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Updated: Dec 21, 2025

MicroRNA Amplification and Recognition through Locked-nucleic-acid In situ Hybridization as A Novel Detection and Quantification Method
Published on: October 7, 2025
How microRNAs affect the PD-L1 and its synthetic pathway in cancer
Gholamreza Rezaei Danbaran1, Saeed Aslani2, Nadia Sharafkandi3
1Student Research Committee, Shahid Sadoughi University of Medical Sciences, Yazd, Iran.
Abstract:
Programmed cell death-ligand 1 (PD-L1) is a glycoprotein that is expressed on the cell surface of both hematopoietic and nonhematopoietic cells. PD-L1 play a role in the immune tolerance and protect self-tissues from immune system attack. Dysfunction of this molecule has been highlighted in the pathogenesis of tumors, autoimmunity, and infectious disorders. MicroRNAs (miRNAs) are endogenous molecules that are classified as small non-coding RNA with approximately 20-22 nucleotides (nt) length. The function of miRNAs is based on complementary interactions with target mRNA via matching completely or incompletely. The result of this function is decay of the target mRNA or preventing mRNA translation. In the past decades, several miRNAs have been discovered which play an important role in the regulation of PD-L1 in various malignancies. In this review, we discuss the effect of miRNAs on PD-L1 expression and consider the effect of miRNAs on the synthetic pathway of PD-L1, especially during cancers.
Insights
MicroRNAs (miRNAs) regulate Programmed Cell Death-Ligand 1 (PD-L1) expression, impacting immune tolerance and disease pathogenesis. This review explores how miRNAs influence PD-L1 synthesis, particularly in cancers.
Area of Science:
- Molecular Biology
- Immunology
- Oncology
Background:
- Programmed Cell Death-Ligand 1 (PD-L1) is a cell surface glycoprotein crucial for immune tolerance, preventing self-tissue attack.
- Dysregulation of PD-L1 is implicated in tumors, autoimmune diseases, and infections.
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression by targeting messenger RNA (mRNA).
Purpose of the Study:
- To review the regulatory role of miRNAs on PD-L1 expression.
- To investigate the impact of miRNAs on PD-L1 synthesis pathways.
- To focus on the implications of miRNA-mediated PD-L1 regulation in various cancers.
Main Methods:
- Literature review of studies investigating miRNA-PD-L1 interactions.
- Analysis of mechanisms by which miRNAs affect PD-L1 mRNA and protein levels.
- Synthesis of findings related to miRNA regulation of PD-L1 in oncogenesis.
Main Results:
- Multiple miRNAs have been identified that modulate PD-L1 expression in different cancer types.
- miRNAs can inhibit PD-L1 synthesis by targeting its mRNA for degradation or translational repression.
- This regulation is a significant factor in the immune evasion strategies of cancer cells.
Conclusions:
- miRNAs represent a critical regulatory layer controlling PD-L1 expression.
- Targeting miRNA-PD-L1 interactions offers potential therapeutic strategies for cancer treatment.
- Further research into specific miRNA-PD-L1 axes is warranted for clinical applications.
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