Department of Histology and Embryology, Poznan University of Medical Sciences, PL-61-781 Poznan, Poland.
Int J Mol Sci. 2020 Apr 9;21(7):2619. doi: 10.3390/ijms21072619.
Ovarian cancer rates the highest mortality among all gynecological malignancies. The main reason for high mortality is the development of drug resistance. It can be related to increased expression of drug transporters and increased expression of extracellular matrix (ECM) proteins. Our foremost aim was to exhibit alterations in the miRNA expression levels in cisplatin (CIS), paclitaxel (PAC), doxorubicin (DOX), and topotecan (TOP)-resistant variants of the W1 sensitive ovarian cancer cell line-using miRNA microarray. The second goal was to identify miRNAs responsible for the regulation of drug-resistant genes. According to our observation, alterations in the expression of 40 miRNAs were present. We could observe that, in at least one drug-resistant cell line, the expression of 21 miRNAs was upregulated and that of 19 miRNAs was downregulated. We identified target genes for 22 miRNAs. Target analysis showed that miRNA regulates key genes responsible for drug resistance. Among others, we observed regulation of the ATP-binding cassette subfamily B member 1 gene () in the paclitaxel-resistant cell line by miR-363 and regulation of the collagen type III alpha 1 chain gene () in the topotekan-resistant cell line by miR-29a.
卵巢癌是妇科恶性肿瘤中死亡率最高的。死亡率高的主要原因是耐药性的发展。这可能与药物转运蛋白表达增加和细胞外基质 (ECM) 蛋白表达增加有关。我们的首要目标是使用 miRNA 微阵列展示顺铂 (CIS)、紫杉醇 (PAC)、多柔比星 (DOX) 和拓扑替康 (TOP) 耐药变体中 miRNA 表达水平的变化在 W1 敏感卵巢癌细胞系中。第二个目标是确定负责调节耐药基因的 miRNAs。根据我们的观察,有 40 个 miRNA 的表达发生了改变。我们可以观察到,在至少一种耐药细胞系中,21 个 miRNA 的表达上调,19 个 miRNA 的表达下调。我们确定了 22 个 miRNA 的靶基因。靶基因分析表明,miRNA 调节耐药的关键基因。其中,我们观察到 miR-363 对紫杉醇耐药细胞系中的 ATP 结合盒亚家族 B 成员 1 基因 () 的调节,以及 miR-29a 对拓扑替康耐药细胞系中的 III 型胶原 α 1 链基因 () 的调节。