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Updated: May 17, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
Circ_0000190 inhibits the progression of triple negative breast cancer by regulating miR-301a/MEOX2 pathway
Heng Liu1, Xiunan Li1, Gangyue Wang1
1Department of Breast Surgery, Beijing Obstetrics and Gynecology Hospital, Capital Medical University; Beijing Maternal and Child Health Care Hospital Beijing, China.
Abstract:
Circular RNA (circRNA) and microRNA (miRNA) play critical roles in regulating proliferation, apoptosis, and invasion in triple-negative breast cancer (TNBC) cells. To investigate their functional significance, we employed quantitative real-time PCR (qRT-PCR) to assess the differential expression of circ_0000190, miR-301a, and mesenchyme homeobox 2 (MEOX2) between TNBC cell lines and normal breast epithelial cells. Subsequently, we established overexpression and knockdown systems for these molecules to examine their effects on TNBC cell proliferation, apoptosis, migration, invasion, and epithelial-mesenchymal transition (EMT). Additionally, we evaluated the impact of circ_0000190 overexpression on tumor growth using a mouse xenograft model, measuring tumor volume and weight. Our findings revealed that circ_0000190 and MEOX2 expression were significantly downregulated (P<0.05) in TNBC cells compared to normal breast epithelial cells, whereas miR-301a was upregulated (P<0.05). Knockdown of circ_0000190 promoted TNBC cell proliferation, migration, invasion, and EMT, while suppressing apoptosis. Mechanistically, circ_0000190 functioned as a molecular sponge for miR-301a, and its overexpression significantly inhibited miR-301a expression (P<0.001). Notably, miR-301a mimics partially reversed the suppressive effects of circ_0000190 overexpression on proliferation, migration, invasion, and EMT, as well as its pro-apoptotic effects (P<0.001). Furthermore, we identified MEOX2 as a direct target of miR-301a. MEOX2 knockdown attenuated the inhibitory effects of miR-301a silencing on proliferation, migration, invasion, and EMT, while also counteracting its pro-apoptotic function. In vivo experiments demonstrated that circ_0000190 overexpression significantly reduced tumor volume and weight (P<0.001), concomitant with elevated MEOX2 mRNA and protein levels (P<0.001) and decreased miR-301a expression (P<0.001). In conclusion, our study elucidates that circ_0000190 suppresses TNBC progression by downregulating miR-301a and upregulating MEOX2, forming a competitive endogenous RNA (ceRNA) network of circRNA-miRNA-mRNA.
Insights
Circular RNA (circRNA) circ_0000190 suppresses triple-negative breast cancer (TNBC) progression by inhibiting miR-301a and upregulating MEOX2. This ceRNA network highlights circ_0000190 as a potential therapeutic target for TNBC.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) exhibits aggressive behavior and limited therapeutic options.
- Circular RNAs (circRNAs) and microRNAs (miRNAs) are key regulators of cancer cell processes.
- Dysregulation of circ_0000190, miR-301a, and MEOX2 is implicated in TNBC pathogenesis.
Purpose of the Study:
- To investigate the functional roles of circ_0000190, miR-301a, and MEOX2 in TNBC.
- To elucidate the molecular mechanisms underlying their interactions in TNBC progression.
- To evaluate circ_0000190 as a potential therapeutic target for TNBC.
Main Methods:
- Quantitative real-time PCR (qRT-PCR) for gene expression analysis.
- Overexpression and knockdown systems to study molecular functions.
- In vitro assays for cell proliferation, apoptosis, migration, invasion, and epithelial-mesenchymal transition (EMT).
- Mouse xenograft model for in vivo tumor growth assessment.
Main Results:
- circ_0000190 and MEOX2 were downregulated, while miR-301a was upregulated in TNBC cells.
- circ_0000190 knockdown promoted TNBC cell proliferation, migration, invasion, and EMT, and suppressed apoptosis.
- circ_0000190 acted as a sponge for miR-301a, and MEOX2 was a direct target of miR-301a.
- Overexpression of circ_0000190 inhibited tumor growth in vivo.
Conclusions:
- circ_0000190 suppresses TNBC progression by acting as a ceRNA for miR-301a and upregulating MEOX2.
- The circ_0000190/miR-301a/MEOX2 axis is a critical regulator of TNBC.
- circ_0000190 holds promise as a therapeutic target for TNBC treatment.
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