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Analysis of the Differences in the Expression of mRNAs and miRNAs Associated with Drug Resistance in Endometrial Cancer Cells Treated with Salinomycin

机译:盐霉素治疗子宫内膜癌细胞耐药性耐药性和MIRNA表达的差异分析

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Background: It is important to understand the molecular mechanisms involved in cancer drug resistance and to study the activity of new drugs, e.g. salinomycin.Objective: The purpose of the study was to analyze changes in the expression of genes associated with drug resistance in the Ishikawa endometrial cancer cell line when treated with salinomycin. In addition, changes in the level of miRNA potentially regulating these mRNAs were evaluated.Materials and Methods: Endometrial cancer cells were treated with 1 mu M of salinomycin for 12, 24 and 48 hours periods. Untreated cells were a control culture. The molecular analysis consists of mRNA and miRNA microarray analysis and the RTqPCR technique.Results: The following was observed about the number of mRNAs differentiating the cell culture exposed to the drug compared to a control culture: H-12 vs. C - 9 mRNAs, H_24 vs. C - 6 mRNAs, and H_48 vs. C - 1 mRNA. It was noted that 4 of the 9 differentiating mRNAs were characteristic for 12 hours of exposure to salinomycin and they correspond to the following genes: TUFT1, ABCB1, MTMR11, and MX2. After 24 hours, 2 mRNAs were characteristic for this time of incubation cells with salinomycin: TUFT1 and MYD88 and after 48 hours, SLC30A5 could also be observed.Discussion: The highest differences in expression were indicated for TUFT1, MTMR11, and SLC30A5. The highest influence probability was determined between TUFT1 and hsa-miR-3188 (FC + 2.48), MTMR11 and has-miR-16 (FC-1.74), and between SLC30A5 and hsa-miR-30d (FC-2.01).Conclusion: Salinomycin induces changes in the activity of mRNA and miRNA participating in drug resistance; however, the observed changes in character are the expected result of anti-cancer treatment.
机译:背景:了解患有癌症耐药性和研究新药活性的分子机制非常重要,例如, SALINOMYCIN.OBJECTIVE:研究的目的是在用盐霉素处理时分析与Ishikawa子宫内膜癌细胞系中的耐药性相关的基因的变化。此外,评估可能调节这些mRNA的miRNA水平的变化。材料和方法:将子宫内膜癌细胞用1μm盐霉素治疗12,24和48小时。未处理的细胞是对照培养。分子分析由mRNA和miRNA微阵列分析和RTQPCR技术组成。结果:与对照培养相比,将接种细胞培养物的MRNA的数量分化为将暴露于药物暴露于药物的细胞培养物的数量:H-12与C-9 mRNA, H_24与C-6 mRNA和H_48与C - 1 mRNA。注意到,9种不同的MRNA中的4个分化的MRNA是暴露于蝾螈的12小时,它们对应于以下基因:TUFT1,ABCB1,MTMR11和MX2。 24小时后,2 mRNA是含有生理酶霉素的孵育细胞的时间:Tuft1和MyD88和48小时后,也可以观察到SLC30A5。探讨:簇绒1,MTMR11和SLC30A5表示表达的最高差异。在Tuft1和HSA-miR-3188(Fc + 2.48),MTMR11和Hase-miR-16(Fc-1.74)之间以及SLC30A5和HSA-MIR-30D(FC-2.01)之间确定最高影响概率。结论:蝾螈诱导参与参与耐药性的mRNA和miRNA活性的变化;然而,观察到的性格变化是抗癌治疗的预期结果。

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