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Updated: Mar 20, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Micro RNA 34a and Let-7a Expression in Human Breast Cancers is Associated with Apoptotic Expression Genes
Behzad Mansoori1, Ali Mohammadi, Solmaz Shirjang
1Immunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran
Abstract:
Breast cancer is the most common cause of cancer-related death among women in the whole world. MiR- 34a and let-7a are well known tumor suppressors that participate in the regulation of apoptosis, invasion and other cellular functions. In this study, expression of miR-34a, let-7a and apoptosis pathway genes such as Bcl-2, Caspase-3 and P53 were evaluated using quantitative real-time PCR in 45 paired samples of normal margin and tumor tissue collected from breast cancer patient at advanced stage (3-4). MiR-34a, let-7a, caspase-3 and P53 expression are reduced and Bcl-2 expression is increased within tumoral tissues in comparison with normal margin tissues. P53 expression directly or indirectly was correlated with miR-34a, let-7a, Bcl-2 and caspase-3 expression. In This study we found that MiR-34a and let-7a expression are reduced in the tumoral tissues. Down- regulation of these two molecules correlated with expression of genes associated with apoptosis. These results suggest that due to the correlation of miR-34a and let-7a with apoptotic and anti-apoptotic pathways these molecules could participate as regulators in advanced clinical stages of breast cancer and should be considered as markers for diagnosis, prognostic assessment and targeted therapy.
Insights
MicroRNAs miR-34a and let-7a are downregulated in advanced breast cancer tissues, correlating with altered apoptosis gene expression. These findings suggest their potential as diagnostic and therapeutic markers for late-stage breast cancer.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Breast cancer is a leading cause of cancer mortality in women globally.
- MicroRNAs (miRNAs) like miR-34a and let-7a are recognized tumor suppressors involved in crucial cellular processes.
- Dysregulation of miRNAs and apoptosis pathways is implicated in cancer progression.
Purpose of the Study:
- To investigate the expression levels of miR-34a, let-7a, and key apoptosis-related genes (Bcl-2, Caspase-3, P53) in advanced breast cancer.
- To explore the correlation between these miRNAs and apoptosis pathway gene expression in tumor tissues.
- To assess the potential role of miR-34a and let-7a as biomarkers in advanced breast cancer.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) was employed to analyze gene and miRNA expression.
- Paired normal margin and tumor tissue samples from 45 advanced-stage (3-4) breast cancer patients were analyzed.
- Statistical analysis was performed to determine correlations between molecular expressions.
Main Results:
- Expression of miR-34a, let-7a, Caspase-3, and P53 was significantly reduced in tumor tissues compared to normal margin tissues.
- Expression of the anti-apoptotic gene Bcl-2 was increased in tumor tissues.
- P53 expression showed a direct or indirect correlation with the expression of miR-34a, let-7a, Bcl-2, and Caspase-3.
Conclusions:
- Downregulation of miR-34a and let-7a in advanced breast cancer tissues is associated with altered expression of apoptosis-related genes.
- These miRNAs may function as regulators in advanced breast cancer stages.
- miR-34a and let-7a hold promise as potential biomarkers for diagnosis, prognostic assessment, and targeted therapy in breast cancer.
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