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Updated: Mar 2, 2026

DNA Vector-based RNA Interference to Study Gene Function in Cancer
Published on: June 4, 2012
YY1 directly suppresses MYCT1 leading to laryngeal tumorigenesis and progress
Si-Yao Qu1,2, Yuan-Yuan Sun1, Yun-Hui Li3
1Department of Medical Genetics, China Medical University, Shenyang, 110122, China.
Abstract:
YY1 is a key transcription factor and plays different roles in various cancers. However, role and mechanism of YY1 in laryngeal cancer are still unknown. YY1 and MYCT1 mRNA and protein levels were detected by Real-time RT-PCR and Western Blot methods, respectively. Binding of YY1 to MYCT1 promoter was predicted and confirmed by bioinformatics and chromatin immunoprecipitation assays, respectively. MYCT1 promoter activity was assessed by dual luciferase assay system. Laryngeal cancer cell proliferation, migration, and apoptosis were evaluated by cell viability, colony formation, cell scratch assay, transwell assay, and flow cytometry methods, respectively. YY1 and MYCT1 were upregulated and downregulated at transcriptional level in laryngeal cancer, respectively, which showed a negative correlation between YY1 and MYCT1 expression in laryngeal cancer. Significantly higher expression of YY1 and lower expression of MYCT1 were found in laryngeal cancer tissues of patients with lymphatic metastasis than those without metastasis.YY1 directly bound to MYCT1 promoter region and inhibited its promoter activity. YY1 silence had similar biological functions as MYCT1 overexpression in repressiveness of proliferation and migration, and promotion of apoptosis in laryngeal cancer cells. However, the effects of YY1 silence were recovered by MYCT1 knockdown. YY1 promotes proliferation and migration with suppression of apoptosis via directly inhibiting MYCT1 in laryngeal cancer cells, suggesting that YY1 is a useful target as a potential oncogene in laryngeal cancer development and progression.
Insights
The transcription factor YY1 promotes laryngeal cancer progression by inhibiting MYCT1 expression, increasing cell proliferation and migration while suppressing apoptosis. This suggests YY1 is a potential oncogene target.
Area of Science:
- Oncology
- Molecular Biology
- Cancer Genetics
Background:
- The transcription factor YY1 (Yin Yang 1) has diverse roles in various cancers, but its specific function in laryngeal cancer remains unclear.
- Understanding the molecular mechanisms underlying laryngeal cancer is crucial for developing effective therapeutic strategies.
Purpose of the Study:
- To investigate the role and mechanism of YY1 in laryngeal cancer.
- To determine the relationship between YY1 and MYCT1 expression in laryngeal cancer.
- To explore the potential of YY1 as a therapeutic target.
Main Methods:
- Quantitative real-time RT-PCR and Western Blotting were used to measure YY1 and MYCT1 mRNA and protein levels.
- Bioinformatics, chromatin immunoprecipitation, and dual-luciferase assays were employed to study the binding of YY1 to the MYCT1 promoter and its activity.
- Cell proliferation, migration, and apoptosis assays (cell viability, colony formation, scratch, Transwell, and flow cytometry) were performed to assess cellular functions.
Main Results:
- YY1 was upregulated and MYCT1 was downregulated in laryngeal cancer tissues, exhibiting a negative correlation.
- Higher YY1 and lower MYCT1 expression correlated with lymphatic metastasis in laryngeal cancer patients.
- YY1 directly bound to the MYCT1 promoter, inhibiting its activity, and YY1 knockdown reversed the effects of YY1 silence on cancer cell behavior.
Conclusions:
- YY1 acts as an oncogene in laryngeal cancer by directly inhibiting MYCT1, thereby promoting proliferation and migration while suppressing apoptosis.
- The YY1/MYCT1 axis represents a potential therapeutic target for laryngeal cancer treatment and progression management.
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