# Comprehensive analysis of transcriptome and microbiome in colorectal cancer with synchronous polyp patients

## TL;DR

This study explores how gut bacteria and gene activity differ in colorectal cancer patients compared to healthy people, identifying potential markers for diagnosis and treatment.

## Contribution

The study reveals novel correlations between specific gut bacteria and host gene expression in colorectal cancer patients.

## Key findings

- CRC patients showed significant differences in gut microbiota compared to healthy controls.
- TIMP1 and BCAT1 genes were positively correlated with pathogenic bacteria like Fusobacterium nucleatum.
- Tumor-related genes TRPM4, MYBL2, and CDKN2A were upregulated and linked to specific bacterial taxa.

## Abstract

Colorectal cancer (CRC) is a prevalent and lethal malignancy, with the role of gut microbiota in its development still unclear. This study examines differences in gut microbiota between CRC patients and healthy controls and explores their association with host gene expression to identify potential diagnostic and therapeutic targets.

Fecal samples from 10 CRC patients and 13 healthy controls were subjected to 16S rRNA sequencing. Transcriptome sequencing of tumor tissues, normal mucosa, and colorectal polyps from same 10 CRC patients was performed to identify differentially expressed genes (DEGs). Pearson correlation analysis was employed to associate operational taxonomic units (OTUs) with host gene expression.

β-diversity analysis showed significant differences in microbiota between CRC patients and controls (P < 0.01). LEfSe identified 38 distinct bacterial taxa, with genera such as Bacteroides, Peptostreptococcus, and Parabacteroides being enriched in CRC patients. Transcriptome analysis uncovered 1,026 DEGs. Notably, TIMP1 and BCAT1 were positively correlated (r > 0.76, P < 0.01) with pathogenic bacteria like Fusobacterium nucleatum and Peptostreptococcus stomatis. Tumor-related genes TRPM4, MYBL2, and CDKN2A were significantly upregulated and correlated with specific bacterial taxa.

This study underscores the significant alterations in gut microbiota associated with CRC and reveals novel correlations between specific microbes and host gene expression, offering potential diagnostic markers and therapeutic targets for CRC.