Aberrant regulation of CXCR4 in cancer via deviant microRNA-targeted interactions

Bibliographic Details
Title: Aberrant regulation of CXCR4 in cancer via deviant microRNA-targeted interactions
Authors: Alexei J. Stuckel, Tripti Khare, Marc Bissonnette, Sharad Khare
Source: Epigenetics, Vol 17, Iss 13, Pp 2318-2331 (2022)
Publisher Information: Taylor & Francis Group, 2022.
Publication Year: 2022
Collection: LCC:Genetics
Subject Terms: microrna, oncomir, cxcr4, tumour suppressor, oncoviruses, microrna mimics, Genetics, QH426-470
More Details: CXCR4 is involved in many facets of cancer, including being a major player in establishing metastasis. This is in part due to the deregulation of CXCR4, which can be attributed to many genetic and epigenetic mechanisms, including aberrant microRNA–CXCR4 interaction. MicroRNAs (miRNAs) are a type of small non-coding RNA that primarily targets the 3’ UTR of mRNA transcripts, which in turn suppresses mRNA and subsequent protein expression. In this review, we reported and characterized the many aberrant miRNA–CXCR4 interactions that occur throughout human cancers. In particular, we reported known target sequences located on the 3’ UTR of CXCR4 transcripts that tumour suppressor miRNAs bind and therefore regulate expression by. From these aberrant interactions, we also documented affected downstream genes/pathways and whether a particular tumour suppressor miRNA was reported as a prognostic marker in its respected cancer type. In addition, a limited number of cancer-causing miRNAs coined ‘oncomirs’ were reported and described in relation to CXCR4 regulation. Moreover, the mechanisms underlying both tumour suppressor and oncomir deregulations concerning CXCR4 expression were also explored. Furthermore, the miR-146a-CXCR4 axis was delineated in oncoviral infected endothelial cells in the context of virus-causing cancers. Lastly, miRNA-driven therapies and CXCR4 antagonist drugs were discussed as potential future treatment options in reported cancers pertaining to deregulated miRNA–CXCR4 interactions.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1559-2294
1559-2308
15592294
Relation: https://doaj.org/toc/1559-2294; https://doaj.org/toc/1559-2308
DOI: 10.1080/15592294.2022.2118947
Access URL: https://doaj.org/article/ee2dbae64af94adf8ad00e06d8e14eb6
Accession Number: edsdoj.2dbae64af94adf8ad00e06d8e14eb6
Database: Directory of Open Access Journals
More Details
ISSN:15592294
15592308
DOI:10.1080/15592294.2022.2118947
Published in:Epigenetics
Language:English