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Performing Data Mining And Integrative Analysis Of Biomarker in Breast Cancer Using Multiple Publicly Accessible Databases
Published on: May 17, 2019
Data mining of micrornas in breast carcinogenesis which may be a potential target for cancer prevention
Jin-Wook Kang1,2, Min-Ji Kim1,2, Hyun-Ah Baek3
11Molecular Mechanisms of Functional Foods Laboratory, Jeonju University, Jeonju, Jeonbuk, 55069 Korea.
Abstract:
The microRNAs (miRNAs) negatively regulate the stability and translation of target messenger RNAs by selectively binding. It has been implicated in diverse processes such as cellular differentiation, cell-cycle control, apoptosis, and carcinogenesis. Examination of tumor-specific miRNA expression profiles has revealed wide spread dysregulation of these molecules in diverse cancers. The available genomic bulk evidences were extracted from The Cancer Genome Atlas by using IluminaGA_miRNASeq platform in human breast cancer samples. After mining collected data, group of each miRNA ID was analyzed through five D/Bs (mirWalk, miranda, mirDB, RNA22, and TargetScan) on predicted and validated miRNA targets. Oncogenes known to have a high correlation with breast cancer (C-myc, HER2, cyclin D-1, N-RAS, FGF-4, FGF-3, BRCA1, and BRCA2) are subject in this study to select their relevant miRNAs. Function of miRNA regulation will be essential to achieve a complete understanding of carcinogenesis and these miRNAs would be potential target for breast cancer prevention.
Insights
MicroRNAs (miRNAs) are key regulators in breast cancer development. This study identifies specific miRNAs targeting oncogenes, offering potential for novel breast cancer prevention strategies.
Area of Science:
- Molecular Biology
- Genomics
- Oncology
Background:
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression post-transcriptionally.
- Dysregulation of miRNAs is a hallmark of various cancers, including breast cancer.
- miRNAs play critical roles in cellular processes like differentiation, cell-cycle control, and apoptosis.
Purpose of the Study:
- To investigate the dysregulation of specific miRNAs in human breast cancer.
- To identify miRNAs that target key breast cancer oncogenes.
- To explore the potential of these miRNAs as targets for breast cancer prevention.
Main Methods:
- Genomic data from The Cancer Genome Atlas (TCGA) for human breast cancer samples were analyzed.
- IluminaGA_miRNASeq platform was utilized for miRNA expression profiling.
- Multiple databases (mirWalk, miranda, mirDB, RNA22, TargetScan) were employed to predict and validate miRNA targets.
- Focus was placed on miRNAs associated with known breast cancer oncogenes (e.g., C-myc, HER2, BRCA1/2).
Main Results:
- Significant dysregulation of specific miRNAs was observed in breast cancer samples.
- Several miRNAs were identified as potential regulators of key breast cancer oncogenes.
- The study provides a list of relevant miRNAs targeting oncogenes like C-myc, HER2, cyclin D-1, N-RAS, FGF-4, FGF-3, BRCA1, and BRCA2.
Conclusions:
- miRNA expression profiles are significantly altered in breast cancer.
- Targeting specific oncogene-regulating miRNAs presents a promising avenue for breast cancer prevention.
- Understanding miRNA functions in carcinogenesis is crucial for developing effective therapeutic strategies.
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