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Deregulated miRNA clusters in ovarian cancer: Imperative implications in personalized medicine
Amoolya Kandettu1, Divya Adiga1, Vasudha Devi2
1Department of Cell and Molecular Biology, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, Karnataka 576104, India.
Abstract:
Ovarian cancer (OC) is one of the most common and fatal types of gynecological cancer. OC is usually detected at the advanced stages of the disease, making it highly lethal. miRNAs are single-stranded, small non-coding RNAs with an approximate size ranging around 22 nt. Interestingly, a considerable proportion of miRNAs are organized in clusters with miRNA genes placed adjacent to one another, getting transcribed together to result in miRNA clusters (MCs). MCs comprise two or more miRNAs that follow the same orientation during transcription. Abnormal expression of the miRNA cluster has been identified as one of the key drivers in OC. MC exists both as tumor-suppressive and oncogenic clusters and has a significant role in OC pathogenesis by facilitating cancer cells to acquire various hallmarks. The present review summarizes the regulation and biological function of MCs in OC. The review also highlights the utility of abnormally expressed MCs in the clinical management of OC.
Insights
miRNA clusters (MCs) drive ovarian cancer (OC) progression by promoting cancer hallmarks. Aberrant MCs are key in OC pathogenesis and offer potential for clinical management.
Area of Science:
- Gynecological Oncology
- Molecular Biology
- Cancer Genetics
Background:
- Ovarian cancer (OC) is a leading cause of cancer death, often diagnosed late.
- MicroRNAs (miRNAs) are small non-coding RNAs crucial in gene regulation.
- miRNA clusters (MCs) are transcribed as single units and play roles in various cancers.
Purpose of the Study:
- To review the regulation and biological functions of miRNA clusters in ovarian cancer.
- To highlight the clinical utility of dysregulated miRNA clusters in OC management.
Main Methods:
- Literature review focusing on miRNA clusters in ovarian cancer.
- Analysis of regulatory mechanisms and functional roles of MCs.
- Evaluation of clinical implications of MCs in OC.
Main Results:
- Abnormal expression of MCs is a key driver in OC pathogenesis.
- MCs can act as tumor suppressors or oncogenes in OC.
- Dysregulated MCs contribute to cancer cell hallmarks and disease progression.
Conclusions:
- MCs are significantly involved in the development and progression of ovarian cancer.
- Abnormally expressed MCs represent promising biomarkers and therapeutic targets for OC.
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