Molecular Hematopathology Laboratory, Department of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY 10065, USA.
PPAR Res. 2008;2008:209629. doi: 10.1155/2008/209629.
The role of PPARgamma in tumorigenesis is controversial. In this article, we review and analyze literature from the past decade that highlights the potential proneoplastic activity of PPARgamma. We discuss the following five aspects of the nuclear hormone receptor and its agonists: (1) relative expression of PPARgamma in human tumor versus normal tissues; (2) receptor-dependent proneoplastic effects; (3) impact of PPARgamma and its agonists on tumors in animal models; (4) clinical trials of thiazolidinediones (TZDs) in human malignancies; (5) TZDs as chemopreventive agents in epidemiology studies. The focus is placed on the most relevant in vivo animal models and human data. In vitro cell line studies are included only when the effects are shown to be dependent on the PPARgamma receptor.
PPARγ 在肿瘤发生中的作用存在争议。在本文中,我们回顾和分析了过去十年的文献,这些文献强调了 PPARγ 潜在的致癌活性。我们讨论了核激素受体及其激动剂的以下五个方面:(1)PPARγ 在人肿瘤与正常组织中的相对表达;(2)受体依赖性致癌作用;(3)PPARγ 及其激动剂对动物模型中肿瘤的影响;(4)噻唑烷二酮(TZDs)在人类恶性肿瘤中的临床试验;(5)流行病学研究中 TZDs 作为化学预防剂。重点放在最相关的体内动物模型和人体数据上。只有当细胞系研究的作用依赖于 PPARγ 受体时,才会包含体外细胞系研究。