LINC00654-SOX5 mRNA-miRNA-133a 组成了新的结直肠癌 (CRC) RNA 组:一种潜在的 CRC 诊断试剂盒

IF 0.6 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Shady Montaser Mohamed, Hadeel Medhat, Sarah Keshk, Marwa Matboli, Mohamed Kamel Hassan
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引用次数: 0

摘要

摘要 利用核糖核酸(RNA)可以准确诊断许多疾病。本研究使用了一个在硅学中生成的结直肠癌(CRC)特异性 RNA 小组。这组RNA由核小体组装LINC00654(长基因间非蛋白编码RNA 654)长核小体RNA、SRY-box转录因子5(sox5 mRNA)mRNA、小核小体RNA宿主基因(Sox5)和基于硅学数据分析的遗传和表观遗传数据库中的同种microRNA-133a(miR-133a)组成。通过对 130 个病例的血清样本进行 qPCR 分析,验证并鉴定了所提出的 RNA 网络。这些病例包括 70 名恶性肿瘤 CRC 患者、40 名良性肿瘤患者和 20 名健康对照者。此外,我们还在具有代表性的 CRC 细胞系 HT29 中验证了面板的表达。我们的数据显示,与对照组相比,LINC00654 和 Sox5 RNA 在癌症患者血清中的表达量更高,而 miR-133a 则显示出相反的表达模式。这些数据至少在一定程度上验证了实验室中的关系,并提高了 miR-133a 被 LINC00654 吸收的可能性,从而为 Sox5 在 CRC 患者中的上调留下了机会。综上所述,我们的发现可能会引入一个新的分子网络。因此,该 RNA 面板可被推荐为 CRC 患者的潜在诊断标志物。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

LINC00654–SOX5 mRNA-miRNA-133a Compose New RNA Panel for Colorectal Cancer (CRC): A Potential Diagnostic Panel for CRC

LINC00654–SOX5 mRNA-miRNA-133a Compose New RNA Panel for Colorectal Cancer (CRC): A Potential Diagnostic Panel for CRC

LINC00654–SOX5 mRNA-miRNA-133a Compose New RNA Panel for Colorectal Cancer (CRC): A Potential Diagnostic Panel for CRC

Many disorders can be accurately diagnosed using ribonucleic acids (RNAs). A panel of RNAs specific to colorectal cancer (CRC), generated in silico, was used in this study. This panel is composed of Nucleosome Assembly LINC00654 (Long Intergenic Non-Protein Coding RNA 654) long nucleolar RNA, SRY-box transcription factor 5 (sox5 mRNA) mRNA, small nucleolar RNA host gene (Sox5), and homo sapiens microRNA-133a (miR-133a) from the genetic and epigenetic database based on in silico data analysis. Validation and characterization of the proposed RNA network were done by qPCR in sera samples from 130 cases. These cases included 70 CRC patients with a malignant tumour, 40 patients with a benign tumour, and 20 healthy controls. Moreover, the panel expression was verified in a representative CRC, HT29, cell line. Our data revealed that the expression of LINC00654 and Sox5 RNAs was higher in the sera from CRC compared with the control group, while miR-133a showed the opposite expression pattern. These data may, at least in part, validate the in-silico relationship and enhance the possibility that miR-133a might be sponged by LINC00654 and thus leave the chance for Sox5 upregulation in CRC patients. Taken together, our findings may introduce a novel molecular network. Therefore, this RNA panel could be recommended as a potential diagnostic marker for CRC patients.

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来源期刊
CiteScore
1.10
自引率
0.00%
发文量
31
期刊介绍: Biochemistry (Moscow), Supplement Series B: Biomedical Chemistry   covers all major aspects of biomedical chemistry and related areas, including proteomics and molecular biology of (patho)physiological processes, biochemistry, neurochemistry, immunochemistry and clinical chemistry, bioinformatics, gene therapy, drug design and delivery, biochemical pharmacology, introduction and advertisement of new (biochemical) methods into experimental and clinical medicine. The journal also publishes review articles. All issues of the journal usually contain solicited reviews.
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