Yu Jun, Leung Wai K, Chen Jie, Ebert Matthias P A, Malfertheiner Peter, Sung Joseph J Y
Department of Medicine and Therapeutics, Prince of Wales Hospital, The Chinese University of Hong Kong, 30-32 Ngan Shing Street, Shatin, Hong Kong, China.
Cancer Lett. 2005 Jun 1;223(1):11-7. doi: 10.1016/j.canlet.2004.09.052.
Peroxisome proliferator-activated receptor delta (PPARdelta) is ligand-activated transcription factor of the nuclear receptor superfamily which is recently implicated in carcinogenesis. We examined the expression profiles of PPARdelta in human gastric cancer, normal gastric mucosa and gastric cancer cell lines by RT-PCR, Western blot and immunohistochemistry. PPARdelta mRNA and protein was found to be ubiquitously expressed in all 5 gastric cancer cell lines, 40 gastric cancer samples and 10 normal gastric mucosa from non-cancer patients. Positive immunoreactivity was detected in the nuclei of normal and malignant gastric epithelium. Treatment of gastric cell line MKN45 that overexpressed cyclooxygenase-2 (COX-2) with specific COX-2 inhibitor NS398 resulted in a time- and dose-dependent suppression of PPARdelta expression. In contrast, there was no suppression of PPARdelta in MKN28 gastric cell line with low COX-2 expression. Our results demonstrated the ubiquitous expression of PPARdelta in normal and cancer gastric epithelium. Suppression of PPARdelta may be one of the mechanisms underlying the chemopreventive effects of COX-2 inhibitor.
过氧化物酶体增殖物激活受体δ(PPARδ)是核受体超家族的一种配体激活转录因子,最近被认为与肿瘤发生有关。我们通过逆转录聚合酶链反应(RT-PCR)、蛋白质免疫印迹法和免疫组织化学法检测了PPARδ在人胃癌、正常胃黏膜及胃癌细胞系中的表达情况。结果发现,PPARδ的信使核糖核酸(mRNA)和蛋白质在所有5种胃癌细胞系、40份胃癌样本以及10份来自非癌症患者的正常胃黏膜中均有广泛表达。在正常和恶性胃上皮细胞核中均检测到阳性免疫反应性。用特异性环氧化酶-2(COX-2)抑制剂NS398处理过表达COX-2的胃癌细胞系MKN45,可导致PPARδ表达呈时间和剂量依赖性抑制。相比之下,COX-2表达较低的MKN28胃癌细胞系中PPARδ未受到抑制。我们的结果表明PPARδ在正常和癌性胃上皮中均有广泛表达。PPARδ的抑制可能是COX-2抑制剂化学预防作用的潜在机制之一。