Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Cairo University, Cairo, Egypt.
Medical Biochemistry Department, Faculty of Medicine, Assiut University, Assiut, Egypt.
Mol Cell Biochem. 2019 Apr;454(1-2):177-189. doi: 10.1007/s11010-018-3462-1. Epub 2018 Oct 24.
Colorectal cancer (CRC) is a major cause of death worldwide. Novel non-invasive, high diagnostic value screening test is urgently needed to improve survival rate, treatment and prognosis. Stable, small, circulating microRNA (miRNA) offers unique opportunities for the early diagnosis of several diseases. It acts as tumor oncogenes or suppressors and involve in cell death, survival, and metastasis. Communication between miRNA and carcinogenesis is critical but it still not clear and needs further investigation. The aim of our study is to evaluate the role of miR-210, miR-21, miR-126, as non-invasive diagnostic biomarkers for screening, early detection of CRC, studying their correlation with prognostic variables, and clarifying the roles of miRNAs on HIF-1α-VEGF signaling pathway. The expression of miR-210, miR-21 and miR-126 was performed using qRT-PCR in adenocarcinoma (no = 35), adenomas (no = 51), and neoplasm free controls (no = 101). Serum levels of VEGF and HIF-1α was determined by ELISA Kit. The results show that the expression of miR-210, miR-21, VEGF, HIF-1α was significantly up-regulated while that miRNA-126 was down-regulated in both adenocarcinoma and adenomas compared with controls (p < 0.001 for each). No significant difference was noted comparing patients with adenocarcinoma and adenomas. The three miRNAs correlated with VEGF, HIF-α. The miR-210 and miR-21 associated with TNM classification and clinical staging of adenocarcinoma (p < 0.001) and they show high diagnostic value with sensitivity and specificity 88.6%, 90.1% and 91.4%, 95.0% respectively. Our study revealed that circulating miR-210, miR-21 were up-regulated while miR-126 was down-regulated in CRC and adenomas patients, they all correlated with TNM staging and they had high diagnostic value. HIF-1α VEGF signaling pathways regulated by miRNAs played a role in colon cancer initiation. To the best of our knowledge, this is the first study of this miRNAs panel in CRC in our community. These data suggested that these biomarkers could be a potential novel, non-invasive marker for early diagnosis, screening and predicting prognosis of CRC. Understanding the molecular functions by which miRNAs affect cancer and understanding its roles in modulating the signaling output of VEGF might be fruitful in reducing the incidence and slowing the progression of this dark malignancy.
结直肠癌(CRC)是全球主要的死亡原因。迫切需要新型非侵入性、高诊断价值的筛查试验来提高生存率、治疗效果和预后。稳定、微小、循环的 microRNA(miRNA)为多种疾病的早期诊断提供了独特的机会。miRNA 作为肿瘤致癌基因或抑癌基因,参与细胞死亡、存活和转移。miRNA 与癌症发生之间的通讯至关重要,但仍不清楚,需要进一步研究。我们的研究目的是评估 miR-210、miR-21 和 miR-126 作为非侵入性诊断生物标志物在 CRC 的筛查、早期检测中的作用,研究它们与预后变量的相关性,并阐明 miRNA 在 HIF-1α-VEGF 信号通路中的作用。使用 qRT-PCR 检测腺癌(n=35)、腺瘤(n=51)和无肿瘤对照(n=101)中 miR-210、miR-21 和 miR-126 的表达。通过 ELISA 试剂盒测定 VEGF 和 HIF-1α 的血清水平。结果表明,与对照组相比,腺癌和腺瘤中 miR-210、miR-21、VEGF、HIF-1α 的表达均显著上调,而 miRNA-126 下调(每个均 p<0.001)。腺癌和腺瘤患者之间无显著差异。这三个 miRNA 与 VEGF、HIF-α 相关。miR-210 和 miR-21 与腺癌的 TNM 分类和临床分期相关(p<0.001),它们具有高诊断价值,灵敏度和特异性分别为 88.6%、90.1%和 91.4%、95.0%。我们的研究表明,CRC 和腺瘤患者中循环 miR-210、miR-21 上调,而 miR-126 下调,它们均与 TNM 分期相关,具有高诊断价值。miRNA 调节的 HIF-1α-VEGF 信号通路在结肠癌的发生中起作用。据我们所知,这是我们社区中首次对该 miRNA 进行 CRC 研究。这些数据表明,这些生物标志物可能是 CRC 早期诊断、筛查和预测预后的潜在新型非侵入性标志物。了解 miRNA 影响癌症的分子功能及其调节 VEGF 信号输出的作用,可能有助于降低这种恶性肿瘤的发病率并减缓其进展。