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Dysregulation of Non-Coding RNAs: Roles of miRNAs and lncRNAs in the Pathogenesis of Multiple Myeloma

Ismail, Nor Hayati
Mussa, Ali
Al-Khreisat, Mutaz Jamal
Mohamed Yusoff, Shafini
Husin, Azlan
Al-Jamal, Hamid Ali Nagi
Johan, Muhammad Farid
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Abstract
The dysregulation of non-coding RNAs (ncRNAs), specifically microRNAs (miRNAs) and long non-coding RNAs (lncRNAs), leads to the development and advancement of multiple myeloma (MM). miRNAs, in particular, are paramount in post-transcriptional gene regulation, promoting mRNA degradation and translational inhibition. As a result, miRNAs can serve as oncogenes or tumor suppressors depending on the target genes. In MM, miRNA disruption could result in abnormal gene expression responsible for cell growth, apoptosis, and other biological processes pertinent to cancer development. The dysregulated miRNAs inhibit the activity of tumor suppressor genes, contributing to disease progression. Nonetheless, several miRNAs are downregulated in MM and have been identified as gene regulators implicated in extracellular matrix remodeling and cell adhesion. miRNA depletion potentially facilitates the tumor advancement and resistance of therapeutic drugs. Additionally, lncRNAs are key regulators of numerous cellular processes, such as gene expression, chromatin remodeling, protein trafficking, and recently linked MM development. The lncRNAs are uniquely expressed and influence gene expression that supports MM growth, in addition to facilitating cellular proliferation and viability via multiple molecular pathways. miRNA and lncRNA alterations potentially result in anomalous gene expression and interfere with the regular functioning of MM. Thus, this review aims to highlight the dysregulation of these ncRNAs, which engender novel therapeutic modalities for the treatment of MM.
Citation
Ismail, N.H.; Mussa, A.; Al-Khreisat, M.J.; Mohamed Yusoff, S. et al 2023. "Dysregulation of Non-Coding RNAs: Roles of miRNAs and lncRNAs in the Pathogenesis of Multiple Myeloma", Non-Coding RNA, 9 (6) Article No. 68. https://doi.org/10.3390/ncrna9060068
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PubMed ID
37987364 (pubmed)
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Journal article
Language
en
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© 2024 The Authors. Published by MDPI. This is an open access article available under a Creative Commons licence. The published version can be accessed at the following link on the publisher’s website: https://doi.org/10.3390/ncrna9060068
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ISSN
2311-553X
EISSN
2311-553X
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This work was supported by the GIPS-PhD (311/PPSP/4404822) research grant from Universiti Sains Malaysia awarded to M.F.J. and N.H.I.
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Licence for published version: Creative Commons Attribution 4.0 International
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