Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI 48109, USA.
PPAR Res. 2007;2007:90289. doi: 10.1155/2007/90289.
Peroxisome proliferator-activated receptors (PPARs) are ligand-activated transcription factors belonging to the nuclear hormone receptor superfamily. Their discovery in the 1990s provided insights into the cellular mechanisms involved in the control of energy homeostasis; the regulation of cell differentiation, proliferation, and apoptosis; and the modulation of important biological and pathological processes related to inflammation, among others. Since then, PPARs have become an exciting therapeutic target for several diseases. PPARs are expressed by many tumors including lung carcinoma cells, and their function has been linked to the process of carcinogenesis in lung. Consequently, intense research is being conducted in this area with the hope of discovering new PPAR-related therapeutic targets for the treatment of lung cancer. This review summarizes the research being conducted in this area and focuses on the mechanisms by which PPARs are believed to affect lung tumor cell biology.
过氧化物酶体增殖物激活受体 (PPARs) 是配体激活的转录因子,属于核激素受体超家族。它们在 20 世纪 90 年代被发现,为控制能量平衡的细胞机制、细胞分化、增殖和凋亡的调节以及与炎症等相关的重要生物学和病理过程的调节提供了深入的了解。从那时起,PPARs 已成为多种疾病的一个令人兴奋的治疗靶点。PPARs 表达于许多肿瘤,包括肺癌细胞,其功能与肺癌的癌变过程有关。因此,该领域正在进行大量研究,希望发现新的与 PPAR 相关的治疗靶点,用于治疗肺癌。本文综述了该领域的研究进展,并重点介绍了 PPARs 影响肺肿瘤细胞生物学的机制。