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MicroRNA-320 family is downregulated in colorectal adenoma and affects tumor proliferation by targeting CDK6

机译:MicroRNA-320家族在结直肠腺瘤中下调并通过靶向CDK6影响肿瘤增殖

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摘要

AIM: To investigate the microRNA (miRNA) expression during histological progression from colorectal normal mucosa through adenoma to carcinoma within a lesion.METHODS: Using microarray, the sequential changes in miRNA expression profiles were compared in colonic lesions from matched samples; histologically, non-neoplastic mucosa, adenoma, and submucosal invasive carcinoma were microdissected from a tissue sample. Cell proliferation assay was performed to observe the effect of miRNA, and its target genes were predicted using bioinformatics approaches and the expression profile of SW480 transfected with the miRNA mimics. mRNA and protein levels of the target gene in colon cancer cell lines with a mimic control or miRNA mimics were measured using qRT-PCR and Western blotting. The expression levels of miRNA and target gene in colorectal tissue samples were also measured.RESULTS: Microarray analysis identified that the miR-320 family, including miR-320a, miR-320b, miR-320c, miR-320d and miR-320e, were differentially expressed in adenoma and submucosal invasive carcinoma. The miR-320 family, which inhibits cell proliferation, is frequently downregulated in colorectal adenoma and submucosal invasive carcinoma tissues. Seven genes including CDK6 were identified to be common in the results of gene expression array and bioinformatics analyses performed to find the target gene of the miR-320 family. We confirmed that mRNA and protein levels of CDK6 were significantly suppressed in colon cancer cell lines with miR-320 family mimics. CDK6 expression was found to increase from non-neoplastic mucosa through adenoma to submucosal invasive carcinoma tissues and showed an inverse correlation with miR-320 family expression.CONCLUSION: MiR-320 family affects colorectal tumor proliferation by targeting CDK6, plays important role in its growth, and is considered to be a biomarker for its early detection.
机译:目的:研究从大肠正常黏膜到腺瘤再到病变内癌的组织学发展过程中的微小RNA(miRNA)表达。方法:使用微阵列技术,比较匹配样品在结肠病变中miRNA表达谱的顺序变化;在组织学上,从组织样品中显微切割非肿瘤性粘膜,腺瘤和粘膜下浸润癌。进行细胞增殖测定以观察miRNA的作用,并使用生物信息学方法预测了其靶基因,并用miRNA模拟物转染了SW480的表达谱。使用qRT-PCR和Western印迹法检测具有模拟对照或miRNA模拟物的结肠癌细胞系中靶基因的mRNA和蛋白质水平。结果:通过微阵列分析发现miR-320家族包括miR-320a,miR-320b,miR-320c,miR-320d和miR-320e。在腺瘤和粘膜下浸润癌中差异表达。抑制细胞增殖的miR-320家族在大肠腺瘤和粘膜下浸润性癌组织中经常被下调。在基因表达阵列和进行生物信息学分析以发现miR-320家族目标基因的结果中,发现包括CDK6在内的七个基因是共同的。我们证实,miR-320家族模拟物在结肠癌细胞系中CDK6的mRNA和蛋白水平受到显着抑制。结论:MiR-320家族通过靶向CDK6影响结直肠肿瘤的增殖,在其生长中起重要作用。CDK6的表达从非肿瘤性粘膜到腺瘤再到粘膜下浸润性癌组织,呈负相关。 ,被认为是早期发现的生物标记。

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