Derderian Camille, Orunmuyi Akintunde T, Olapade-Olaopa E Oluwabunmi, Ogunwobi Olorunseun O
Department of Biological Sciences, Hunter College of The City University of New York, New York, NY, United States.
Department of Radiation Oncology, College of Medicine, University of Ibadan, Ibadan, Nigeria.
Front Oncol. 2019 Jun 12;9:502. doi: 10.3389/fonc.2019.00502. eCollection 2019.
There is increasing evidence that PVT1 has oncogenic properties and regulates proliferation and growth of many cancers. Themolecular mechanisms of action of PVT1 are mediated, in part, by microRNAs (miRNAs). However, some well-established transcription factors involved in cancer cell proliferation share a common thread of microRNA associations with PVT1. Furthermore, these microRNAs are also involved in mechanisms that lead to the development of drug resistance in cancer cells. While several microRNAs have been implicated directly in PVT1-mediated tumorigenesis, significant steps need to be taken to elucidate these important relationships. We synthesize the current knowledge of the miRNAs and associated genes by which PVT1 contributes to tumorigenesis. Overall, the trend suggests a negative correlation of microRNA expression with PVT1. It is clear that future studies involving PVT1 should be carried out in conjunction with microRNA analysis and should include large scale lncRNA-miRNA-mRNA network analysis. Likewise, the relationship between established transcription factors such as and , and processes like epithelial-mesenchymal transition may offer valuable insight into the yet unknown mechanisms of PVTI-mediated cancer progression via microRNA-dependent signaling networks.
越来越多的证据表明,PVT1具有致癌特性,并调节多种癌症的增殖和生长。PVT1的分子作用机制部分由微小RNA(miRNA)介导。然而,一些参与癌细胞增殖的成熟转录因子与PVT1有着共同的微小RNA关联线索。此外,这些微小RNA也参与导致癌细胞耐药性产生的机制。虽然已有几种微小RNA被直接认为与PVT1介导的肿瘤发生有关,但仍需采取重大步骤来阐明这些重要关系。我们综合了目前关于PVT1促成肿瘤发生的微小RNA和相关基因的知识。总体而言,趋势表明微小RNA表达与PVT1呈负相关。显然,未来涉及PVT1的研究应与微小RNA分析相结合进行,并且应包括大规模的长链非编码RNA-微小RNA-信使RNA网络分析。同样,诸如[此处原文缺失具体转录因子名称]等成熟转录因子与上皮-间质转化等过程之间的关系,可能会为通过微小RNA依赖的信号网络介导的PVT1介导的癌症进展的未知机制提供有价值的见解。