Department of Anatomy and Histology, Collegium Medicum, University of Zielona Gora, Zyty 28 St., 65-046 Zielona Gora, Poland.
Department of Histology and Embryology, Poznan University of Medical Sciences, 61-781 Poznan, Poland.
Int J Mol Sci. 2022 May 23;23(10):5846. doi: 10.3390/ijms23105846.
Epithelial ovarian cancer has the highest mortality among all gynecological malignancies. The main reasons for high mortality are late diagnosis and development of resistance to chemotherapy. Resistance to chemotherapeutic drugs can result from altered expression of drug-resistance genes regulated by miRNA. The main goal of our study was to detect differences in miRNA expression levels in two doxorubicin (DOX)- and two topotecan (TOP)-resistant variants of the A2780 drug-sensitive ovarian cancer cell line by miRNA microarray. The next aim was to recognize miRNAs as factors responsible for the regulation of drug-resistance genes. We observed altered expression of 28 miRNA that may be related to drug resistance. The upregulation of miR-125b-5p and miR-935 and downregulation of miR-218-5p was observed in both DOX-resistant cell lines. In both TOP-resistant cell lines, we noted the overexpression of miR-99a-5p, miR-100-5p, miR-125b-5p, and miR-125b-2-3p and decreased expression of miR-551b-3p, miR-551b-5p, and miR-383-5p. Analysis of the targets suggested that expression of important drug-resistant genes such as the collagen type I alpha 2 chain (), protein Tyrosine Phosphatase Receptor Type K (), receptor tyrosine kinase-, Roundabout Guidance Receptor 2 (), myristoylated alanine-rich C-kinase substrate (), and the ATP-binding cassette subfamily G member 2 () can be regulated by miRNA.
上皮性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诊断较晚和对化疗耐药的发展。化疗耐药可归因于 miRNA 调节的耐药基因表达的改变。我们研究的主要目的是通过 miRNA 微阵列检测两种阿霉素 (DOX) 和两种拓扑替康 (TOP) 耐药的 A2780 药物敏感卵巢癌细胞系中 miRNA 表达水平的差异。下一步的目标是识别 miRNA 作为调节耐药基因的因素。我们观察到 28 个 miRNA 的表达发生改变,这些 miRNA 可能与耐药性有关。在两种 DOX 耐药细胞系中观察到 miR-125b-5p 和 miR-935 的上调和 miR-218-5p 的下调。在两种 TOP 耐药细胞系中,我们注意到 miR-99a-5p、miR-100-5p、miR-125b-5p 和 miR-125b-2-3p 的过表达和 miR-551b-3p、miR-551b-5p 和 miR-383-5p 的表达下调。靶基因分析表明,重要耐药基因如胶原类型 I alpha 2 链 ()、蛋白酪氨酸磷酸酶受体型 K ()、受体酪氨酸激酶-、绕路指导受体 2 ()、豆蔻酰化丙氨酸丰富 C 激酶底物 () 和 ATP 结合盒亚家族 G 成员 2 () 的表达可以受到 miRNA 的调控。