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CmirC: an integrated database of clustered miRNAs co-localized with copy number variations in cancer
Akshay Pramod Ware1, Kapaettu Satyamoorthy2, Bobby Paul3
1Department of Bioinformatics, Manipal School of Life Sciences, Manipal Academy of Higher Education, Manipal, 576104, Karnataka, India.
Abstract:
Genomic rearrangements and copy number variations (CNVs) are the major regulators of clustered microRNAs (miRNAs) expression. Several clustered miRNAs are harbored in and around chromosome fragile sites (CFSs) and cancer-associated genomic hotspots. Aberrant expression of such clusters can lead to oncogenic or tumor suppressor activities. Here, we developed CmirC (Clustered miRNAs co-localized with CNVs), a comprehensive database of clustered miRNAs co-localized with CNV regions. The database consists of 481 clustered miRNAs co-localized with CNVs and their expression patterns in 35 cancer types of the TCGA. The portal also provides information on CFSs, miRNA cluster candidates, genomic coordinates, target gene networks, and gene functionality. The web portal is integrated with advanced tools such as JBrowse, NCBI-BLAST, GeneSCF, visNetwork, and NetworkD3 to help the researchers in data analysis, visualization, and browsing. This portal provides a promising avenue for integrated data analytics and offers additional evidence for the complex regulation of clustered miRNAs in cancer. The web portal is freely accessible at http://slsdb.manipal.edu/cmirclust to explore clinically significant miRNAs.
Insights
Genomic rearrangements influence clustered microRNAs (miRNAs) expression, impacting cancer. The CmirC database links clustered miRNAs with copy number variations (CNVs), aiding cancer research.
Area of Science:
- Genomics
- Cancer Biology
- Bioinformatics
Background:
- Genomic rearrangements and copy number variations (CNVs) significantly regulate clustered microRNAs (miRNAs) expression.
- Many clustered miRNAs are located near chromosome fragile sites (CFSs) and cancer-associated genomic hotspots.
- Dysregulated expression of these miRNA clusters can contribute to oncogenesis or tumor suppression.
Purpose of the Study:
- To develop CmirC, a comprehensive database for clustered miRNAs co-localized with CNVs.
- To provide a resource for analyzing miRNA expression patterns in various cancer types.
- To facilitate research into the role of clustered miRNAs in cancer development and progression.
Main Methods:
- Compiled a database of 481 clustered miRNAs co-localized with CNVs.
- Integrated expression data from 35 cancer types from The Cancer Genome Atlas (TCGA).
- Incorporated information on CFSs, miRNA cluster candidates, genomic coordinates, and target gene networks.
- Integrated advanced bioinformatics tools including JBrowse, NCBI-BLAST, GeneSCF, visNetwork, and NetworkD3.
Main Results:
- The CmirC database contains 481 clustered miRNAs co-localized with CNVs.
- Expression patterns of these miRNAs across 35 TCGA cancer types are available.
- The portal offers data on CFSs, target gene networks, and gene functionality.
- Integrated tools facilitate data analysis, visualization, and browsing.
Conclusions:
- CmirC serves as a valuable resource for exploring the complex regulation of clustered miRNAs in cancer.
- The database provides integrated analytics for understanding clinically significant miRNAs.
- It offers further evidence for the role of CNVs in regulating clustered miRNA expression in oncogenesis.
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