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Updated: Jun 20, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Causes and consequences of microRNA dysregulation in cancer
1Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University Medical Center, 410 West 10th Avenue, Columbus, OH 43210, USA. carlo.croce@osumc.edu
Abstract:
Over the past several years it has become clear that alterations in the expression of microRNA (miRNA) genes contribute to the pathogenesis of most--if not all--human malignancies. These alterations can be caused by various mechanisms, including deletions, amplifications or mutations involving miRNA loci, epigenetic silencing or the dysregulation of transcription factors that target specific miRNAs. Because malignant cells show dependence on the dysregulated expression of miRNA genes, which in turn control or are controlled by the dysregulation of multiple protein-coding oncogenes or tumour suppressor genes, these small RNAs provide important opportunities for the development of future miRNA-based therapies.
Insights
Altered microRNA (miRNA) gene expression is key in human cancer development. Understanding these changes offers new avenues for developing effective miRNA-based cancer therapies.
Area of Science:
- Molecular Biology
- Genetics
- Oncology
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression.
- Aberrant miRNA expression is increasingly recognized as a significant factor in human cancer development.
Purpose of the Study:
- To elucidate the role of altered miRNA gene expression in the pathogenesis of human malignancies.
- To explore the potential of miRNAs as therapeutic targets in cancer treatment.
Main Methods:
- Review of current literature on miRNA gene alterations in cancer.
- Analysis of mechanisms leading to miRNA dysregulation, including genetic and epigenetic factors.
- Examination of the interplay between miRNAs and oncogenes/tumor suppressor genes.
Main Results:
- Alterations in miRNA gene expression are implicated in the majority of human cancers.
- Mechanisms of miRNA dysregulation include genetic mutations, copy number variations, and epigenetic modifications.
- miRNAs are integral to the regulatory networks of protein-coding oncogenes and tumor suppressor genes.
Conclusions:
- Dysregulated miRNA expression is a hallmark of cancer, driving its pathogenesis.
- Targeting these dysregulated miRNAs presents a promising strategy for novel cancer therapies.
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