Saturated Oxo Fatty Acids (SOFAs): A Previously Unrecognized Class of Endogenous Bioactive Lipids Exhibiting a Cell Growth Inhibitory Activity.
Cell Line, Tumor
Cell Proliferation
/ drug effects
Cell Survival
/ drug effects
Chromatography, High Pressure Liquid
Down-Regulation
/ drug effects
Fatty Acids
/ chemistry
Humans
Lipids
/ chemistry
Mass Spectrometry
Oxidation-Reduction
Proto-Oncogene Proteins c-myc
/ genetics
STAT3 Transcription Factor
/ genetics
Stearic Acids
/ analysis
Journal
Journal of medicinal chemistry
ISSN: 1520-4804
Titre abrégé: J Med Chem
Pays: United States
ID NLM: 9716531
Informations de publication
Date de publication:
13 05 2021
13 05 2021
Historique:
pubmed:
22
4
2021
medline:
17
6
2021
entrez:
21
4
2021
Statut:
ppublish
Résumé
The discovery of novel bioactive lipids that promote human health is of great importance. Combining "suspect" and targeted lipidomic liquid chromatography-high-resolution mass spectrometry (LC-HRMS) approaches, a previously unrecognized class of oxidized fatty acids, the saturated oxo fatty acids (SOFAs), which carry the oxo functionality at various positions of the long chain, was identified in human plasma. A library of SOFAs was constructed, applying a simple green photochemical hydroacylation reaction as the key synthetic step. The synthesized SOFAs were studied for their ability to inhibit in vitro the cell growth of three human cancer cell lines. Four oxostearic acids (OSAs) were identified to inhibit the cell growth of human lung carcinoma A549 cells. 6OSA and 7OSA exhibited the highest cell growth inhibitory potency, suppressing the expression of both STAT3 and c-myc, which are critical regulators of cell growth and proliferation. Thus, naturally occurring SOFAs may play a role in the protection of human health.
Identifiants
pubmed: 33881857
doi: 10.1021/acs.jmedchem.0c02058
doi:
Substances chimiques
Fatty Acids
0
Lipids
0
Proto-Oncogene Proteins c-myc
0
STAT3 Transcription Factor
0
STAT3 protein, human
0
Stearic Acids
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM