high rate of relapse. Several studies correlate the production of CDT binary toxin by clinical strains of with higher relapse rates.

View Article and Find Full Text PDF

Bibliometric and visual analysis of human microbiome-breast cancer interactions: current insights and future directions.

Front Microbiol

December 2024

Department of Breast Surgery and Institutes for Systems Genetics, Frontiers Science Center for Disease-Related Molecular Network, West China Hospital, Sichuan University, Sichuan, China.

The composition of the gut microbiome differs from that of healthy individuals and is closely linked to the progression and development of breast cancer. Recent studies have increasingly examined the relationship between microbial communities and breast cancer. This study analyzed the research landscape of microbiome and breast cancer, focusing on 736 qualified publications from the Web of Science Core Collection (WoSCC).

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!