Evidence map›Paper›PMID 38713170›Full record

ReviewBioEssays : news and reviews in molecular, cellular and developmental biology2024

Flavin-containing monooxygenase (FMO): Beyond xenobiotics.

Ajay Bhat, Faith R Carranza, Angela M Tuckowski, Scott F Leiser

Abstract readReview
In one paragraph

Review in BioEssays : news and reviews in molecular, cellular and developmental biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. FMO2 Promotes Angiogenesis via Regulation of N-Acetylornithine.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
  5. Article
  6. Rewarding touch limits lifespan through neural to intestinal signaling.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Ajay BhatMolecular & Integrative Physiology Department, University of Michigan, Ann Arbor, Michigan, USA.
Faith R CarranzaCellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan, USA.
Angela M TuckowskiCellular and Molecular Biology Program, University of Michigan, Ann Arbor, Michigan, USA.
Scott F LeiserMolecular & Integrative Physiology Department, University of Michigan, Ann Arbor, Michigan, USA.ORCID 0000-0002-8003-2955

Funding

Flavin-containing monooxygenases in endogenous metabolism and agingR01AG075061 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCOTT F LEISER · 2022 to 2026
$2.1M
Mechanisms of the cell non-autonomous dietary restriction pathwayR01AG059583 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEISER, SCOTT F · 2018 to 2022
$1.9M
Mechanisms of cell non-autonomous signaling through the hypoxic responseR01AG058717 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LEISER, SCOTT F · 2019 to 2023
$1.6M
Glenn Foundation for Medical ResearchNIA NIH HHS R01 AG058717NIA NIH HHS R01 AG059583NIA NIH HHS R01 AG075061
6 · The paper itself

Abstract

Flavin-containing monooxygenases (FMOs), traditionally known for detoxifying xenobiotics, are now recognized for their involvement in endogenous metabolism. We recently discovered that an isoform of FMO, fmo-2 in Caenorhabditis elegans, alters endogenous metabolism to impact longevity and stress tolerance. Increased expression of fmo-2 in C. elegans modifies the flux through the key pathway known as One Carbon Metabolism (OCM). This modified flux results in a decrease in the ratio of S-adenosyl-methionine (SAM) to S-adenosyl-homocysteine (SAH), consequently diminishing methylation capacity. Here we discuss how FMO-2-mediated formate production during tryptophan metabolism may serve as a trigger for changing the flux in OCM. We suggest formate bridges tryptophan and OCM, altering metabolic flux away from methylation during fmo-2 overexpression. Additionally, we highlight how these metabolic results intersect with the mTOR and AMPK pathways, in addition to mitochondrial metabolism. In conclusion, the goal of this essay is to bring attention to the central role of FMO enzymes but lack of understanding of their mechanisms. We justify a call for a deeper understanding of FMO enzyme's role in metabolic rewiring through tryptophan/formate or other yet unidentified substrates. Additionally, we emphasize the identification of novel drugs and microbes to induce FMO activity and extend lifespan.

Indexed as

Caenorhabditis elegansOxygenasesXenobioticsAnimalsCaenorhabditis elegans ProteinsHumansLongevityTryptophanCaenorhabditis elegans Proteinsdimethylaniline monooxygenase (N-oxide forming)OxygenasesTryptophanXenobiotics

Identifiers

PMID38713170
PMCPMC11447872

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.