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Updated: Jan 4, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
The Role and Function of microRNA in the Pathogenesis of Multiple Myeloma
Hiroshi Handa1, Yuki Murakami2, Rei Ishihara2
1Department of Hematology, Gunma University Graduate School of Medicine, 3-39-22 Showa-machi, Maebashi, Gunma 371-8511, Japan.
Abstract:
Recently, attention has been drawn to the role of non-coding regions of the genome in cancer pathogenesis. MicroRNAs (miRNAs) are small non-coding RNAs with 19-25 bases of length that control gene expression by destroying messenger RNA or inhibiting its translation. In multiple myeloma (MM), the expression of several miRNAs, such as miR-15a and miR-16, is markedly decreased and their target genes upregulated, suggesting their role as tumor-suppressing miRNAs. In contrast, miRNAs such as miR-21 and miR-221 are highly expressed and function as oncogenes (oncomiRs). In addition, several miRNAs, such as those belonging to the miR-34 family, are transcriptional targets of p53 and mediate its tumor-suppressive functions. Many miRNAs are associated with drug resistance, and the modulation of their expression or activity might be explored to reverse it. Moreover, miRNA expression patterns in either MM cells or serum exosomes have been shown to be good prognostic markers. miRNA regulation mechanisms have not been fully elucidated. Many miRNAs are epigenetically controlled by DNA methylation and histone modification, and others regulate the expression of epigenetic modifiers, indicating that miRNA and other epigenetic effectors are part of a network. In this review, we outlined the roles of miRNAs in MM and their potential to predict MM prognosis and develop novel therapies.
Insights
MicroRNAs (miRNAs) play crucial roles in multiple myeloma (MM) by acting as tumor suppressors or oncogenes. Understanding miRNA functions offers potential for novel MM therapies and prognostic markers.
Area of Science:
- Genomics
- Molecular Biology
- Oncology
Background:
- Non-coding genomic regions, particularly microRNAs (miRNAs), are increasingly recognized for their role in cancer.
- In multiple myeloma (MM), specific miRNAs are downregulated (e.g., miR-15a, miR-16) acting as tumor suppressors, while others are upregulated (e.g., miR-21, miR-221) acting as oncogenes.
- miRNAs are involved in drug resistance and can serve as prognostic markers in MM.
Purpose of the Study:
- To review the multifaceted roles of microRNAs (miRNAs) in multiple myeloma (MM).
- To explore the potential of miRNAs as prognostic biomarkers in MM.
- To discuss the therapeutic implications of targeting miRNAs in MM.
Main Methods:
- Literature review focusing on microRNA (miRNA) research in multiple myeloma (MM).
- Analysis of miRNA expression patterns and their correlation with disease progression and drug resistance.
- Examination of epigenetic regulation of miRNAs and their interaction with epigenetic modifiers.
Main Results:
- Downregulation of tumor-suppressive miRNAs (e.g., miR-15a, miR-16) and upregulation of oncogenic miRNAs (oncomiRs) are observed in MM.
- miRNAs, including the miR-34 family, are linked to p53-mediated tumor suppression.
- miRNA expression profiles in MM cells and serum exosomes show promise as prognostic indicators.
Conclusions:
- MicroRNAs (miRNAs) are integral to multiple myeloma (MM) pathogenesis, influencing tumor suppression, oncogenesis, and drug resistance.
- miRNA expression patterns hold significant potential for predicting MM prognosis.
- Modulating miRNA activity presents a promising avenue for developing novel therapeutic strategies in MM.
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