Abstract
Before the discovery of peroxisome proliferator activated receptors (PPARs), it
was well known that certain drugs considered as classical PPAR-alpha agonists
induced hepatocarcinoma or peroxisome proliferation in rodents. These drugs were
derivatives of fibric acid, and they included clofibrate, bezafibrate, and
fenofibrate. However, such toxicity has never been observed in human patients
treated with these hypolipidemic drugs. Thiazolidinediones are a new class of
PPAR activators showing greater specificity for the gamma isoform of PPARs. These
drugs are used as insulin sensitizers in the treatment of type II diabetes. In
addition, they have been shown to induce cell differentiation or apoptosis in
various experimental models of cancer. PPAR-alpha ligands have also been shown to
induce cancer cell differentiation and, paradoxically, PPAR-gamma drug activators
have been reported to act as carcinogens. The confusing picture that emerges from
these data is further complicated by the series of intriguing side effects
observed following administration of pharmacological PPAR ligands
(rhabdomyolysis, liver and heart toxicity, anemia, leucopenia). These side
effects cannot be easily explained by simple interactions between the drug and
nuclear receptors. Rather, these side effects seem to indicate that the ligands
have biological activity independent of the nuclear receptors. Considering the
emerging role of mitochondria in cancer and the potential metabolic connections
between this organelle and PPAR physiology, characterization of the reciprocal
influences is fundamental not only for a better understanding of cancer biology,
but also for more defined pharmacotoxicological profiles of drugs that modulate
PPARs.
Lingua originale | English |
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pagine (da-a) | 1687-1697 |
Numero di pagine | 11 |
Rivista | PPAR Research |
Stato di pubblicazione | Pubblicato - 2008 |
Keywords
- PPAR
- cancer
- cell differentiation
- mitochondria