Department of Experimental Biology, University of Jaen, 23071 Jaen, Spain.
Department of Human Anatomy and Embryology, University of Extremadura, 06006 Badajoz, Spain.
Int J Mol Sci. 2022 Jan 11;23(2):764. doi: 10.3390/ijms23020764.
Deep whole genome and transcriptome sequencing have highlighted the importance of an emerging class of non-coding RNA longer than 200 nucleotides (i.e., long non-coding RNAs (lncRNAs)) that are involved in multiple cellular processes such as cell differentiation, embryonic development, and tissue homeostasis. Cancer is a prime example derived from a loss of homeostasis, primarily caused by genetic alterations both in the genomic and epigenetic landscape, which results in deregulation of the gene networks. Deregulation of the expression of many lncRNAs in samples, tissues or patients has been pointed out as a molecular regulator in carcinogenesis, with them acting as oncogenes or tumor suppressor genes. Herein, we summarize the distinct molecular regulatory mechanisms described in literature in which lncRNAs modulate carcinogenesis, emphasizing epigenetic and genetic alterations in particular. Furthermore, we also reviewed the current strategies used to block lncRNA oncogenic functions and their usefulness as potential therapeutic targets in several carcinomas.
深度全基因组和转录组测序强调了一类新兴的非编码 RNA 的重要性,这些 RNA 长度超过 200 个核苷酸(即长非编码 RNA(lncRNA)),它们参与多种细胞过程,如细胞分化、胚胎发育和组织稳态。癌症就是一个很好的例子,它源于稳态的丧失,主要是由于基因组和表观遗传景观中的遗传改变,导致基因网络的失调。在样本、组织或患者中,许多 lncRNA 的表达失调被指出是致癌作用中的分子调节剂,它们作为癌基因或肿瘤抑制基因发挥作用。本文总结了文献中描述的 lncRNA 调节致癌作用的不同分子调控机制,特别强调了表观遗传和遗传改变。此外,我们还回顾了目前用于阻断 lncRNA 致癌功能的策略及其作为几种癌的潜在治疗靶点的有用性。