Related Experiment Video
Updated: Sep 1, 2025

In Vivo Inhibition of MicroRNA to Decrease Tumor Growth in Mice
Published on: August 23, 2019
TBX3 activating PVT1 accelerates proliferation, migration, and invasion by modulating the miR-30a/LOX axis in
Jing Wen1,2, Wei Zhang3, Yan Zhou2
1Department of Ultrasound Centre, Affiliated Hospital of Guizhou Medical University, Guiyang, Guizhou, China.
Introduction:
Anaplastic thyroid carcinoma (ATC) is a nearly chemo-resistant malignancy with high invasion and mortality. Long non-coding RNAs (lncRNAs) have been demonstrated to be dysregulated and play a crucial role in the development and process of ATC. The present study aimed to explore the mechanism of PVT1 dysregulation in ATC.
Material And Methods:
The mRNA levels of PVT1 and T-box3 (TBX3), and the protein levels of TBX3 in ATC and paracancerous tissues, and FRO and Nthy-ori 3-1 cells were determined by quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) and western blot, respectively. The transcriptional factor binding site was predicted and validated between TBX3 and PVT1 promoter through the JASPAR website, and ChIP and luciferase analysis. The proliferation, migration, and invasion of FRO cells were assessed by MTT, colony formation, and transwell assays.
Results:
PVT1 expression was upregulated in ATC, which was positively correlative with the level of transcription factor TBX3. Downregulation of PVT1 inhibited the proliferation, migration, and invasion of FRO cells. Moreover, TBX3 targeting the promoter region of PVT1 promoted the expression level of PVT1 and modulated the downstream signalling axis of PVT1, miR-30a/LOX. Also, interference of PVT1 reversed the stimulative role of overexpression of TBX3 in the progress of FRO cells.
Conclusion:
TBX3 enhanced proliferation, migration, and invasion of ATC cells via activation of PVT1 and modulation of the miR-30a/LOX signalling axis.
Insights
The transcription factor TBX3 promotes anaplastic thyroid carcinoma (ATC) progression by upregulating the long non-coding RNA PVT1. This pathway involves the miR-30a/LOX signaling axis, impacting cell proliferation, migration, and invasion.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Anaplastic thyroid carcinoma (ATC) is an aggressive cancer with poor prognosis.
- Long non-coding RNAs (lncRNAs) are implicated in ATC development and progression.
- Understanding the regulatory mechanisms of lncRNAs in ATC is crucial for therapeutic strategies.
Purpose of the Study:
- To investigate the role and mechanism of PVT1 dysregulation in anaplastic thyroid carcinoma.
- To elucidate the relationship between transcription factor TBX3 and PVT1 expression in ATC.
- To explore the downstream signaling pathway regulated by TBX3 and PVT1.
Main Methods:
- Quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) and western blot were used to measure PVT1 and TBX3 levels.
- Bioinformatic tools (JASPAR) and experimental assays (ChIP, luciferase) validated TBX3 binding to the PVT1 promoter.
- Cellular assays (MTT, colony formation, transwell) assessed the impact of PVT1 on cell proliferation, migration, and invasion.
Main Results:
- PVT1 expression was significantly upregulated in ATC tissues and correlated with TBX3 levels.
- Downregulation of PVT1 suppressed proliferation, migration, and invasion of ATC cells.
- TBX3 directly targeted the PVT1 promoter, enhancing PVT1 expression and modulating the PVT1/miR-30a/LOX axis.
Conclusions:
- TBX3 acts as a positive regulator of ATC cell proliferation, migration, and invasion.
- The TBX3-PVT1 axis plays a critical role in ATC pathogenesis.
- Targeting the TBX3-PVT1-miR-30a/LOX pathway may offer a therapeutic strategy for ATC.
Related Concept Videos
Abnormal Proliferation
mTOR Signaling and Cancer Progression
The mTOR pathway or the...
PI3K/mTOR/AKT Signaling Pathway
Regulation of Angiogenesis and Blood Supply
TGF - β Signaling Pathway
Synthesis and Regulation of Thyroid Hormones
Upon reaching the thyroid gland, TSH stimulates the follicular cells' active uptake of iodide ions from the blood. The ions diffuse to the apical surface of the cells and are oxidized to iodine. The...

