4.7 Review

Emerging role of trimethylamine-N-oxide (TMAO) in colorectal cancer

Journal

APPLIED MICROBIOLOGY AND BIOTECHNOLOGY
Volume 105, Issue 20, Pages 7651-7660

Publisher

SPRINGER
DOI: 10.1007/s00253-021-11582-7

Keywords

Colorectal cancer; TMAO; Gut microbiota; Oxidative stress; DNA damage

Funding

  1. SERB-DST [CRG/2018/002957]
  2. Core grant of the National Institute of Immunology, New Delhi, India
  3. Department of Biotechnology for Indo-Russia [DBT/IC-2/Indo-Russia/2017-19/02]
  4. Indian Council of Medical Research (ICMR), India [34/13/2019-TF/Nano/BMS]

Ask authors/readers for more resources

TMAO, a metabolite derived from gut microbiota, has attracted attention for its potential role in colorectal cancer carcinogenesis, but lacks empirical mechanistic evidence. This review discusses possible mechanisms of TMAO in CRC, emphasizing the need for further mechanistic studies to solidify the link between TMAO and CRC causation.
Among gut microbiota-derived metabolites, trimethylamine-N-oxide (TMAO) is receiving increased attention due to its possible role in the carcinogenesis of colorectal cancer (CRC). In spite of numerous reports implicating TMAO with CRC, there is a lack of empirical mechanistic evidences to concretize the involvement of TMAO in the carcinogenesis of CRC. Possible mechanisms such as inflammation, oxidative stress, DNA damage, and protein misfolding by TMAO have been discussed in this review in the light of the latest advancements in the field. This review is an attempt to discuss the probable correlation between TMAO and CRC but this linkage can be concretized only once we get sufficient empirical evidences from the mechanistic studies. We believe, this review will augment the understanding of linking TMAO with CRC and will motivate researchers to move towards mechanistic study for reinforcing the idea of implicating TMAO with CRC causation.

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