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Author Spotlight: Unlocking the Mysteries of Oral Potential Malignancies
Published on: August 11, 2023
Aberrant DNA hypermethylation-silenced SOX21-AS1 gene expression and its clinical importance in oral cancer
Cheng-Mei Yang1, Tsung-Han Wang2, Hung-Chih Chen1
1Department of Stomatology, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan ; Department of Dental Technology, Shu-Zen Junior College of Medicine and Management, Kaohsiung, Taiwan.
Background:
Long noncoding RNAs (lncRNAs) are more than 200 nucleotides in length and lack transcriptional ability. The biological function of lncRNAs in oral squamous cell carcinoma (OSCC) remains unclear. The aim of this study was to identify the dysfunction of lncRNA in OSCC.
Results:
We analyzed the transcriptome profiles of human OSCC tissues and paired adjacent normal tissues from two patients through a next-generation sequencing approach. A total of 14 lncRNAs were upregulated (fold change ≥3) and 13 were downregulated (fold change ≤-3) in OSCC tissues compared with the adjacent normal tissues. SOX21-AS1 was subjected to further analysis, revealing that the expression levels of SOX21-AS1 significantly decreased in OSCC compared with the adjacent normal tissue. The promoter activity of SOX21-AS1 was obviously suppressed by in vitro methylation. The DNA methylation status of the SOX21-AS1 promoter was analyzed using combined bisulfite restriction analysis, revealing that the aberrant promoter hypermethylation of SOX21-AS1 was observed frequently in OSCC tissues. The effects of SOX21-AS1 on cell proliferation and invasion were examined through transient transfection. Our data showed that SOX21-AS1 could significantly suppress oral cancer cell growth and invasion. Furthermore, the low expression level of SOX21-AS1 was significantly correlated with an advanced stage (P = 0.047), large tumor size (P = 0.033), and poor disease-specific survival in OSCC patients (P = 0.002).
Conclusions:
SOX21-AS1 was identified as susceptible dysfunction correlated with promoter hypermethylation in OSCC. Low SOX21-AS1 expression may be an adverse prognostic biomarker for OSCC.
Insights
Long noncoding RNA SOX21-AS1 is downregulated in oral squamous cell carcinoma due to promoter hypermethylation. Reduced SOX21-AS1 expression indicates a poor prognosis for OSCC patients.
Area of Science:
- Molecular Biology
- Oncology
- Genetics
Background:
- Long noncoding RNAs (lncRNAs) are critical in cellular processes, but their role in oral squamous cell carcinoma (OSCC) is not fully understood.
- This study investigates the functional significance of lncRNAs in OSCC development and progression.
Purpose of the Study:
- To identify dysregulated long noncoding RNAs (lncRNAs) in oral squamous cell carcinoma (OSCC).
- To investigate the role of the lncRNA SOX21-AS1 in OSCC pathogenesis and its potential as a prognostic biomarker.
Main Methods:
- Transcriptome profiling of OSCC tissues and adjacent normal tissues using next-generation sequencing.
- Analysis of SOX21-AS1 expression, promoter activity, and DNA methylation status.
- Functional assays (transient transfection) to assess the impact of SOX21-AS1 on cell proliferation and invasion.
Main Results:
- 14 lncRNAs were upregulated and 13 downregulated in OSCC tissues.
- SOX21-AS1 expression was significantly decreased in OSCC, associated with promoter hypermethylation.
- SOX21-AS1 suppressed oral cancer cell growth and invasion.
- Low SOX21-AS1 expression correlated with advanced stage, larger tumor size, and poorer survival in OSCC patients.
Conclusions:
- SOX21-AS1 dysfunction, driven by promoter hypermethylation, is implicated in OSCC.
- Reduced SOX21-AS1 expression serves as a potential adverse prognostic biomarker for oral squamous cell carcinoma.
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