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Updated: Oct 18, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
MicroRNAs regulating SOX2 in cancer progression and therapy response
Sepideh Mirzaei1, Hamidreza Saebfar2, Mohammad Hossein Gholami3
1Department of Biology, Faculty of Science, Islamic Azad University, Science and Research Branch, Tehran, Iran.
Abstract:
The proliferation, metastasis and therapy response of tumour cells are tightly regulated by interaction among various signalling networks. The microRNAs (miRNAs) can bind to 3'-UTR of mRNA and down-regulate expression of target gene. The miRNAs target various molecular pathways in regulating biological events such as apoptosis, differentiation, angiogenesis and migration. The aberrant expression of miRNAs occurs in cancers and they have both tumour-suppressor and tumour-promoting functions. On the contrary, SOX proteins are capable of binding to DNA and regulating gene expression. SOX2 is a well-known member of SOX family that its overexpression in different cancers to ensure progression and stemness. The present review focuses on modulatory impact of miRNAs on SOX2 in affecting growth, migration and therapy response of cancers. The lncRNAs and circRNAs can function as upstream mediators of miRNA/SOX2 axis in cancers. In addition, NF-κB, TNF-α and SOX17 are among other molecular pathways regulating miRNA/SOX2 axis in cancer. Noteworthy, anti-cancer compounds including bufalin and ovatodiolide are suggested to regulate miRNA/SOX2 axis in cancers. The translation of current findings to clinical course can pave the way to effective treatment of cancer patients and improve their prognosis.
Insights
MicroRNAs (miRNAs) regulate SOX2 expression, impacting cancer growth, migration, and therapy response. This axis involves lncRNAs, circRNAs, and signaling pathways, offering potential therapeutic targets for cancer treatment.
Area of Science:
- Molecular Biology
- Cancer Research
- Genetics
Background:
- Tumor cell proliferation, metastasis, and therapy response are controlled by complex signaling networks.
- MicroRNAs (miRNAs) are small non-coding RNAs that regulate gene expression by binding to mRNA 3'-UTRs.
- Aberrant miRNA expression is linked to various cancers, exhibiting both tumor-suppressive and tumor-promoting roles.
Purpose of the Study:
- To review the modulatory impact of miRNAs on SOX2 in cancer.
- To explore how the miRNA/SOX2 axis influences cancer growth, migration, and therapy response.
- To identify upstream mediators and regulatory pathways of the miRNA/SOX2 axis in cancer.
Main Methods:
- Literature review of studies investigating miRNA and SOX2 interactions in cancer.
- Analysis of molecular pathways, including lncRNAs, circRNAs, NF-κB, and TNF-α, that regulate the miRNA/SOX2 axis.
- Examination of the role of anti-cancer compounds in modulating the miRNA/SOX2 axis.
Main Results:
- SOX2 overexpression is associated with cancer progression and stemness.
- miRNAs modulate SOX2 activity, affecting critical cancer hallmarks like growth and migration.
- lncRNAs, circRNAs, NF-κB, TNF-α, and SOX17 are key regulators of the miRNA/SOX2 axis.
- Specific anti-cancer compounds, such as bufalin and ovatodiolide, can regulate this axis.
Conclusions:
- The miRNA/SOX2 axis is a critical regulatory network in cancer.
- Understanding this axis provides insights into cancer development and progression.
- Targeting the miRNA/SOX2 axis holds promise for novel cancer therapeutic strategies and improved patient prognosis.
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