Department of Nutrition, The Second School of Clinical Medicine, Nanjing University of Chinese Medicine, Nanjing 210023, China; Department of Nutrition and Food Safety, School of Public Health, Nanjing Medical University, Nanjing 211166, China.
Department of Nutrition and Food Safety, School of Public Health, Nanjing Medical University, Nanjing 211166, China.
Environ Toxicol Pharmacol. 2018 Oct;63:29-33. doi: 10.1016/j.etap.2018.08.007. Epub 2018 Aug 13.
Prostate cancer is one of the most commonly diagnosed cancers in man. Studies have shown that phthalates may act as promoters in various types of cancer; however, the role of phthalates in prostate cancer has been rarely reported. The MAPK/AP-1 pathway is a vital regulator of cell proliferation in cancer. In this report we found that three typical phthalates, diethylhexyl phthalate (DEHP), Butyl benzyl phthalate (BBP) and Dibutyl phthalate (DBP), up-regulated cyclinD1 and PCNA, down-regulated P21, inducing proliferation of prostate cancer cells. Furthermore, we found that phthalates increased the expression of p-ERK5 and p-p38, along with upregulation of AP-1 (p-c-fos and p-c-jun). In studies with ERK5 and a p38 inhibitor, our data showed that downregulation of p-ERK5 or p38 inhibited phthalate-triggered cell proliferation. Taken together, findings from this study suggest that phthalates activate MAPK/AP-1 pathway and may potentially promote cell proliferation in prostate cancer, thus providing new insight into the effects and the underlying mechanism of phthalates on prostate cancer.
前列腺癌是男性最常见的癌症之一。研究表明,邻苯二甲酸酯可能作为各种类型癌症的促进剂;然而,邻苯二甲酸酯在前列腺癌中的作用却鲜有报道。MAPK/AP-1 通路是癌症中细胞增殖的重要调节剂。在本报告中,我们发现三种典型的邻苯二甲酸酯,邻苯二甲酸二乙酯(DEHP)、邻苯二甲酸丁基苄基酯(BBP)和邻苯二甲酸二丁酯(DBP),上调了细胞周期蛋白 D1 和 PCNA,下调了 P21,诱导前列腺癌细胞增殖。此外,我们发现邻苯二甲酸酯增加了 p-ERK5 和 p-p38 的表达,同时上调了 AP-1(p-c-fos 和 p-c-jun)。在使用 ERK5 和 p38 抑制剂的研究中,我们的数据表明,下调 p-ERK5 或 p38 抑制了邻苯二甲酸酯触发的细胞增殖。综上所述,这项研究的结果表明,邻苯二甲酸酯激活了 MAPK/AP-1 通路,并可能潜在地促进前列腺癌细胞增殖,从而为邻苯二甲酸酯对前列腺癌的作用和潜在机制提供了新的见解。