Laboratory of Clinical Pharmacokinetics, Graduate School of Pharmaceutical Sciences, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, Japan.
Laboratory of Biopharmaceutics, Faculty of Pharmacy, Takasaki University of Health and Welfare, Takasaki-shi, Gunma, Japan.
PLoS One. 2018 Jul 6;13(7):e0200015. doi: 10.1371/journal.pone.0200015. eCollection 2018.
Epithelial-to-mesenchymal transition (EMT) in cancer cells facilitates tumor progression by promoting invasion and metastasis. Snail is a transcriptional factor that induces EMT, while P-glycoprotein (P-gp) is an efflux transporter involved in anticancer drug resistance, and P-gp efflux activity is stimulated in Snail-overexpressing lung cancer cells with EMT characteristics. Since the histone deacetylase (HDAC) inhibitor entinostat (Ent) reverses EMT features, our aim in this study was to determine whether Ent also suppresses P-gp activation in Snail-induced cells. First, we confirmed that Ent treatment reduced migration activity, downregulated E-cadherin and upregulated vimentin at the mRNA level in Snail-overexpressing cells, thus inhibiting EMT. Efflux and uptake assays using rhodamine123 (Rho123), a fluorescent P-gp substrate, showed that Ent also inhibited Snail-induced activation of P-gp. Moreover, P-gp activity was more strongly inhibited by Ent in Snail-overexpressing cells than in Mock cells. When we evaluated the uptakes of Rho123 by LLC-PK1 cells and P-gp-overexpressing LLC-GA5COL150 cells, Rho123 accumulation in LLC-GA5COL150 cells was significantly decreased compared with that in LLC-PK1 cells. Coincubation with Ent had no effect on Rho123 accumulation in either of the cell lines. Thus, Ent appears to be an inhibitor, but not a substrate, of P-gp at low concentration. Our results suggest that Ent treatment might suppress not only Snail-induced cancer malignant alteration, but also P-gp-mediated multidrug resistance.
上皮间质转化(EMT)在肿瘤细胞中促进侵袭和转移,从而促进肿瘤的进展。Snail 是一种诱导 EMT 的转录因子,而 P-糖蛋白(P-gp)是一种参与抗癌药物耐药性的外排转运体,并且 EMT 特征的 Snail 过表达肺癌细胞中的 P-gp 外排活性受到刺激。由于组蛋白去乙酰化酶(HDAC)抑制剂恩替诺特(Ent)逆转 EMT 特征,因此我们在这项研究中的目的是确定 Ent 是否也抑制了 Snail 诱导的细胞中 P-gp 的激活。首先,我们证实 Ent 处理降低了 Snail 过表达细胞中的迁移活性,下调了 E-钙粘蛋白并在上调了 vimentin 的 mRNA 水平,从而抑制了 EMT。使用荧光 P-gp 底物罗丹明 123(Rho123)进行的外排和摄取测定表明,Ent 还抑制了 Snail 诱导的 P-gp 激活。此外,与 Mock 细胞相比,Ent 在 Snail 过表达细胞中更强烈地抑制了 P-gp 的活性。当我们评估 Rho123 被 LLC-PK1 细胞和 P-gp 过表达的 LLC-GA5COL150 细胞摄取时,与 LLC-PK1 细胞相比,Rho123 在 LLC-GA5COL150 细胞中的积累明显减少。与 Ent 共孵育对两种细胞系中 Rho123 的积累均无影响。因此,Ent 在低浓度下似乎是 P-gp 的抑制剂,但不是底物。我们的结果表明,Ent 处理不仅可能抑制 Snail 诱导的癌症恶性改变,而且可能抑制 P-gp 介导的多药耐药性。