Laboratory of Molecular Pharmacology; Department of Oncology; IRCCS-Istituto di Ricerche Farmacologiche Mario Negri; Milan, Italy.
Epigenetics. 2013 Jun;8(6):656-65. doi: 10.4161/epi.24916. Epub 2013 Jun 14.
Brostallicin is a DNA minor groove binder that shows enhanced antitumor activity in cells with high glutathione S-transferase (GST)/glutathione content. Prostate cancer cells present, almost invariably, methylation of the GSTP1 gene promoter and, as a consequence, low levels of GST-pi expression and activity. In these cells, brostallicin shows very little activity. We tested whether pretreatment of heavily GST-methylated prostate cancer cells with demethylating agents could enhance the activity of brostallicin. Human prostate cancer cells LNCaP and DU145 were used for these studies both in vitro and in vivo. The demethylating agent zebularine was used in combination with brostallicin. Methylation specific PCR and pyrosequencing were used to determine the level of GST methylation. Pretreatment with demethylating agents enhanced the in vitro activity of brostallicin in LNCaP cells. Zebularine, in particular, induced an enhancement of activity in vivo comparable to that obtained by transfecting the human GSTP1 gene in LNCaP cells in vitro. Molecular analysis performed on tumor xenografts in mice pretreated with zebularine failed to detect re-expression of GST-pi and demethylation of GSTP1. However, we found demethylation in the GSTM1 gene, with consequent re-expression of GST-mu at the mRNA level. These results indicate that zebularine, both in vitro and in vivo, enhances the activity of brostallicin and that this enhancement correlates with re-expression of GST-pi and GST-mu. These findings highlight the potential therapeutic value of combining demethylating agents and brostallicin in tumors with GST methylation that poorly respond to brostallicin.
布罗他丁是一种 DNA 小沟结合物,在谷胱甘肽 S-转移酶 (GST)/谷胱甘肽含量高的细胞中显示出增强的抗肿瘤活性。前列腺癌细胞几乎总是存在 GSTP1 基因启动子的甲基化,因此 GST-π表达和活性水平较低。在这些细胞中,布罗他丁的活性非常低。我们测试了先用去甲基化剂预处理高度 GST 甲基化的前列腺癌细胞是否可以增强布罗他丁的活性。我们在体外和体内使用人前列腺癌细胞 LNCaP 和 DU145 进行这些研究。使用去甲基化剂 zebularine 与布罗他丁联合使用。甲基化特异性 PCR 和焦磷酸测序用于确定 GST 甲基化水平。用去甲基化剂预处理可增强 LNCaP 细胞中布罗他丁的体外活性。特别是 zebularine 诱导了体内活性的增强,与体外转染人 GSTP1 基因在 LNCaP 细胞中获得的增强相当。用 zebularine 预处理的小鼠肿瘤异种移植进行的分子分析未能检测到 GST-π的重新表达和 GSTP1 的去甲基化。然而,我们发现 GSTM1 基因的去甲基化,导致 GST-μ在 mRNA 水平上的重新表达。这些结果表明,zebularine 无论是在体外还是体内,都能增强布罗他丁的活性,这种增强与 GST-π和 GST-μ的重新表达相关。这些发现强调了在 GST 甲基化的肿瘤中联合使用去甲基化剂和布罗他丁的潜在治疗价值,这些肿瘤对布罗他丁反应不佳。