Journal of Oral Science Research ›› 2024, Vol. 40 ›› Issue (3): 236-241.DOI: 10.13701/j.cnki.kqyxyj.2024.03.009

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Prognostic Correlation Study of MYO5A Exon 35 Skipping in Head and Neck Squamous Cell Carcinoma

LU Fang1, NING Tongtong2, WANG Jie3, ZHAO Jia3, FANG Jing4, NING Qianqian3*, LI Jiafeng1,5*   

  1. 1. School of Stomatology, Xuzhou Medical University, Xuzhou 221004, China;
    2. Department of Emergency, Shandong Second Rehabilitation Hospital, Taian 271000, China;
    3. Cancer Institute, Xuzhou Medical University, Xuzhou 221004, China;
    4. Henan Institute of Science and Technology, Xinxiang 453003, China;
    5. Department of Stomatology, Affiliated Hospital of Xuzhou Medical University, Xuzhou 221006, China
  • Received:2023-11-08 Online:2024-03-28 Published:2024-03-25

Abstract: Objective: To explore the potential of MYO5A gene as a prognostic molecular marker in head and neck squamous cell carcinoma (HNSCC). Methods: RNA-Seq data and corresponding clinical data were downloaded from the TCGA database for the HNSCC queue, and the relationship between MYO5A and patient prognosis was analyzed using univariate Cox regression. The variable splicing types of the MYO5A gene were downloaded from the TCGA SpliceSeq database, the variable splicing of the differentially expressed MYO5A gene was identified based on the percentage spliced in (PSI) value, and its correlation with the prognosis of HNSCC patients was analyzed. Finally, RT-PCR and Sanger sequencing were validated in clinical samples from cell lines and affiliated hospitals of Xuzhou Medical University. Results: The MYO5A gene was significantly overexpressed in the HNSCC cohort, but the overall expression level of the MYO5A gene could not be used as an independent prognostic risk indicator for HNSCC. The frequency of MYO5A exon 35 hopping was increased in HNSCC and was closely related to prognosis. The jump of MYO5A exon 35 was validated in both cell lines and clinical samples. Conclusion: The jump of MYO5A exon 35 rather than the overall expression level of MYO5A gene can serve as an independent molecular marker for the prognosis of HNSCC.

Key words: MYO5A, head and neck squamous cell carcinoma, alternative splicing, prognosis