Yahya Shaymaa M M, Yahya Shereen M M
Hormones Department, National Research Centre, Dokki, Giza, 12622 Egypt.
Indian J Clin Biochem. 2020 Jul;35(3):353-358. doi: 10.1007/s12291-019-00824-1. Epub 2019 Mar 11.
Hepatocellular carcinoma (HCC) is one of the foremost causes of cancer related morbidity worldwide. An increasing number of studies have confirmed that microRNAs play an important role in the development, progression and metastasis of HCC. From those important miRNAs are miR-98 and miR-214. This study were conducted to explore the effect of these two miRNAs on some apoptotic and angiogenic genes namely, BCL-2, survivin, CCND1, CDC2, P53 and P21, VEGF, Hif-1α, MMP-2, MMP-9, Ang-1, Ang-2, and FGF-1. miRNAs mimics and inhibitors transfection was used to investigate the role of both studied molecules in apoptosis and angiogenesis in HepG2 cells. QRT-PCR was used for Quantitative gene and miRNA expression analyses. The study revealed that miR-98 could serve as a pro-apoptotic factor through the upregulation of P53 gene expression levels. Besides, the anti-angiogenic effect of this miRNA was evident through the down regulation of Ang-1 and FGF-1 genes. Meanwhile, miR-214 showed a pro-apoptotic role and anti-angiogenic effects. These effects were verified through the significant down regulation of BCL-2, CDC2, VEGF, Ang-1 and MMP-2. These results introduced a possible positive role played by both miR-98 and miR-214 on some pro-apoptotic and anti-angiogenic genes.
肝细胞癌(HCC)是全球范围内癌症相关发病的主要原因之一。越来越多的研究证实,微小RNA在HCC的发生、发展和转移中发挥着重要作用。其中重要的微小RNA有miR-98和miR-214。本研究旨在探讨这两种微小RNA对一些凋亡和血管生成相关基因的影响,即BCL-2、survivin、CCND1、CDC2、P53和P21、VEGF、Hif-1α、MMP-2、MMP-9、Ang-1、Ang-2和FGF-1。使用微小RNA模拟物和抑制剂转染来研究这两种分子在HepG2细胞凋亡和血管生成中的作用。采用实时定量聚合酶链反应(QRT-PCR)进行基因和微小RNA表达的定量分析。研究表明,miR-98可通过上调P53基因表达水平发挥促凋亡因子的作用。此外,该微小RNA的抗血管生成作用通过下调Ang-1和FGF-1基因得以体现。同时,miR-214也表现出促凋亡作用和抗血管生成作用。这些作用通过BCL-2、CDC2、VEGF、Ang-1和MMP-2的显著下调得到证实。这些结果表明miR-98和miR-214在一些促凋亡和抗血管生成基因上可能发挥了积极作用。