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Updated: Sep 25, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-873-5p suppresses cell malignant behaviors of thyroid cancer via targeting CXCL5 and regulating P53 pathway
Wang Chang1, Qing Chang1, Haodong Lu1
1Department of Head and Neck Surgery, Tangshan Gongren Hospital, Tangshan, Hebei Province, China.
Abstract:
We aimed to examine the roles of microRNA-873-5p and CXCL5 in thyroid cancer (TC) cells. qRT-PCR was adopted to measure the expression levels of CXCL5 mRNA and microRNA-873-5p in TC cells, and western blot was adopted to evaluate the CXCL5 protein expression level. Bioinformatics analysis was done to predict the upstream gene of CXCL5. Dual-luciferase assay was applied to validate the binding relationship of CXCL5 and the upstream regulatory gene. Cell experiments were done to detect the effects of microRNA-873-5p targeting CXCL5 on malignant progression of cancer cells. Western blot was adopted to demonstrate the phosphorylation level of P53 pathway related-proteins. CXCL5 was upregulated in TC cells and tissues. The results of in vitro assays displayed that CXCL5 downregulation dramatically suppressed the malignant behaviors of TC cells. MicroRNA-873-5p suppressed CXCL5 expression, but the suppressive effect of microRNA-873-5p on TC cells was abolished through CXCL5 overexpression. Additionally, microRNA-873-5p could mediate p53 pathway and thereby inhibit the malignant behaviors of TC cells through targeting CXCL5. In summary, we proved that microRNA-873-5p repressed the malignant behaviors of TC cells through targeting CXCL5 and P53 pathway, indicating that microRNA-873-5p can be a biomarker for TC.
Insights
MicroRNA-873-5p inhibits thyroid cancer (TC) progression by targeting CXCL5 and the P53 pathway. This study identifies microRNA-873-5p as a potential biomarker for TC diagnosis and treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Thyroid cancer (TC) progression involves complex molecular mechanisms.
- Identifying key regulatory factors like microRNAs and chemokines is crucial for understanding TC pathogenesis.
Purpose of the Study:
- To investigate the roles of microRNA-873-5p and CXCL5 in thyroid cancer (TC) cells.
- To elucidate the regulatory relationship between microRNA-873-5p, CXCL5, and the P53 pathway in TC.
- To assess the potential of microRNA-873-5p as a diagnostic biomarker for TC.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (qRT-PCR) for gene and microRNA expression analysis.
- Western blot to assess protein expression and P53 pathway activation.
- Bioinformatics analysis and dual-luciferase assay to predict and validate regulatory interactions.
- In vitro cell experiments to evaluate the functional impact of microRNA-873-5p and CXCL5 on TC cell behavior.
Main Results:
- CXCL5 expression was significantly upregulated in TC cells and tissues.
- Downregulation of CXCL5 suppressed malignant behaviors of TC cells.
- MicroRNA-873-5p suppressed CXCL5 expression, and this effect was reversed by CXCL5 overexpression.
- MicroRNA-873-5p targeted CXCL5, modulated the P53 pathway, and inhibited TC cell malignancy.
Conclusions:
- MicroRNA-873-5p exerts its anti-cancer effects in TC by targeting CXCL5 and influencing the P53 pathway.
- The microRNA-873-5p/CXCL5/P53 axis represents a novel regulatory mechanism in thyroid cancer.
- MicroRNA-873-5p holds promise as a potential biomarker for thyroid cancer.
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