Boitier Eric, Gautier Jean-Charles, Roberts Ruth
Aventis Pharma Drug Safety Evaluation, Centre de Recherche de Paris, 13 Quai Jules Guesde 94403, Vitry sur Seine, Paris, France.
Comp Hepatol. 2003 Jan 31;2(1):3. doi: 10.1186/1476-5926-2-3.
Peroxisome proliferator activated receptors (PPARs) are a family of related receptors implicated in a diverse array of biological processes. There are 3 main isotypes of PPARs known as PPARalpha, PPARbeta and PPARgamma and each is organized into domains associated with a function such as ligand binding, activation and DNA binding. PPARs are activated by ligands, which can be both endogenous such as fatty acids or their derivatives, or synthetic, such as peroxisome proliferators, hypolipidaemic drugs, anti-inflammatory or insulin-sensitizing drugs. Once activated, PPARs bind to DNA and regulate gene transcription. The different isotypes differ in their expression patterns, lending clues on their function. PPARalpha is expressed mainly in liver whereas PPARgamma is expressed in fat and in some macrophages. Activation of PPARalpha in rodent liver is associated with peroxisome proliferation and with suppression of apoptosis and induction of cell proliferation. The mechanism by which activation of PPARalpha regulates apoptosis and proliferation is unclear but is likely to involve target gene transcription. Similarly, PPARgamma is involved in the induction of cell growth arrest occurring during the differentiation process of fibroblasts to adipocytes. However, it has been implicated in the regulation of cell cycle and cell proliferation in colon cancer models. Less in known concerning PPARbeta but it was identified as a downstream target gene for APC/beta-catenin/T cell factor-4 tumor suppressor pathway, which is involved in the regulation of growth promoting genes such as c-myc and cyclin D1. Marked species and tissue differences in the expression of PPARs complicate the extrapolation of pre-clinical data to humans. For example, PPARalpha ligands such as the hypolipidaemic fibrates have been used extensively in the clinic over the past 20 years to treat cardiovascular disease and side effects of clinical fibrate use are rare, despite the observation that these compounds are rodent carcinogens. Similarly, adverse clinical responses have been seen with PPARgamma ligands that were not predicted by pre-clinical models. Here, we consider the response to PPAR ligands seen in pre-clinical models of efficacy and safety in the context of human health and disease.
过氧化物酶体增殖物激活受体(PPARs)是一族参与多种生物学过程的相关受体。PPARs主要有3种同型体,即PPARα、PPARβ和PPARγ,每种同型体都由与配体结合、激活及DNA结合等功能相关的结构域组成。PPARs可被配体激活,这些配体既可以是内源性的,如脂肪酸或其衍生物,也可以是合成的,如过氧化物酶体增殖剂、降血脂药物、抗炎或胰岛素增敏药物。一旦被激活,PPARs就会与DNA结合并调节基因转录。不同的同型体在表达模式上存在差异,这为其功能提供了线索。PPARα主要在肝脏中表达,而PPARγ在脂肪组织和一些巨噬细胞中表达。在啮齿动物肝脏中激活PPARα与过氧化物酶体增殖、细胞凋亡抑制及细胞增殖诱导有关。PPARα激活调节细胞凋亡和增殖的机制尚不清楚,但可能涉及靶基因转录。同样,PPARγ参与成纤维细胞向脂肪细胞分化过程中发生的细胞生长停滞的诱导。然而,在结肠癌模型中,它与细胞周期和细胞增殖的调节有关。关于PPARβ的了解较少,但它被确定为APC/β-连环蛋白/T细胞因子-4肿瘤抑制途径的下游靶基因,该途径参与如c-myc和细胞周期蛋白D1等促进生长基因的调节。PPARs表达的明显种属和组织差异使得将临床前数据外推至人类变得复杂。例如,降血脂贝特类药物等PPARα配体在过去20年中已在临床上广泛用于治疗心血管疾病,尽管观察到这些化合物是啮齿动物致癌物,但临床使用贝特类药物的副作用却很少见。同样,PPARγ配体也出现了临床前模型未预测到的不良临床反应。在此,我们在人类健康和疾病的背景下考虑在临床前疗效和安全性模型中观察到的对PPAR配体的反应。