Ozcan Onder, Kara Murat, Yumrutas Onder, Bozgeyik Esra, Bozgeyik Ibrahim, Celik Ozgur Ilhan
Faculty of Medicine, Department of General Surgery, Mugla Sitki Kocman University, Mugla, Turkey.
Faculty of Medicine, Department of Medical Genetics, Mugla Sitki Kocman University, Mugla, Turkey.
Tumour Biol. 2016 May;37(5):6637-45. doi: 10.1007/s13277-015-4550-4. Epub 2015 Dec 7.
Deregulated microRNA (miRNA) expression has been shown to be involved in the pathogenesis of several types of cancers including colorectal cancer (CRC). Thus, determining miRNA targets of genes that play critical role in the malignant transformation is very important. Here, expression levels of tumor suppressor microtubule-associated tumor suppressor 1 (MTUS1) and its regulatory miRNAs were reported. Predicted and validated targets of MTUS1 gene was determined by a computational approach. Expressions of MTUS1 and miRNAs were determined by using 96.96 Dynamic Array™ integrated fluidic circuit (Fluidigm). As a result, MTUS1 levels were found to be diminished in formalin-fixed, paraffin-embedded (FFPE) tissue samples of CRC patients compared to controls. Also, several of MTUS1 targeting miRNAs were found to be upregulated in CRC samples (miR-373-3p, 183-5p, 142-5p, 200c-3p, 19a-3p, -20a-5p, -181a-5p, -184, -181d-5p, -372-3p, 27b-3p, 98-5p, -let-7i-5p, -let-7d-5p, -let-7g-5p, -let-7b-5p, and -let-7c-5p). Of these miRNAs, miR-135b-5p, -373-3p, 183-5p, 142-5p, 200c-3p, 19a-3p showed marked expression levels. In contrast, expression levels of let-7a-5p, 7e-5p, 7f-5p, hsa-miR-125a-5p, and 125b-5p were found to be downregulated in CRC tissues. Accordingly, some of the overexpressed miRNAs especially the miR-135b-5p, -373-3p, 183-5p, 142-5p, 200c-3p, and 19a-3p may play key roles in CRC pathophysiology through MTUS1. In contrast, let-7a-5p, 7e-5p, 7f-5p, miR-125a-5p, and 125b-5p may play important roles in CRC carcinogenesis independent from the MTUS1. In conclusion, MTUS1 targeting miRNAs may play key roles in the development of CRC by downregulating tumor suppressor MTUS1.
失调的微小RNA(miRNA)表达已被证明与包括结直肠癌(CRC)在内的多种癌症的发病机制有关。因此,确定在恶性转化中起关键作用的基因的miRNA靶标非常重要。在此,报告了肿瘤抑制因子微管相关肿瘤抑制因子1(MTUS1)及其调控miRNA的表达水平。通过计算方法确定了MTUS1基因的预测和验证靶标。使用96.96动态阵列™集成流体电路(Fluidigm)测定MTUS1和miRNA的表达。结果发现,与对照组相比,CRC患者福尔马林固定、石蜡包埋(FFPE)组织样本中MTUS1水平降低。此外,发现几种靶向MTUS1的miRNA在CRC样本中上调(miR-373-3p、183-5p、142-5p、200c-3p、19a-3p、-20a-5p、-181a-5p、-184、-181d-5p、-372-3p、27b-3p、98-5p、-let-7i-5p、-let-7d-5p、-let-7g-5p、-let-7b-5p和-let-7c-5p)。在这些miRNA中,miR-135b-5p、-373-3p、183-5p、142-5p、200c-3p、19a-3p表现出显著的表达水平。相反,发现let-7a-5p、7e-5p、7f-5p、hsa-miR-125a-5p和125b-5p在CRC组织中的表达水平下调。因此,一些过表达的miRNA,尤其是miR-135b-5p、-373-3p、183-5p、142-5p、200c-3p和19a-3p,可能通过MTUS1在CRC病理生理学中起关键作用。相反,let-7a-5p、7e-5p、7f-5p、miR-125a-5p和125b-5p可能在独立于MTUS1的CRC致癌过程中起重要作用。总之,靶向MTUS1的miRNA可能通过下调肿瘤抑制因子MTUS1在CRC的发生发展中起关键作用。