Cladosporols and PPARγ: Same Gun, Same Bullet, More Targets.
Roberta RapuanoAntonella MercuriSabrina DallavalleSalvatore MoriccaAntonio LavecchiaAngelo LupoPublished in: Biomolecules (2024)
Several natural compounds have been found to act as PPARγ agonists, thus regulating numerous biological processes, including the metabolism of carbohydrates and lipids, cell proliferation and differentiation, angiogenesis, and inflammation. Recently, Cladosporols, secondary metabolites purified from the fungus Cladosporium tenuissimum , have been demonstrated to display an efficient ability to control cell proliferation in human colorectal and prostate cancer cells through a PPARγ-mediated modulation of gene expression. In addition, Cladosporols exhibited a strong anti-adipogenetic activity in 3T3-L1 murine preadipocytes, preventing their in vitro differentiation into mature adipocytes. These data interestingly point out that the interaction between Cladosporols and PPARγ, in the milieu of different cells or tissues, might generate a wide range of beneficial effects for the entire organism affected by diabetes, obesity, inflammation, and cancer. This review explores the molecular mechanisms by which the Cladosporol/PPARγ complex may simultaneously interfere with a dysregulated lipid metabolism and cancer promotion and progression, highlighting the potential therapeutic benefits of Cladosporols for human health.
Keyphrases
- insulin resistance
- cell proliferation
- gene expression
- human health
- fatty acid
- papillary thyroid
- endothelial cells
- type diabetes
- oxidative stress
- adipose tissue
- risk assessment
- induced apoptosis
- metabolic syndrome
- squamous cell
- high fat diet induced
- cardiovascular disease
- dna methylation
- cell cycle
- weight loss
- ms ms
- skeletal muscle
- squamous cell carcinoma
- pi k akt
- endoplasmic reticulum stress
- cell cycle arrest
- glycemic control
- electronic health record
- machine learning
- vascular endothelial growth factor
- childhood cancer
- deep learning
- body mass index
- signaling pathway
- pluripotent stem cells