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Identification of miR-20a as A Potential Discerning Biomarker for Non-Invasive versus Invasive Retinoblastoma
Ahmad Bereimipour1,2, Saeed Karimi3, Mohammad Faranoush4
1Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Cell Journal
|May 13, 2024
Summary
This study identified specific microRNAs (miRNAs) in blood serum that can differentiate between invasive and non-invasive retinoblastoma (RB) in children. These biomarkers, including miR-20a and miR-191, may help tailor treatments and reduce chemotherapy side effects.
Area of Science:
- Oncology
- Genetics
- Biochemistry
Background:
- Intraocular retinoblastoma (RB) is a common childhood cancer.
- Current treatment involves systemic chemotherapy due to unpredictable tumor aggressiveness.
- Differentiating invasive from non-invasive tumors could personalize treatment and minimize drug toxicity.
Purpose of the Study:
- To identify diagnostic biomarkers for distinguishing invasive from non-invasive retinoblastoma (RB).
- To analyze microRNA (miRNA) profiles in the blood serum of RB patients.
Main Methods:
- Utilized three Gene Expression Omnibus (GEO) datasets for miRNA and gene expression analysis.
- Investigated relationships between RB gene expression and miRNAs.
- Validated candidate miRNAs using real-time PCR in the Y79 cell line and patient blood samples.
Main Results:
- Identified 14 highly expressed and 7 lowly expressed miRNAs.
- Found miR-181, miR-135a, miR-20a, miR-373, and miR-191 to be differentially expressed between invasive and non-invasive RB.
- Observed increased serum miR-20a and miR-191 in invasive retinoblastomas.
Conclusions:
- Bioinformatics analysis revealed key miRNAs differentiating RB tumor states.
- miR-20a, miR-191, and miR-135a show potential as biomarkers for distinguishing non-invasive from invasive retinoblastoma.
- Further research is warranted to validate these miRNA biomarkers for clinical application.

