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Updated: Dec 14, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
circITGA7 Functions as an Oncogene by Sponging miR-198 and Upregulating FGFR1 Expression in Thyroid Cancer
Siqi Li1, Junmei Yang1, Xiaoting Liu1
1College of Life Sciences, Inner Mongolia Normal University, Hohhot, Inner Mongolia 010022, China.
Background:
Emerging evidence has indicated that circular RNAs (circRNAs), recognized as functional noncoding transcripts in eukaryotic cells, may be involved in regulating many physiological or pathological processes. However, the regulation and function of circular RNA circITGA7 in thyroid cancer (TC) remains unknown.
Methods:
In this study, we found that circITGA7 is upregulated in TC cell lines. We then performed functional analyses in the cell lines to support clinical findings. Mechanistically, we demonstrated that circITGA7 can directly bind to miR-198 and reduce the inhibition effect of miR-198 on target FGFR1 expression.
Results:
We reported an upregulation of circITGA7 in patients with TC. Silencing of circITGA7 inhibits metastasis and proliferation of TC cell lines in vitro. In addition, in the TC cell lines, the knockdown of circITGA7 or overexpression of miR-198 significantly suppressed FGFR1 levels. Mechanistically, we found that circITGA7 acts as miR-198 competitive endogenous RNA (ceRNA) to regulate FGFR1 expression.
Conclusions:
In summary, circRNA circITGA7 may play a regulatory role in TC and may be a potential marker for TC diagnosis or progression.
Insights
Circular RNA circITGA7 is upregulated in thyroid cancer (TC), promoting cancer cell metastasis and proliferation. circITGA7 acts as a ceRNA for miR-198, regulating FGFR1 expression and potentially serving as a diagnostic marker for TC.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Circular RNAs (circRNAs) are functional noncoding transcripts implicated in various biological processes.
- The specific role of circRNA circITGA7 in thyroid cancer (TC) pathogenesis was previously uncharacterized.
Purpose of the Study:
- To investigate the expression, function, and mechanism of circRNA circITGA7 in thyroid cancer.
Main Methods:
- Quantitative analysis of circITGA7 expression in TC cell lines and patient samples.
- In vitro functional assays including cell proliferation and metastasis assays.
- Mechanistic studies involving circRNA-miRNA interactions and target gene expression analysis.
Main Results:
- circITGA7 was found to be significantly upregulated in TC cell lines and patient tissues.
- Silencing circITGA7 inhibited proliferation and metastasis of TC cell lines.
- circITGA7 functions as a miR-198 sponge, competitively binding to miR-198 and thereby increasing the expression of its target gene, FGFR1.
Conclusions:
- circRNA circITGA7 plays a crucial role in promoting thyroid cancer progression.
- circITGA7 may serve as a potential biomarker for the diagnosis and monitoring of thyroid cancer.
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