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Updated: Dec 25, 2025

Analysis of Combinatorial miRNA Treatments to Regulate Cell Cycle and Angiogenesis
Published on: March 30, 2019
miR-143 inhibits renal cell carcinoma cells metastatic potential by suppressing ABL2
Bin Xu1, Can Wang1, Ya-Li Wang1
1Department of Urology, Affiliated Zhongda Hospital of Southeast University, Nanjing, China.
Abstract:
Although micro RNA (miRNA) expression profiles are widely investigated in renal cell carcinoma (RCC), their potential roles for affecting RCC initiation and progression remain largely unknown. Here, we examined the aberrant expression profiles of miRNAs inhuman metastatic RCC tissues based on Gene Expression Omnibus (GSE37989). We further validated them iRNAs expression data in the largest clinical dataset: The Cancer Genome Atlas (TCGA). And cell adhesion and migration abilities and epithelial me senchymal transition (EMT) related proteins were assessed in both normal and tumor RCC cell lines. We suggest that hsa-miR-143 is a potential tumor suppressor in RCC as its down regulation positively correlated with adverse prognosis. Biologically, cell adhesion, migration, and EMT were dramatically inhibited by miR-143. Mechanistically, we found that miR-143 targets ABL proto-oncogene 2 (ABL2), which was also found to be an indicator for poor survival in TCGA database. Our results have important implications in understanding functions of miRNAs in metastatic RCC and will provide a basis for further clinical application.
Insights
MicroRNA (miRNA) hsa-miR-143 acts as a tumor suppressor in renal cell carcinoma (RCC). Its downregulation correlates with poor prognosis, inhibiting cancer cell adhesion, migration, and epithelial-mesenchymal transition (EMT).
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA (miRNA) expression is altered in renal cell carcinoma (RCC), but their functional roles in cancer initiation and progression are not fully understood.
- Investigating miRNA profiles is crucial for understanding metastatic RCC pathogenesis.
Purpose of the Study:
- To identify aberrant miRNA expression profiles in metastatic RCC.
- To elucidate the functional and mechanistic roles of specific miRNAs in RCC progression.
- To explore potential therapeutic targets for RCC.
Main Methods:
- Analysis of miRNA expression data from Gene Expression Omnibus (GSE37989) and The Cancer Genome Atlas (TCGA) datasets.
- Assessment of cell adhesion, migration, and epithelial-mesenchymal transition (EMT) in RCC cell lines.
- Target validation of miRNA-gene interactions.
Main Results:
- Downregulation of hsa-miR-143 was observed in metastatic RCC and correlated with adverse prognosis.
- Overexpression of miR-143 significantly inhibited cell adhesion, migration, and EMT.
- ABL proto-oncogene 2 (ABL2) was identified as a direct target of miR-143, and its high expression indicated poor survival in RCC patients.
Conclusions:
- hsa-miR-143 functions as a tumor suppressor in RCC by targeting ABL2.
- miR-143 plays a critical role in regulating cell adhesion, migration, and EMT in RCC.
- These findings provide insights into miRNA functions in metastatic RCC and suggest miR-143 as a potential therapeutic target.
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