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Investigating the Relation between miR-31 and RhoA Expressions in Breast Cancer Clinical Samples and Cell Lines: A Controversial Matter

机译:调查乳腺癌临床样品和细胞系中miR-31和RhoA表达之间的关系:一个有争议的问题

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Breast cancer is the most prevalent diagnosed cancer and the second cause of cancer death among women worldwide. There are different mechanisms that play crucial roles in the onset and progression of breast cancer including microRNAs. microRNAs are small noncoding RNAs that regulate gene expression by repressing translation post-transcriptionally. miR-31 is an integrin modulator implicated in different cellular processes such as apoptosis, cell cycle control, and DNA repair. According to the literature, RhoA is one of the genes regulated by miR-31. It has an important role in actin-myosin contraction and subsequently in cell motility and migration in metastasis cascade. Breast cancer cell lines, MCF-7 and MDA-MB-231, as well as normal breast cells, MCF-10A, were cultured. RNA extraction, cDNA synthesis, and SYBR Green I quantitative real-time PCR were used to investigate the expression of miR-31 and RhoA . In addition, 10 metastatic breast cancer clinical samples were analyzed to assess miR-31 and RhoA expression, and normal cells from the same patients were used as controls. Pearson’s correlation co-efficient was applied to find out any probable relation between miR-31 and RhoA expression. Gene expression analyses in MCF-7 cell line showed downregulation of miR-31 while RhoA was upregulated in the cell line (inverse correlation). miR-31 and RhoA were both upregulated in metastatic MDA-MB-231 cell line and downregulated in 90% of clinical samples. Pearson’s correlation co-efficient showed complete positive correlation between miR-31 and RhoA expression. The expression of miR-31 and RhoA is positively correlated, and it is declined in metastatic breast that cancer clinical samples save MDA-MB-231 cells. Unlike previous reports, we found that miR-31 is not the main silencer of RhoA expression. Therefore, more investigation on genes and miRNAs affecting metastasis process can elucidate new biomarkers and therapeutic targets for metastatic breast cancer. Highlights miR-31 is an important miRNA implicated in different cellular processes as well as cancer. The protein product of RhoA gene plays a role in actin-myosin contraction and cell motility in cancer metastasis. We approved bioinformatically and experimentally that RhoA is one of the genes regulated by miR-31.
机译:乳腺癌是全世界女性中最普遍诊断的癌症,也是癌症死亡的第二大原因。有多种机制在乳腺癌的发生和发展中起着至关重要的作用,包括microRNA。 microRNA是小的非编码RNA,可通过转录后抑制翻译来调节基因表达。 miR-31是一种整合素调节剂,与细胞凋亡,细胞周期控制和DNA修复等不同的细胞过程有关。根据文献,RhoA是由miR-31调控的基因之一。它在肌动蛋白-肌球蛋白的收缩以及随后在转移级联中的细胞运动和迁移中具有重要作用。培养乳腺癌细胞系MCF-7和MDA-MB-231以及正常乳腺癌细胞MCF-10A。 RNA提取,cDNA合成和SYBR Green I定量实时PCR用于研究miR-31和RhoA的表达。另外,分析了10个转移性乳腺癌临床样品以评估miR-31和RhoA表达,并将来自相同患者的正常细胞用作对照。使用Pearson的相关系数来找出miR-31与RhoA表达之间的任何可能关系。 MCF-7细胞系中的基因表达分析显示miR-31的下调而RhoA在细胞系中的上调(逆相关)。在转移的MDA-MB-231细胞系中,miR-31和RhoA均被上调,而在90%的临床样品中均被下调。皮尔逊的相关系数显示miR-31与RhoA表达完全呈正相关。 miR-31和RhoA的表达呈正相关,在转移性乳腺癌中,癌症临床样品保存MDA-MB-231细胞的表达下降。与以前的报道不同,我们发现miR-31不是RhoA表达的主要沉默子。因此,对影响转移过程的基因和miRNA的更多研究可以阐明转移性乳腺癌的新生物标志物和治疗靶标。亮点miR-31是一种重要的miRNA,与不同的细胞过程以及癌症有关。 RhoA基因的蛋白质产物在癌症转移中的肌动蛋白-肌球蛋白收缩和细胞运动中起作用。我们通过生物信息学和实验证明,RhoA是miR-31调控的基因之一。

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