Related Experiment Video
Updated: Mar 20, 2026

Genome-wide Screen for miRNA Targets Using the MISSION Target ID Library
Published on: April 6, 2012
Tumor suppressor microRNAs: Targeted molecules and signaling pathways in breast cancer
F Asghari1, N Haghnavaz1, B Baradaran1
1Immunology Research Center, Tabriz University of Medical Science, Tabriz, Iran; Department of Immunology, Faculty of Medicine, Tabriz University of Medical Science, Tabriz, Iran.
Abstract:
Breast cancer is the most common type of cancer in women whose prevalence is increasing every year. Common strategies for diagnosis, prognosis and specific treatment of breast cancer need improvements to increase patients' survival. For this reason, there is growing number of efforts world-wide with molecular approaches. With the advent of microRNAs (miRNAs), they have been interested for almost all aspects of tumorgenesis and correlation of breast cancer and microRNAs was discovered for the first time in 2005. MiRNAs form a group of small noncoding RNAs which participate in regulation of gene expression and subsequently several biological processes and pathogenesis of various diseases. As other cancers, miRNAs involved in breast cancer are classified in two groups: the first group is tumor inducing miRNAs (also called oncomirs) that can induce tumor initiation and progression, and their expression is increased in cancerous cells. The second group is tumor suppressor miRNAs. In normal situation, tumor suppressor miRNAs prevent beginning and progression of breast cancer through suppressing the expression of various oncogenes. In this review we will give a general overview about miRNAs and breast cancer, and in the following, more discussion about tumor suppressor miRNAs, with focus on the best known of them and their targeted oncogenes and signaling pathways. Finally, we will point to application of this group of miRNAs in diagnosis, prognosis and treatment of patients.
Insights
MicroRNAs (miRNAs) are crucial in breast cancer development. This review focuses on tumor suppressor miRNAs, exploring their role in diagnosis, prognosis, and treatment to improve patient survival.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Breast cancer incidence is rising globally, necessitating improved diagnostic and therapeutic strategies.
- MicroRNAs (miRNAs), small noncoding RNAs regulating gene expression, have emerged as key players in tumorigenesis.
- The relationship between miRNAs and breast cancer was first identified in 2005.
Purpose of the Study:
- To provide an overview of miRNAs in breast cancer.
- To focus on tumor suppressor miRNAs, their targeted oncogenes, and signaling pathways.
- To discuss the potential applications of tumor suppressor miRNAs in clinical settings.
Main Methods:
- Literature review of scientific articles on miRNAs and breast cancer.
- Analysis of the classification and function of miRNAs in breast cancer.
- Examination of the role of tumor suppressor miRNAs in oncogene regulation.
Main Results:
- MiRNAs are categorized into oncomiRs (promoting cancer) and tumor suppressor miRNAs (inhibiting cancer).
- Tumor suppressor miRNAs prevent breast cancer initiation and progression by downregulating oncogenes.
- Specific tumor suppressor miRNAs, their targeted oncogenes, and affected signaling pathways are detailed.
Conclusions:
- Tumor suppressor miRNAs hold significant potential for breast cancer diagnosis and prognosis.
- Targeting tumor suppressor miRNAs may offer novel therapeutic strategies for breast cancer patients.
- Further research into miRNA mechanisms can enhance breast cancer management and patient outcomes.
Related Concept Videos
MicroRNAs
MicroRNAs
MicroRNAs
Loss of Tumor Suppressor Gene Functions
When the tumor suppressor genes develop mutations or are lost, cells start growing out of control, leading to cancer. However, a single functional copy of the tumor suppressor gene is enough for the cells to maintain their normal functions and cell...
Loss of Tumor Suppressor Gene Functions
mTOR Signaling and Cancer Progression
The mTOR pathway or the...

