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Published on: March 18, 2020
PRR4: A novel downregulated gene in laryngeal cancer
Seda Ekizoglu1, Turgut Ulutin1, Jalal Guliyev2
1Department of Medical Biology, Cerrahpasa Medical Faculty, Istanbul University, Istanbul 34098, Turkey.
Abstract:
Head and neck squamous cell carcinomas (HNSCC) are a diverse group of tumor types, including neoplasia of the paranasal sinuses, oral cavity, trachea, pharynx and larynx. Laryngeal cancer is the most common type of HNSCC. The proline-rich 4 (PRR4) protein is synthesized in the acinar cells of human lacrimal glands. Previous studies have demonstrated that PRR4 may function as an antimicrobial protein protecting the ocular surface and the oral cavity. In order to determine differentially expressed genes (DEGs) in laryngeal tumors, a GeneFishing Assay was performed; 27 DEGs were identified. The PRR4 gene expression level in laryngeal tissue samples obtained from 90 patients, and the saliva of 25 healthy smokers and 25 non-smokers, was investigated using reverse transcription-quantitative polymerase chain reaction. It was revealed that PRR4 gene expression was decreased in 65/90 tumor tissues (72.2%) compared with normal tissues. No significant difference was identified between the healthy smoker and the non-smoker groups in terms of PRR4 gene expression. The results of the present study indicated that the PRR4 gene may serve an important role in laryngeal carcinogenesis.
Insights
Proline-rich 4 (PRR4) gene expression significantly decreases in most laryngeal tumors, suggesting its potential role in preventing head and neck squamous cell carcinoma development. Smoking status did not impact PRR4 levels in healthy individuals.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Head and neck squamous cell carcinomas (HNSCC) encompass various tumors, with laryngeal cancer being the most prevalent.
- Proline-rich 4 (PRR4) protein, synthesized in lacrimal glands, is known for potential antimicrobial functions in ocular and oral surfaces.
- Previous research suggests PRR4's protective roles, but its involvement in laryngeal carcinogenesis remains unexplored.
Purpose of the Study:
- To investigate the differential expression of genes in laryngeal tumors.
- To determine the role of the proline-rich 4 (PRR4) gene in laryngeal carcinogenesis.
- To analyze PRR4 gene expression in laryngeal tissues and saliva samples.
Main Methods:
- GeneFishing Assay was employed to identify differentially expressed genes (DEGs) in laryngeal tumors.
- Reverse transcription-quantitative polymerase chain reaction (RT-qPCR) was used to quantify PRR4 gene expression.
- Laryngeal tissue samples from 90 patients and saliva from 50 healthy individuals (25 smokers, 25 non-smokers) were analyzed.
Main Results:
- A GeneFishing Assay identified 27 differentially expressed genes (DEGs) in laryngeal tumors.
- PRR4 gene expression was significantly decreased in 72.2% (65/90) of laryngeal tumor tissues compared to normal tissues.
- No significant difference in PRR4 gene expression was observed between healthy smokers and non-smokers.
Conclusions:
- The PRR4 gene exhibits decreased expression in a majority of laryngeal tumors.
- These findings suggest that reduced PRR4 expression may be implicated in the development of laryngeal cancer.
- PRR4 warrants further investigation as a potential biomarker or therapeutic target in head and neck squamous cell carcinoma.
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