miRNA interplay: mechanisms and consequences in cancer
- Publisher:
- Company of Biologists
- Publication Type:
- Journal Article
- Citation:
- Disease Models and Mechanisms, 2021, 14, (4), pp. 1-9
- Issue Date:
- 2021-04-01
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Full metadata record
Field | Value | Language |
---|---|---|
dc.contributor.author |
Hill, M |
|
dc.contributor.author |
Tran, N |
|
dc.date.accessioned | 2023-03-27T23:12:05Z | |
dc.date.available | 2023-03-27T23:12:05Z | |
dc.date.issued | 2021-04-01 | |
dc.identifier.citation | Disease Models and Mechanisms, 2021, 14, (4), pp. 1-9 | |
dc.identifier.issn | 1754-8403 | |
dc.identifier.issn | 1754-8411 | |
dc.identifier.uri | http://hdl.handle.net/10453/168637 | |
dc.description.abstract | Canonically, microRNAs (miRNAs) control mRNA expression. However, studies have shown that miRNAs are also capable of targeting non-coding RNAs, including long non-coding RNAs and miRNAs. The latter, termed a miRNA:miRNA interaction, is a form of self-regulation. In this Review, we discuss the three main modes of miRNA:miRNA regulation: direct, indirect and global interactions, and their implications in cancer biology. We also discuss the cell-type-specific nature of miRNA:miRNA interactions, current experimental approaches and bioinformatic techniques, and how these strategies are not sufficient for the identification of novel miRNA:miRNA interactions. The self-regulation of miRNAs and their impact on gene regulation has yet to be fully understood. Investigating this hidden world of miRNA self-regulation will assist in discovering novel regulatory mechanisms associated with disease pathways | |
dc.format | Print-Electronic | |
dc.language | eng | |
dc.publisher | Company of Biologists | |
dc.relation.ispartof | Disease Models and Mechanisms | |
dc.relation.isbasedon | 10.1242/dmm.047662 | |
dc.rights | info:eu-repo/semantics/openAccess | |
dc.subject | 06 Biological Sciences, 11 Medical and Health Sciences | |
dc.subject.classification | Developmental Biology | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | MicroRNAs | |
dc.subject.mesh | Models, Biological | |
dc.subject.mesh | Neoplasms | |
dc.subject.mesh | Transcription Factors | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Humans | |
dc.subject.mesh | Neoplasms | |
dc.subject.mesh | Transcription Factors | |
dc.subject.mesh | MicroRNAs | |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | |
dc.subject.mesh | Models, Biological | |
dc.subject.mesh | Animals | |
dc.subject.mesh | Gene Expression Regulation, Neoplastic | |
dc.subject.mesh | Humans | |
dc.subject.mesh | MicroRNAs | |
dc.subject.mesh | Models, Biological | |
dc.subject.mesh | Neoplasms | |
dc.subject.mesh | Transcription Factors | |
dc.title | miRNA interplay: mechanisms and consequences in cancer | |
dc.type | Journal Article | |
utslib.citation.volume | 14 | |
utslib.location.activity | England | |
utslib.for | 06 Biological Sciences | |
utslib.for | 11 Medical and Health Sciences | |
pubs.organisational-group | /University of Technology Sydney | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Science | |
pubs.organisational-group | /University of Technology Sydney/Strength - CHT - Health Technologies | |
pubs.organisational-group | /University of Technology Sydney/Faculty of Engineering and Information Technology/School of Biomedical Engineering | |
pubs.organisational-group | /University of Technology Sydney/Centre for Health Technologies (CHT) | |
utslib.copyright.status | open_access | * |
pubs.consider-herdc | false | |
dc.date.updated | 2023-03-27T23:12:04Z | |
pubs.issue | 4 | |
pubs.publication-status | Published | |
pubs.volume | 14 | |
utslib.citation.issue | 4 |
Abstract:
Canonically, microRNAs (miRNAs) control mRNA expression. However, studies have shown that miRNAs are also capable of targeting non-coding RNAs, including long non-coding RNAs and miRNAs. The latter, termed a miRNA:miRNA interaction, is a form of self-regulation. In this Review, we discuss the three main modes of miRNA:miRNA regulation: direct, indirect and global interactions, and their implications in cancer biology. We also discuss the cell-type-specific nature of miRNA:miRNA interactions, current experimental approaches and bioinformatic techniques, and how these strategies are not sufficient for the identification of novel miRNA:miRNA interactions. The self-regulation of miRNAs and their impact on gene regulation has yet to be fully understood. Investigating this hidden world of miRNA self-regulation will assist in discovering novel regulatory mechanisms associated with disease pathways
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