Epitranscriptomics: A New Layer of microRNA Regulation in Cancer.
Epitranscriptomics: A New Layer of microRNA Regulation in Cancer.
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Epitranscriptomics:癌症中microRNA调控的新层。
DOI:
10.3390/cancers13133372
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发表时间:
2021-07-05
期刊:
影响因子:
5.2
通讯作者:
Fulci V
中科院分区:
文献类型:
--
作者:
De Paolis V;Lorefice E;Orecchini E;Carissimi C;Laudadio I;Fulci V
MicroRNAs are small non-coding RNAs, acting as post-transcriptional regulators of gene expression. In the last two decades, their role in cancer as oncogenes (oncomir), as well as tumor suppressors, has been extensively demonstrated. Recently, epitranscriptomics, namely the study of RNA modifications, has emerged as a new field of great interest, being an additional layer in the regulation of gene expression. Almost all classes of eukaryotic RNAs, including miRNAs, undergo epitranscriptomic modifications. Alterations of RNA modification pathways have been described for many diseases—in particular, in the context of malignancies. Here, we reviewed the current knowledge on the potential link between epitranscriptomic modifications of miRNAs and cancer. MicroRNAs are pervasive regulators of gene expression at the post-transcriptional level in metazoan, playing key roles in several physiological and pathological processes. Accordingly, these small non-coding RNAs are also involved in cancer development and progression. Furthermore, miRNAs represent valuable diagnostic and prognostic biomarkers in malignancies. In the last twenty years, the role of RNA modifications in fine-tuning gene expressions at several levels has been unraveled. All RNA species may undergo post-transcriptional modifications, collectively referred to as epitranscriptomic modifications, which, in many instances, affect RNA molecule properties. miRNAs are not an exception, in this respect, and they have been shown to undergo several post-transcriptional modifications. In this review, we will summarize the recent findings concerning miRNA epitranscriptomic modifications, focusing on their potential role in cancer development and progression.
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影响因子:
4.5
作者:
Alexandrov, A;Martzen, MR;Phizicky, EM
通讯作者:
Phizicky, EM
影响因子:
--
作者:
Arachchilage, Gayan Mirihana;Dassanayake, Arosha C.;Basu, Soumitra
通讯作者:
Basu, Soumitra
影响因子:
64.8
作者:
Burns, CM;Chu, H;Emeson, RB
通讯作者:
Emeson, RB
影响因子:
8.8
作者:
Aguilo F;Li S;Balasubramaniyan N;Sancho A;Benko S;Zhang F;Vashisht A;Rengasamy M;Andino B;Chen CH;Zhou F;Qian C;Zhou MM;Wohlschlegel JA;Zhang W;Suchy FJ;Walsh MJ
通讯作者:
Walsh MJ
影响因子:
4.1
作者:
Carissimi, Claudia;Laudadio, Ilaria;Fulci, Valerio
通讯作者:
Fulci, Valerio