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. Author manuscript; available in PMC: 2022 Jan 1.
Published in final edited form as: Biochim Biophys Acta Rev Cancer. 2020 Dec 13;1875(1):188490. doi: 10.1016/j.bbcan.2020.188490

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]