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Identification and Validation of New Cancer Stem Cell-Related Genes and Their Regulatory microRNAs in Colorectal Cancerogenesis

机译:新癌症干细胞相关基因及其在结肠直肠癌中的调节微稻草的鉴定与验证

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摘要

Significant progress has been made in the last decade in our understanding of the pathogenetic mechanisms of colorectal cancer (CRC). Cancer stem cells (CSC) have gained much attention and are now believed to play a crucial role in the pathogenesis of various cancers, including CRC. In the current study, we validated gene expression of four genes related to CSC, L1TD1, SLITRK6, ST6GALNAC1 and TCEA3, identified in a previous bioinformatics analysis. Using bioinformatics, potential miRNA-target gene correlations were prioritized. In total, 70 formalin-fixed paraffin-embedded biopsy samples from 47 patients with adenoma, adenoma with early carcinoma and CRC without and with lymph node metastases were included. The expression of selected genes and microRNAs (miRNAs) was evaluated using quantitative PCR. Differential expression of all investigated genes and four of six prioritized miRNAs (hsa-miR-199a-3p, hsa-miR-335-5p, hsa-miR-425-5p, hsa-miR-1225-3p, hsa-miR-1233-3p and hsa-miR-1303) was found in at least one group of CRC cancerogenesis. L1TD1, SLITRK6, miR-1233-3p and miR-1225-3p were correlated to the level of malignancy. A negative correlation between miR-199a-3p and its predicted target SLITRK6 was observed, showing potential for further experimental validation in CRC. Our results provide further evidence that CSC-related genes and their regulatory miRNAs are involved in CRC development and progression and suggest that some them, particularly miR-199a-3p and its SLITRK6 target gene, are promising for further validation in CRC.
机译:在我们对结直肠癌(CRC)的致病机制的理解中,在过去十年中取得了重大进展。癌症干细胞(CSC)效应了很多关注,现在被认为在包括CRC的各种癌症的发病机制中发挥至关重要的作用。在目前的研究中,我们在先前的生物信息学分析中鉴定了与CSC,L1TD1,SLITRK6,ST6GalNAC1和TCEA3相关的四种基因的基因表达。使用生物信息学,优先考虑潜在的miRNA-靶基因相关性。共有70例福尔马林固定的石蜡嵌入活检样本,来自47例腺瘤,具有早期癌和CRC的腺瘤的腺瘤,没有淋巴结转移。使用定量PCR评价所选基因和微小RORNA(miRNA)的表达。所有研究基因的差异表达和六种优先次级的四种优先次级的含量(HSA-miR-19a-3p,Hsa-miR-335-5p,Hsa-miR-425-5p,Hsa-miR-1225-3p,Hsa-miR-1233在至少一组CRC癌症中发现-3P和HSA-MIR-1303。 L1TD1,SLITRK6,MIR-1233-3P和MIR-1225-3P与恶性肿瘤水平相关。观察到MiR-199A-3P与其预测的目标SLITRK6之间的负相关,显示CRC中进一步实验验证的潜力。我们的结果提供了进一步的证据表明CSC相关基因及其监管MiRNA参与CRC开发和进展,并建议其中一些,特别是MiR-19a-3P及其Slitrk6靶基因,是在CRC进一步验证。

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