Department of Medicine, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
PPAR Res. 2008;2008:931074. doi: 10.1155/2008/931074.
The peroxisome proliferator-activated receptors (PPARs) are members of the nuclear hormone receptor superfamily. These receptors are also ligand-dependent transcription factors responsible for the regulation of cellular events that range from glucose and lipid homeostases to cell differentiation and apoptosis. The importance of these receptors in lipid homeostasis and energy balance is well established. In addition to these metabolic and anti-inflammatory properties, emerging evidence indicates that PPARs can function as either tumor suppressors or accelerators, suggesting that these receptors are potential candidates as drug targets for cancer prevention and treatment. However, conflicting results have emerged regarding the role of PPARs on colon carcinogenesis. Therefore, further investigation is warranted prior to considering modulation of PPARs as an efficacious therapy for colorectal cancer chemoprevention and treatment.
过氧化物酶体增殖物激活受体(PPARs)是核激素受体超家族的成员。这些受体也是配体依赖性转录因子,负责调节从葡萄糖和脂质稳态到细胞分化和细胞凋亡等细胞事件。这些受体在脂质稳态和能量平衡中的重要性已得到充分证实。除了这些代谢和抗炎特性外,新出现的证据表明,PPARs 可以作为肿瘤抑制剂或促进剂发挥作用,这表明这些受体是预防和治疗癌症的潜在药物靶点。然而,关于 PPARs 在结肠癌发生中的作用,已经出现了相互矛盾的结果。因此,在考虑将 PPAR 作为结直肠癌化学预防和治疗的有效治疗方法之前,有必要进行进一步的研究。