Classical and noncanonical functions of miRNAs in cancers
Alterations in microRNAs (miRNAs) expression are causative in the initiation and progression of human cancers. The molecular events responsible for the widespread differential expression of miRNAs in malignancy are exemplified by their location in cancer-associated genomic regions, epigenetic mechan...
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Published in | Trends in genetics Vol. 38; no. 4; pp. 379 - 394 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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England
Elsevier Ltd
01.04.2022
Elsevier |
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Abstract | Alterations in microRNAs (miRNAs) expression are causative in the initiation and progression of human cancers. The molecular events responsible for the widespread differential expression of miRNAs in malignancy are exemplified by their location in cancer-associated genomic regions, epigenetic mechanisms, transcriptional dysregulation, chemical modifications and editing, and alterations in miRNA biogenesis proteins. The classical miRNA function is synonymous with post-transcriptional repression of target protein genes. However, several studies have reported miRNAs functioning outside this paradigm and some of these novel modes of regulation of gene expression have been implicated in cancers. Here, we summarize key aspects of miRNA involvement in cancer, with a special focus on these lesser-studied mechanisms of action.
Germline and somatic mutations of miRNAs, their targets, and processing proteins have major implications in cancer initiation and progression.Epigenetic regulation and modification of primary, precursor, and mature miRNAs transcripts, in addition to miRNA biogenesis proteins, are additional regulatory mechanisms for miRNA transcription, maturation, and target recognition implicated in cancer.The number and extent of noncanonical functions of miRNAs are increasing and are associated with cancer.Viral miRNAs (xeno-miRNAs) have similar sequences to human miRNAs, sharing a similar pool of targets (target mimicry) and are secreted into bodily fluids in malignant diseases, thereby having potential as novel cancer biomarkers. |
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AbstractList | Alterations in microRNAs (miRNAs) expression are causative in the initiation and progression of human cancers. The molecular events responsible for the widespread differential expression of miRNAs in malignancy are exemplified by their location in cancer-associated genomic regions, epigenetic mechanisms, transcriptional dysregulation, chemical modifications and editing, and alterations in miRNA biogenesis proteins. The classical miRNA function is synonymous with post-transcriptional repression of target protein genes. However, several studies have reported miRNAs functioning outside this paradigm and some of these novel modes of regulation of gene expression have been implicated in cancers. Here, we summarize key aspects of miRNA involvement in cancer, with a special focus on these lesser-studied mechanisms of action.
Germline and somatic mutations of miRNAs, their targets, and processing proteins have major implications in cancer initiation and progression.Epigenetic regulation and modification of primary, precursor, and mature miRNAs transcripts, in addition to miRNA biogenesis proteins, are additional regulatory mechanisms for miRNA transcription, maturation, and target recognition implicated in cancer.The number and extent of noncanonical functions of miRNAs are increasing and are associated with cancer.Viral miRNAs (xeno-miRNAs) have similar sequences to human miRNAs, sharing a similar pool of targets (target mimicry) and are secreted into bodily fluids in malignant diseases, thereby having potential as novel cancer biomarkers. Alterations in microRNAs (miRNAs) expression are causative in the initiation and progression of human cancers. The molecular events responsible for the widespread differential expression of miRNAs in malignancy are exemplified by their location in cancer-associated genomic regions, epigenetic mechanisms, transcriptional dysregulation, chemical modifications and editing, and alterations in miRNA biogenesis proteins. The classical miRNA function is synonymous with post-transcriptional repression of target protein genes. However, several studies have reported miRNAs functioning outside this paradigm and some of these novel modes of regulation of gene expression have been implicated in cancers. Here, we summarize key aspects of miRNA involvement in cancer, with a special focus on these lesser-studied mechanisms of action.Alterations in microRNAs (miRNAs) expression are causative in the initiation and progression of human cancers. The molecular events responsible for the widespread differential expression of miRNAs in malignancy are exemplified by their location in cancer-associated genomic regions, epigenetic mechanisms, transcriptional dysregulation, chemical modifications and editing, and alterations in miRNA biogenesis proteins. The classical miRNA function is synonymous with post-transcriptional repression of target protein genes. However, several studies have reported miRNAs functioning outside this paradigm and some of these novel modes of regulation of gene expression have been implicated in cancers. Here, we summarize key aspects of miRNA involvement in cancer, with a special focus on these lesser-studied mechanisms of action. Alterations in microRNAs (miRNAs) expression are causative in the initiation and progression of human cancers. The molecular events responsible for the widespread differential expression of miRNAs in malignancy are exemplified by their location in cancer-associated genomic regions, epigenetic mechanisms, transcriptional dysregulation, chemical modifications and editing, and alterations in miRNA biogenesis proteins. The classical miRNA function is synonymous with post-transcriptional repression of target protein genes. However, several studies have reported miRNAs functioning outside this paradigm and some of these novel modes of regulation of gene expression have been implicated in cancers. Here, we summarize key aspects of miRNA involvement in cancer, with a special focus on these lesser-studied mechanisms of action. |
Author | Knutsen, Erik Dragomir, Mihnea P. Calin, George A. |
Author_xml | – sequence: 1 givenname: Mihnea P. surname: Dragomir fullname: Dragomir, Mihnea P. email: mihnea.dragomir@charite.de organization: Institute of Pathology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin and Berlin Institute of Health, Berlin, Germany – sequence: 2 givenname: Erik surname: Knutsen fullname: Knutsen, Erik email: erik.knutse@uit.no organization: Department of Medical Biology, Faculty of Health Sciences, UiT-The Arctic University of Norway, Tromsø, Norway – sequence: 3 givenname: George A. surname: Calin fullname: Calin, George A. email: gcalin@mdanderson.org organization: Department of Translational Molecular Pathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/34728089$$D View this record in MEDLINE/PubMed |
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Keywords | germline and somatic mutations miRNA mimicry miRNA cancer non-canonical functions pri- and pre-miRNA regulation |
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SubjectTerms | cancer Epigenesis, Genetic - genetics Gene Expression germline and somatic mutations Humans MicroRNAs - genetics miRNA miRNA mimicry Neoplasms - genetics non-canonical functions pri- and pre-miRNA regulation |
Title | Classical and noncanonical functions of miRNAs in cancers |
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