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Updated: Mar 21, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA‑126 is downregulated in thyroid cancer cells, and regulates proliferation, migration and invasion by
Yan Qian1, Xiaoli Wang2, Zhanlu Lv1
1Department of Environmental Pollution and Health, State Key Laboratory of Environmental Criteria and Risk Assessment, Chinese Research Academy of Environmental Sciences, Beijing 100012, P.R. China.
Abstract:
MicroRNA-126 (miR-126) has previously been reported to be downregulated in various types of cancer; however, at present, there are no studies of miR‑126 in human thyroid cancer. The present study aimed to determine the expression and effects of miR‑126 on thyroid cancer. The expression levels of miR‑126 were detected in human thyroid cancer tissues, matched normal adjacent tissues and human thyroid cancer cell lines using quantitative polymerase chain reaction. In addition, post‑transfection of human thyroid cancer cells with miR‑126 mimics, cell proliferation, migration and invasion assays, western blot analysis and luciferase assays were conducted. The results demonstrated that miR‑126 was downregulated in thyroid cancer tissues and cells. Furthermore, upregulation of miR‑126 inhibited cell proliferation, migration and invasion in thyroid cancer cells. The present study also provided evidence suggesting that miR‑126 may directly target C‑X‑C chemokine receptor type 4 (CXCR4) in thyroid cancer. These results indicated that miR‑126 may be investigated as a target for the treatment of thyroid cancer.
Insights
MicroRNA-126 (miR-126) is downregulated in thyroid cancer, inhibiting cancer cell proliferation, migration, and invasion. This suggests miR-126 could be a potential therapeutic target for thyroid cancer treatment.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- MicroRNA-126 (miR-126) is known to be downregulated in several cancers.
- Its role in human thyroid cancer has not been previously investigated.
Purpose of the Study:
- To determine the expression levels of miR-126 in human thyroid cancer.
- To investigate the functional effects of miR-126 on thyroid cancer cell behavior.
- To identify potential molecular targets of miR-126 in thyroid cancer.
Main Methods:
- Quantitative polymerase chain reaction (qPCR) to measure miR-126 expression in tumor tissues and cell lines.
- Cell proliferation, migration, and invasion assays.
- Western blot analysis and luciferase assays to confirm direct targeting of C-X-C chemokine receptor type 4 (CXCR4).
Main Results:
- miR-126 expression was significantly downregulated in thyroid cancer tissues and cell lines compared to normal controls.
- Upregulation of miR-126 using mimics suppressed thyroid cancer cell proliferation, migration, and invasion.
- miR-126 was found to directly target CXCR4 in thyroid cancer cells.
Conclusions:
- miR-126 plays an inhibitory role in thyroid cancer progression.
- The findings suggest that miR-126, by targeting CXCR4, could serve as a novel therapeutic target for thyroid cancer.
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