Division of Pulmonary Sciences and Critical Care Medicine, Department of Medicine, University of Colorado Denver, Aurora, CO 80045, USA.
PPAR Res. 2012;2012:362085. doi: 10.1155/2012/362085. Epub 2012 Aug 12.
Peroxisome proliferator-activated receptor-γ (PPARγ) is a member of the nuclear receptor superfamily of ligand-activated transcription factors that plays an important role in the control of gene expression linked to a variety of physiological processes, including cancer. Ligands for PPARγ include naturally occurring fatty acids and the thiazolidinedione class of antidiabetic drugs. Activation of PPARγ in a variety of cancer cells leads to inhibition of growth, decreased invasiveness, reduced production of proinflammatory cytokines, and promotion of a more differentiated phenotype. However, systemic activation of PPARγ has been reported to be protumorigenic in some in vitro systems and in vivo models. Here, we review the available data that implicate PPARγ in lung carcinogenesis and highlight the challenges of targeting PPARγ in lung cancer treatments.
过氧化物酶体增殖物激活受体-γ(PPARγ)是核受体超家族的配体激活转录因子成员,在控制与多种生理过程相关的基因表达中发挥重要作用,包括癌症。PPARγ 的配体包括天然存在的脂肪酸和噻唑烷二酮类抗糖尿病药物。在各种癌细胞中激活 PPARγ 会导致生长抑制、侵袭性降低、促炎细胞因子产生减少以及促进更分化的表型。然而,据报道,在一些体外系统和体内模型中,全身激活 PPARγ 具有致癌作用。在这里,我们回顾了表明 PPARγ 参与肺癌发生的现有数据,并强调了在肺癌治疗中靶向 PPARγ 的挑战。