Issue 4, 2023

Multi-omics insights into the interplay between gut microbiota and colorectal cancer in the “microworld” age

Abstract

Colorectal cancer (CRC) is a multifactorial heterogeneous disease largely due to both genetic predisposition and environmental factors including the gut microbiota, a dynamic microbial ecosystem inhabiting the gastrointestinal tract. Elucidation of the molecular mechanisms by which the gut microbiota interacts with the host may contribute to the pathogenesis, diagnosis, and promotion of CRC. However, deciphering the influence of genetic variants and interactions with the gut microbial ecosystem is rather challenging. Despite recent advancements in single omics analysis, the application of multi-omics approaches to integrate multiple layers of information in the microbiome and host to introduce effective prevention, diagnosis, and treatment strategies is still in its infancy. Here, we integrate host- and microbe-based multi-omics studies, respectively, to provide a strategy to explore potential causal relationships between gut microbiota and colorectal cancer. Specifically, we summarize the recent multi-omics studies such as metagenomics combined with metabolomics and metagenomics combined with genomics. Meanwhile, the sample size and sample types commonly used in multi-omics research, as well as the methods of data analysis, were also generalized. We highlight multiple layers of information from multi-omics that need to be verified by different types of models. Together, this review provides new insights into the clinical diagnosis and treatment of colorectal cancer patients.

Graphical abstract: Multi-omics insights into the interplay between gut microbiota and colorectal cancer in the “microworld” age

Article information

Article type
Review Article
Submitted
25 Oct 2022
Accepted
14 Feb 2023
First published
16 Feb 2023

Mol. Omics, 2023,19, 283-296

Multi-omics insights into the interplay between gut microbiota and colorectal cancer in the “microworld” age

A. Wang, D. Song, Y. Hong and N. Liu, Mol. Omics, 2023, 19, 283 DOI: 10.1039/D2MO00288D

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