Department of Veterinary and Biomedical Sciences and The Center for Molecular Toxicology and Carcinogenesis, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Toxicol Sci. 2010 Jan;113(1):27-36. doi: 10.1093/toxsci/kfp212. Epub 2009 Sep 11.
Ligand activation of peroxisome proliferator-activated receptor (PPAR)-beta/delta and inhibition of cyclooxygenase-2 (COX-2) activity by nonsteroidal anti-inflammatory drugs can attenuate skin tumorigenesis. There is also evidence that attenuation of skin tumorigenesis by inhibition of COX-2 activity occurs through PPARbeta/delta-independent mechanisms. The present study examined the hypothesis that combining ligand activation of PPARbeta/delta with inhibition of COX-2 activity will cooperatively inhibit chemically induced skin tumor progression using both in vivo and ex vivo models. A two-stage chemical carcinogenesis bioassay was performed in wild-type and Pparbeta/delta-null mice. After 22 weeks, cohorts of both mouse lines were divided into four experimental groups: (1) control, (2) topical application of the PPARbeta/delta ligand GW0742, (3) dietary administration of the COX-2 inhibitor nimesulide, or (4) both GW0742 and nimesulide. Ligand activation of PPARbeta/delta did not influence skin tumor progression, while a modest decrease in skin tumor multiplicity was observed with dietary nimesulide. Interestingly, the combined treatment of GW0742 and nimesulide increased the efficacy of the decrease in papilloma multiplicity for 6 weeks in wild-type mice, but this effect was not found at later time points and was not found in similarly treated Pparbeta/delta-null mice. Neoplastic keratinocyte lines cultured with GW0742 and nimesulide also exhibited enhanced inhibition of cell proliferation coincident with increased expression of Keratin messenger RNAs. Results from these studies support the hypothesis that combining ligand activation of PPARbeta/delta with inhibition of COX-2 activity can inhibit chemically induced skin tumor progression by modulating differentiation.
配体激活过氧化物酶体增殖物激活受体 (PPAR)-β/δ 和非甾体抗炎药抑制环氧化酶-2 (COX-2) 活性可减轻皮肤肿瘤的发生。也有证据表明 COX-2 活性抑制通过 PPARβ/δ 非依赖性机制发生。本研究通过体内和体外模型检验了以下假设:通过激活 PPARβ/δ 配体与抑制 COX-2 活性相结合,将协同抑制化学诱导的皮肤肿瘤进展。在野生型和 Pparβ/δ 缺陷型小鼠中进行了两阶段化学致癌生物测定。22 周后,将两种小鼠系的队列分为四个实验组:(1) 对照组,(2) 局部应用 PPARβ/δ 配体 GW0742,(3) 饮食给予 COX-2 抑制剂尼美舒利,或(4) GW0742 和尼美舒利联合应用。PPARβ/δ 配体的激活并不影响皮肤肿瘤的进展,而饮食尼美舒利则观察到皮肤肿瘤多发性略有降低。有趣的是,GW0742 和尼美舒利联合治疗在 6 周内增加了野生型小鼠中多发性肿瘤减少的疗效,但在后期时间点未发现这种效果,并且在接受类似治疗的 Pparβ/δ 缺陷型小鼠中也未发现这种效果。用 GW0742 和尼美舒利培养的肿瘤角质形成细胞系也表现出细胞增殖的抑制增强,同时 Keratin 信使 RNA 的表达增加。这些研究的结果支持以下假设:通过调节分化,将 PPARβ/δ 配体的激活与 COX-2 活性的抑制相结合,可抑制化学诱导的皮肤肿瘤进展。