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Updated: Aug 5, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
Autophagy-Related MicroRNA: Tumor miR-125b and Thyroid Cancers
Liudmila V Spirina1,2, Irina V Kovaleva1,2, Svetlana Yu Chizhevskaya1,2
1Ministry of Health of Russia, Siberian State Medical University, 634050 Tomsk, Russia.
Background:
Autophagy is a stress response mechanism that causes cellular components to degrade. Its defects were associated with multiple pathologies, including cancers. Thyroid cancer is known to be the most prevalent form of malignant neoplasm among endocrine tumors. The aim of the study was to seek and comprehensively explore the role of autophagy related genes and proteins play in thyroid cancers through bioinformatics analysis with their detection in the tissue samples.
Methods:
Bioinformatics analysis was performed to investigate autophagy related proteins and genes involvement in thyroid cancer progression. The experimental verification was done in cancer samples of one hundred and three patients with thyroid pathology included in the study. The miR-125blevel was detected by PCR in real time.
Results And Discussion:
The bioinformatics analysis verified the miR-125b as a regulatory mechanism in autophagy. Its expression in patients with PTC was reduced by 6.75 times in cancer patients compared to the patients with benign tumors. The BRAFV600E mutations were associated with a decrease in hsa-miR-125b expression by 12.67 times compared to tumors with the wild-type gene.
Conclusions:
Our findings revealed involvement of the autophagy related proteins in cancer progression. The significant mechanisms of regulation are non-coding RNA sequences implicated in a variety of oncogenic processes. We found that miR-125b is a potential maker in thyroid cancer invasion, BRAV600E mutational status and risk of recurrence.
Insights
Autophagy plays a role in thyroid cancer. MicroRNA-125b (miR-125b) is a potential biomarker for thyroid cancer invasion and recurrence risk, especially in patients with BRAFV600E mutations.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Autophagy, a cellular degradation process, is linked to various pathologies, including cancer.
- Thyroid cancer is the most common endocrine malignancy.
- Defects in autophagy are implicated in cancer development and progression.
Purpose of the Study:
- To investigate the role of autophagy-related genes and proteins in thyroid cancer.
- To explore the regulatory mechanisms of autophagy in thyroid cancer through bioinformatics and experimental analysis.
- To identify potential biomarkers for thyroid cancer progression and recurrence.
Main Methods:
- Bioinformatics analysis of autophagy-related genes and proteins in thyroid cancer.
- Experimental verification using tissue samples from 103 thyroid cancer patients.
- Real-time PCR detection of microRNA-125b (miR-125b) expression levels.
Main Results:
- Bioinformatics analysis identified miR-125b as a key regulator of autophagy in thyroid cancer.
- miR-125b expression was significantly reduced (6.75-fold) in papillary thyroid cancer (PTC) compared to benign tumors.
- Reduced miR-125b expression (12.67-fold) was associated with BRAFV600E mutations in thyroid tumors.
Conclusions:
- Autophagy-related proteins are involved in thyroid cancer progression.
- Non-coding RNAs, such as miR-125b, are significant regulatory mechanisms in oncogenesis.
- miR-125b is a potential biomarker for thyroid cancer invasion, BRAFV600E mutational status, and recurrence risk.
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