Farooqi Ammad Ahmad, Qureshi Muhammad Zahid, Attar Rukset, Alhewairini Saleh S, Fayyaz Sundas, Sabitaliyevich Uteuliyev Yerzhan, Duisenbayevich Tuyebakhov Meirzhan, Alaaeddine Nada
Institute of Biomedical and Genetic Engineering (IBGE), Islamabad, Pakistan.
Department of Chemistry, GCU, Lahore, Pakistan.
Cell Mol Biol (Noisy-le-grand). 2019 Jul 31;65(6):1-5.
Central dogma of molecular biology, a term coined by Francis Crick in 1958 was considered to be the cornerstone of molecular biology unless molecular biologists challenged the idea after ground-breaking discovery of non-coding RNAs. Discovery of microRNAs marked a new era and revolutionized our understanding related to puzzling mysteries about intermediate steps between transcription and translation. Technological advancements have spawned a multitude of platforms for profiling of long-noncoding RNAs and miRNAs in different cancers. Detailed investigation of mRNA targets of miRNAs has enabled high-order analyses of interconnected networks and revealed affected pathways in different cancers. miR-143 has emerged as a multi-talented tumor suppressor microRNA having considerable ability to inhibit and prevent cancer via regulation of myriad of oncogenes. In this review, we will summarize most recent evidence related to characteristically unique ability of miR-143 to target different oncogenic mRNAs in different cancers. We will also comprehensively discuss how scientists have identified multiple long non-coding RNAs reportedly involved in promoting the expression of oncogenes by interfering with miR-143 mediated targeting of these oncogenes. Because of excellent ability of miR-143 to effectively target oncogenic mRNAs, researchers have started to focus on use of miR-143 mimics to restore expression of miR-143 in various cancers.
分子生物学的中心法则由弗朗西斯·克里克于1958年提出,在非编码RNA被突破性发现之前,一直被视为分子生物学的基石。微小RNA的发现标志着一个新时代的到来,彻底改变了我们对转录和翻译之间中间步骤相关谜题的理解。技术进步催生了众多用于分析不同癌症中长链非编码RNA和微小RNA的平台。对微小RNA的信使核糖核酸靶标的详细研究使得对相互关联网络的高阶分析成为可能,并揭示了不同癌症中受影响的信号通路。miR-143已成为一种多才多艺的肿瘤抑制微小RNA,具有通过调控众多癌基因来抑制和预防癌症的显著能力。在这篇综述中,我们将总结与miR-143在不同癌症中靶向不同致癌信使核糖核酸的独特能力相关的最新证据。我们还将全面讨论科学家如何鉴定出多个据报道通过干扰miR-143介导的对这些癌基因的靶向作用来促进癌基因表达的长链非编码RNA。由于miR-143有效靶向致癌信使核糖核酸的出色能力,研究人员已开始关注使用miR-143模拟物来恢复miR-143在各种癌症中的表达。