Table 3.
Gut Microbiota Involved with Epigenetic Alterations in CRC
| Epigenetic modification | Microbiota studied | Model | Key findings | REFs |
|---|---|---|---|---|
| Methylation | Murine gut microbiota | GF mice | The methylation of WIF1, PENK, and NPY were associated with CRC dysbiosis. | [94] |
| Murine gut microbiota | Lgr5-EGFP-CreER mice | Gene methylation was increased by microbiota transplantation. | [148] | |
| L. acidophilus, B. infantis, and Klebsiella species | Human intestinal epithelial cells (IECs) | Microbiota treatment resulted in differential methylation changes in 200 regions of DNA. | [149] | |
| Murine gut microbiota | GF mice | The number of changes in the methylation status of genes increased with age of GF mice. | [150] | |
| ETBF | MinApcΔ716+/− mice | ETBF-induced tumors contained methylated tumor suppressor genes. | [151] | |
| Histone modifications | Murine gut microbiota | wild-type mice | Histone marks H3K4me1 and H3K27ac were enriched at poised or active enhancers. | [152] |
| Antibiotic-treated murine microbiota | GF mice | De novo generation of oscillating histone marks and rhythmically expressed genes. | [153] | |
| Murine gut microbiota | wild-type mice | Bacterial presence resulted in numerous changes in histone acetylation in the proximal colon tissue. | [154] | |
| Murine gut microbiota | GF mice | The location of H3K4 methylation marks was modified when gut microbes colonized. | [155] | |
| Antibiotic-treated murine microbiota | GF mice | Derived SCFAs promoted H3K18 crotonylation by inhibiting HDACs. | [156] | |
| Non-coding RNAs | E. coli strains or fecal-derived murine microbiota | GF mice | Distinct changes in lncRNA signatures occurred after GF mice were reconstituted with normal mouse microbiota or with E. coli alone. | [105] |
| F. nucleatum | CRC xenograft model | F. nucleatum caused resistance to oxaliplatin and 5-FU via downregulation of miR-4802 and miR-18a. | [108] | |
| Murine gut microbiota | GF mice | A total of 19 miRNAs in IESCs significantly differed in expression depending on microbial status. | [157] | |
| Murine gut microbiota | GF mice | Microbiota-dependent miR-21–5p expression in IECs regulated intestinal epithelial permeability via ARF4. | [107] | |
| Antibiotic-treated murine microbiota | GF mice | miRNAs let-7b, miR-141, and miR-200a expression were significantly reduced in GF mice. | [106] | |
| Murine gut microbiota | IEC-miRNA-deficient mice | The presence of gut microbes was associated with decreased production of miRNAs. | [158] |