miR-548a-3p Weakens the Tumorigenesis of Colon Cancer Through Targeting TPX2
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Updated: Dec 10, 2025

Deficient Pms2, ERCC1, Ku86, CcOI in Field Defects During Progression to Colon Cancer
Published on: July 28, 2010
Ming Wang1, Min Yang2, Benyuan Deng3
1Department of General Surgery, The Third People's Hospital of Chengdu, Chengdu, China.
Abstract:
MicroRNA (miRNA) has been verified a significant factor to participate in the progression of colon cancer (CC). In this study, the authors investigated the mechanism and function of miR-548a-3p in CC. Bioinformatics analysis was used to analyze the mRNA expression profile and miRNA expression profile from GEO data series. The expression of miRNA and mRNA was analyzed by real-time quantification polymerase chain reaction in 43 pairs of CC clinical tissue samples and CC cells. The Western blot assay was used to detect the TPX2 protein. Then, SW480 and HCT116 cells were stably transfected with miR-548a-3p mimic, miR-548a-3p inhibitor, TPX2 overexpression, and TPX2 siRNA constructs to study the effects of miR-548a-3p and TPX2. Cellular functional experiments included cell counting kit-8 assay, BrdU incorporation assay, and wound healing assay. In addition, luciferase reporter assay was applied to detect the regulatory association between miR-548a-3p and TPX2. TPX2 and miR-548a-3p were identified as the interested mRNA and miRNA by microarray analysis. In CC tissues and cell lines, miR-548a-3p with low expression and TPX2 with high expression were observed. What's more, exogenous overexpressed miR-548a-3p impaired the cell viability, cell proliferation, and cell migration, while TPX2 overexpression enhanced the malignancy phenotypes. However, the promotion effect of TPX2 on CC cells was impaired by miR-548a-3p. This study revealed that miR-548a-3p attenuated the development of CC by targeting TPX2.
Insights
MicroRNA-548a-3p (miR-548a-3p) suppresses colon cancer (CC) progression by targeting the TPX2 protein. Low miR-548a-3p and high TPX2 expression correlate with CC development, with miR-548a-3p inhibiting CC cell growth and migration.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNAs (miRNAs) play a crucial role in the development and progression of colon cancer (CC).
- Understanding the specific functions and mechanisms of individual miRNAs in CC is essential for developing targeted therapies.
Purpose of the Study:
- To investigate the mechanism and function of miR-548a-3p in the progression of colon cancer.
- To determine the relationship between miR-548a-3p and its potential target gene, TPX2, in CC.
Main Methods:
- Bioinformatics analysis of GEO data series for mRNA and miRNA expression profiles.
- Real-time quantitative polymerase chain reaction (RT-qPCR) to analyze miRNA and mRNA expression in clinical CC tissues and cell lines.
- Western blot assay to detect TPX2 protein levels.
- Cellular functional assays (CCK-8, BrdU, wound healing) and luciferase reporter assay to elucidate the regulatory interaction between miR-548a-3p and TPX2.
Main Results:
- Microarray analysis identified TPX2 as a target mRNA and miR-548a-3p as a relevant miRNA in CC.
- miR-548a-3p was found to be downregulated, while TPX2 was upregulated in CC tissues and cell lines.
- Overexpression of miR-548a-3p inhibited CC cell viability, proliferation, and migration, whereas TPX2 overexpression promoted these malignant phenotypes.
- miR-548a-3p was confirmed to directly target and downregulate TPX2, thereby counteracting the pro-tumorigenic effects of TPX2.
Conclusions:
- miR-548a-3p acts as a tumor suppressor in colon cancer by targeting and inhibiting the expression of TPX2.
- The miR-548a-3p/TPX2 axis represents a potential therapeutic target for colon cancer treatment.
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