LncRNAs: New Players in Apoptosis Control.

Q3 Biochemistry, Genetics and Molecular Biology
International Journal of Cell Biology Pub Date : 2014-01-01 Epub Date: 2014-01-30 DOI:10.1155/2014/473857
Marianna Nicoletta Rossi, Fabrizio Antonangeli
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引用次数: 115

Abstract

The discovery that the mammalian genome is largely transcribed and that almost half of the polyadenylated RNAs is composed of noncoding RNAs has attracted the attention of the scientific community. Growing amount of data suggests that long noncoding RNAs (lncRNAs) are a new class of regulators involved not only in physiological processes, such as imprinting and differentiation, but also in cancer progression and neurodegeneration. Apoptosis is a well regulated type of programmed cell death necessary for correct organ development and tissue homeostasis. Indeed, cancer cells often show an inhibition of the apoptotic pathways and it is now emerging that overexpression or downregulation of different lncRNAs in specific types of tumors sensitize cancer cells to apoptotic stimuli. In this review we summarize the latest studies on lncRNAs and apoptosis with major attention to those performed in cancer cells and in healthy cells upon differentiation. We discuss the new perspectives of using lncRNAs as targets of anticancer drugs. Finally, considering that lncRNA levels have been reported to have a correlation with specific cancer types, we argue the possibility of using lncRNAs as tumor biomarkers.

Abstract Image

LncRNAs:细胞凋亡控制的新参与者
哺乳动物基因组大部分是转录的,近一半的聚腺苷化rna是由非编码rna组成的,这一发现引起了科学界的关注。越来越多的数据表明,长链非编码rna (lncRNAs)是一类新的调控因子,不仅参与印迹和分化等生理过程,还参与癌症进展和神经退行性变。细胞凋亡是一种受良好调控的程序性细胞死亡,是器官发育和组织稳态所必需的。事实上,癌细胞经常表现出对凋亡通路的抑制,现在研究表明,在特定类型的肿瘤中,不同lncrna的过表达或下调使癌细胞对凋亡刺激敏感。本文综述了lncRNAs与细胞凋亡的最新研究进展,重点介绍了lncRNAs在癌细胞和健康细胞分化过程中的研究进展。我们讨论了利用lncrna作为抗癌药物靶点的新视角。最后,考虑到lncRNA水平已被报道与特定癌症类型相关,我们认为使用lncRNA作为肿瘤生物标志物的可能性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
International Journal of Cell Biology
International Journal of Cell Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
3.30
自引率
0.00%
发文量
4
审稿时长
20 weeks
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