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Updated: Jan 6, 2026

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
MicroRNA-1271 inhibits the progression of papillary thyroid carcinoma by targeting IRS1 and inactivating AKT pathway
1Department of Breast, Thyroid Surgery, Research Institute of Surgery, Daping Hospital, Army Military Medical University, Chongqing, China. luodl968@163.com.
Objective:
The important role of microRNA-1271 (miR-1271) has been identified in human diseases and cancers. However, the biological function of miR-1271 remains ambiguous in papillary thyroid carcinoma (PTC). Therefore, the specific role of miR-1271 was investigated in PTC.
Patients And Methods:
The expressions of miR-1271 and insulin receptor substrate 1 (IRS1) were detected by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR) assay. The protein expression of the genes was measured by Western blot analysis. The function of miR-1271 was investigated using methyl thiazolyl tetrazolium (MTT) and transwell assays. The Dual-Luciferase assay was used to observe the relationship between miR-1271 and IRS1.
Results:
MiR-1271 was downregulated in PTC tissues. Moreover, overexpression of miR-1271 suppressed migration, invasion and proliferation of PTC cells. Furthermore, IRS1 was indicated as a direct target gene of miR-1271 and knockdown of IRS1 inhibited cell migration, invasion and proliferation in PTC. In addition, miR-1271 inhibited the progression of PTC by targeting IRS1. Besides that, miR-1271 blocked the epithelial-mesenchymal transition (EMT) and protein kinase B (AKT) pathway in PTC.
Conclusions:
MiR-1271 inhibited the progression of PTC by targeting IRS1 and blocking EMT and AKT pathway.
Insights
MicroRNA-1271 (miR-1271) suppresses papillary thyroid carcinoma (PTC) progression by targeting insulin receptor substrate 1 (IRS1). This inhibition blocks epithelial-mesenchymal transition (EMT) and the AKT pathway, offering therapeutic potential for PTC.
Area of Science:
- Molecular Biology
- Oncology
- Biochemistry
Background:
- MicroRNA-1271 (miR-1271) is implicated in various human diseases and cancers.
- The specific role of miR-1271 in papillary thyroid carcinoma (PTC) requires clarification.
Purpose of the Study:
- To investigate the biological function and mechanism of miR-1271 in papillary thyroid carcinoma (PTC).
Main Methods:
- Quantitative Real-Time Polymerase Chain Reaction (qRT-PCR) and Western blot were used to measure gene and protein expression.
- Methyl thiazolyl tetrazolium (MTT) and transwell assays assessed cell proliferation, migration, and invasion.
- Dual-Luciferase assay confirmed the direct targeting relationship between miR-1271 and insulin receptor substrate 1 (IRS1).
Main Results:
- MiR-1271 expression was significantly downregulated in PTC tissues.
- Overexpression of miR-1271 suppressed PTC cell proliferation, migration, and invasion.
- Insulin receptor substrate 1 (IRS1) was identified as a direct target of miR-1271; IRS1 knockdown mimicked miR-1271's suppressive effects.
- MiR-1271 was found to inhibit PTC progression by targeting IRS1, consequently blocking the epithelial-mesenchymal transition (EMT) and the protein kinase B (AKT) pathway.
Conclusions:
- MiR-1271 acts as a tumor suppressor in PTC.
- The mechanism involves targeting IRS1, thereby inhibiting EMT and the AKT pathway.
- MiR-1271 represents a potential therapeutic target for papillary thyroid carcinoma.
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