West China Journal of Stomatology ›› 2015, Vol. 33 ›› Issue (6): 575-580.doi: 10.7518/hxkq.2015.06.005

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Myeloid-derived suppressor cell expression and significance in peripheral blood and tongue lesions of mouse

Chu Mei1, Liao Guiqing2, Tang Wen1, Zhou Yuan1, Su Yuxiong3, Liang Yujie2   

  1. 1. Dept. of Stomatology, Guangzhou Number 8 People’s Hospital, Guangzhou 510440, China; 2. Dept. of Oral and Maxillofacial Surgery, Guanghua School of Stomatology, Hospital of Stomatology, Sun Yat-Sen University, Guangzhou 510055, China; 3. Dept. of Oral and Maxillofacial Surgery, Faculty of Dentistry, The University of Hong Kong, Hong Kong 999077, China)
  • Received:2015-04-23 Revised:2015-09-06 Online:2015-12-01 Published:2015-12-01

Abstract: Objective To explore the myeloid-derived suppressor cell (MDSC) expression in the peripheral blood and lesions of 4NQO-induced tongue carcinoma in mouse. Methods The established 4NQO mouse model was used to analyze the distribution of MDSC and T cell subsets in the peripheral blood by flow cytometry. The relations of MDSC with T cell subsets and CD4+/CD8+ changes were evaluated. The distribution of MDSC in the lesions of tongues was analyzed by immunohistochemistry, and the expression of arginase 1 (ARG-1) in tongue tissues was detected by real-time polymerase chain reaction. Results During tumor progression, a significant increase was observed in the frequency of MDSC in the peripheral blood of 4NQO treated mice (P<0.01). The frequency of MDSC was positively correlated with systemic CD3+CD8+T cells but negatively correlated with the CD4+/CD8+ ratio. Squamous cell carcinomas were extensively infiltrated with MDSC, whereas dysplastic area and normal tongue mucosa had only sparse MDSC infiltration. The majority of MDSCs were located in the stroma, particularly along the tumor invasive front. Moreover, 4NQO-treated mice showed significantly higher ARG-1 mRNA levels in the tumor site (P<0.01). Conclusion MDSC may contribute to oral tumor progression and represents a potential target for immunotherapy of oral cancer.

Key words: squamous cell carcinoma, myeloid-derived suppressor cell, immunosuppression

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