China Journal of Oral and Maxillofacial Surgery ›› 2023, Vol. 21 ›› Issue (5): 439-445.doi: 10.19438/j.cjoms.2023.05.003

• Original Articles • Previous Articles     Next Articles

The impact of mitochondrial topoisomerase I expression in head and neck squamous cell carcinoma

ZHAI Pei-song1, TONG Tong2, LIU Chun1, MA Hai-long1, ZHANG Jian-jun1   

  1. 1. Department of Oromaxillofacial Head and Neck Oncology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine; College of Stomatology, Shanghai Jiao Tong University; National Center for Stomatology; National Clinical Research Center for Oral Diseases; Shanghai Key Laboratory of Stomatology; Shanghai Research Institute of Stomatology; Shanghai Center of Head and Neck Oncology Clinical and Translational Science. Shanghai 200011;
    2. Department of Oromaxillofacial Surgery, Shanghai Stomatological Hospital & School of Stomatology, Fudan University; Shanghai Key Laboratory of Craniomaxillofacial Development and Diseases, Fudan University. Shanghai 200001, China
  • Received:2023-05-19 Revised:2023-07-17 Online:2023-09-20 Published:2023-10-11

Abstract: PURPOSE: To analyze the correlation between mitochondrial topoisomerase I (TOP1MT) and the clinicopathological characteristics of head and neck squamous cell carcinoma(HNSCC), and to explore its impact on cisplatin resistance in HNSCC. METHODS: The correlation between TOP1MT and clinicopathological characteristics was analyzed by combining the information of 83 clinical patients with the results of immunohistochemical staining and real-time fluorescence quantitative PCR(qRT-PCR). The effect of TOP1MT on proliferation and migration of HNSCC cells with cisplatin treatment was analyzed by in vitro experiments. SPSS 26.0 software package was used for statistical analysis. RESULTS: High expressed TOP1MT was related to tumor size, clinical stage, overall survival, efficacy of TPF regimen, and worse prognosis of HNSCC patients, and the survival probability of patients with high expression of TOP1MT was significantly lower than that of patients with moderate and low expression. In vitro experiments showed that overexpression of TOP1MT significantly promoted the migration and proliferation of HNSCC cells HN30 and HN4 with 20 μmol/L cisplatin treatment. CONCLUSIONS: High expression of TOP1MT in HNSCC indicates insensitivity to chemotherapy and decreased overall survival. The experiment confirmed that TOP1MT promotes HNSCC development and may act as a potential target for clinical therapy.

Key words: TOP1MT, Head and neck squamous cell carcinoma, Cisplatin, Chemoresistance

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