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Updated: Dec 26, 2025

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
Published on: March 14, 2019
Hsa_circ_0137008 suppresses the malignant phenotype in colorectal cancer by acting as a microRNA-338-5p sponge
Zhanfeng Yang1, Jingjing Zhang1, Danghui Lu2
11Department of Medicine, Zhengzhou University of Industry Technology, 16 Xueyuan Road, Xinzheng, 451100 Henan China.
Background:
Circular RNAs (circRNAs) have been shown to play a crucial role in tumorigenesis. In this study, we investigated the function of hsa_circ_0137008 and its underlying molecular mechanism in colorectal cancer (CRC).
Methods:
Gene expression was conducted by quantitative real-time PCR or western blot. Functional experiments were performed by cell count kit-8, colony formation assay, wound healing, and transwell assays. Luciferase reporter assay and RNA pull-down assay were performed to investigate the molecular mechanism of hsa_circ_0137008 in CRC. In addition, the xenograft tumor model was applied to determine the role of hsa_circ_0137008 in vivo.
Results:
Downregulation of hsa_circ_0137008 was observed in CRC tissues and cell lines. Functionally, overexpression of hsa_circ_0137008 inhibited the proliferation of CRC cells, as indicated by the inhibition of proliferative protein expression (Ki67 and PCNA), reduced cell viability and colony formation ability. Upregulation of hsa_circ_0137008 suppressed the migration, invasion, and epithelial to mesenchymal transition (EMT) of CRC cells. Mechanically, hsa_circ_0137008 negatively regulated the expression of microRNA-338-5p (miR-338-5p). Furthermore, hsa_circ_0137008 abated the miR-338-5p mediated promotion on CRC cell progression. Tumor suppressive function of hsa_circ_0137008 was validated in vivo.
Conclusion:
These findings highlighted the fact that overexpression of hsa_circ_0137008 inhibited the progression of CRC via sponging miR-338-5p, suggesting that hsa_circ_0137008/miR-338-5p axis is a principal regulator of CRC tumorigenesis.
Insights
Overexpression of circular RNA hsa_circ_0137008 inhibits colorectal cancer (CRC) progression by sponging microRNA-338-5p. This hsa_circ_0137008/miR-338-5p axis acts as a key regulator in CRC tumorigenesis.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Circular RNAs (circRNAs) are implicated in cancer development.
- The specific role of hsa_circ_0137008 in colorectal cancer (CRC) tumorigenesis requires elucidation.
Purpose of the Study:
- To investigate the function of hsa_circ_0137008 in colorectal cancer (CRC).
- To explore the molecular mechanism underlying hsa_circ_0137008's role in CRC.
Main Methods:
- Quantitative real-time PCR and Western blot for gene expression analysis.
- In vitro assays (cell count, colony formation, wound healing, Transwell) to assess cell proliferation, viability, migration, and invasion.
- Luciferase reporter and RNA pull-down assays to determine molecular interactions.
- In vivo xenograft tumor model to evaluate the role of hsa_circ_0137008.
Main Results:
- hsa_circ_0137008 was downregulated in CRC tissues and cell lines.
- Overexpression of hsa_circ_0137008 suppressed CRC cell proliferation, migration, invasion, and epithelial-mesenchymal transition (EMT).
- hsa_circ_0137008 acts as a sponge for microRNA-338-5p (miR-338-5p), inhibiting its pro-tumorigenic effects in CRC.
Conclusions:
- Overexpression of hsa_circ_0137008 inhibits CRC progression by sponging miR-338-5p.
- The hsa_circ_0137008/miR-338-5p axis is a critical regulator of colorectal cancer tumorigenesis.
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