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Genomic alterations as mediators of miRNA dysregulation in ovarian cancer
Casina W S Kan1, Viive M Howell, Michael A Hahn
1Hormones and Cancer Group, Kolling Institute of Medical Research, University of Sydney, Royal North Shore Hospital, St Leonards, Sydney, NSW 2065, Australia.
Abstract:
Ovarian cancer is the fifth most common cause of cancer death in women worldwide. Serous epithelial ovarian cancer (SEOC) is the most common and aggressive histological subtype. Widespread genomic alterations go hand-in-hand with aberrant DNA damage signaling and are a hallmark of high-grade SEOC. MicroRNAs (miRNAs) are a class of small noncoding RNA molecules that are nonrandomly distributed in the genome. They are frequently located in chromosomal regions susceptible to copy number variation (CNV) associated with malignancy that can influence their expression. Widespread changes in miRNA expression have been reported in multiple cancer types including ovarian cancer. This review examines CNV and single nucleotide polymorphisms, two common types of genomic alterations that occur in ovarian cancer, in the context of their influence on the expression of miRNA and the ability of miRNA to bind to and regulate their target genes. This includes genes encoding proteins involved in DNA repair and the maintenance of genomic stability. Improved understanding of mechanisms of miRNA dysregulation and the role of miRNA in ovarian cancer will provide further insight into the pathogenesis and treatment of this disease.
Insights
Genomic alterations like copy number variations influence microRNA (miRNA) expression in ovarian cancer. Understanding these changes in miRNA is key to improving ovarian cancer treatment and understanding its development.
Area of Science:
- Genomics
- Molecular Biology
- Oncology
Background:
- Ovarian cancer is a leading cause of cancer death in women globally.
- Serous epithelial ovarian cancer (SEOC) is the most prevalent and aggressive subtype.
- Genomic alterations and aberrant DNA damage signaling are characteristic of high-grade SEOC.
Purpose of the Study:
- To review the influence of genomic alterations on microRNA (miRNA) expression in ovarian cancer.
- To explore how copy number variations (CNVs) and single nucleotide polymorphisms affect miRNA regulation.
- To understand the role of miRNA in regulating genes involved in DNA repair and genomic stability.
Main Methods:
- Literature review focusing on genomic alterations in ovarian cancer.
- Analysis of the impact of CNVs and single nucleotide polymorphisms on miRNA expression.
- Examination of miRNA's role in regulating target genes, including those in DNA repair pathways.
Main Results:
- Genomic alterations, including CNVs and single nucleotide polymorphisms, are common in ovarian cancer.
- These alterations can significantly affect miRNA expression levels.
- Dysregulated miRNAs can impact the expression of genes critical for DNA repair and genomic stability.
Conclusions:
- Understanding miRNA dysregulation mechanisms in ovarian cancer is crucial.
- Investigating the role of miRNA in ovarian cancer pathogenesis offers insights into potential therapeutic targets.
- Further research into miRNA and genomic alterations can advance ovarian cancer treatment strategies.
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