Shanghai Journal of Stomatology ›› 2026, Vol. 35 ›› Issue (3): 252-257.doi: 10.19439/j.sjos.2026.03.005

• Original Articles • Previous Articles     Next Articles

Research on hypoxia-mediated macrophage polarization during the carcinogenesis of oral leukoplakia

Zhao Xiaoxian1,3, Zhang Chunye2,3, Zhao Zhengyan1,3, Zhang Ying1,3, Wu Lan1,3   

  1. 1. Department of Oral Mucosal Diseases, 2. Department of Oral Pathology, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine; 3. College of Stomatology, Shanghai Jiao Tong University, Shanghai Key Laboratory of Stomatology, National Center for Stomatology, National Clinical Research Center for Oral Diseases, Shanghai Research Institution of Stomatology. Shanghai 200011, China
  • Received:2025-03-03 Revised:2025-05-12 Published:2026-07-02

Abstract: PURPOSE: To investigate the expression level of hypoxia-inducible factor-1α (HIF-1α) and its impact on macrophage polarization in the immune microenvironment during carcinogenesis of oral leukoplakia (OLK). METHODS: This study employed multiplex immunofluorescence to retrospectively analyze HIF-1α, inducible nitric oxide synthase (iNOS), and CD206 expression in 25 OLK and normal mucosal tissue samples. An in vitro co-culture system was conducted under hypoxic conditions with Leuk-1 and Raw 264.7 cells. Macrophage polarization dynamics were quantitatively assessed by detection of HIF-1α, iNOS, and CD206 expression levels. Subsequently, inhibitor of HIF-1α was used to validate its regulatory role. RESULTS: In a cohort of 25 OLK and normal mucosal tissue samples, iNOS+ cells demonstrated initial elevation during mild dysplasia but significantly decreased in severe dysplasia and oral squamous cell carcinoma (OSCC). Conversely, CD206+ and HIF-1α+ cells exhibited progressive accumulation throughout OLK malignant transformation. Macrophage polarization analysis revealed M1 polarization (CD206/iNOS ratio: 0.68±0.22 to 0.69±0.41) was presented in mild-to-moderate dysplasia, with marked M2 polarization emerging in advanced stages (3.27±1.64 to 5.82±1.32). Correlation analyses identified progressively strengthened associations between HIF-1α and CD206, iNOS, and M2 polarization during disease progression. In vitro experiments under hypoxic conditions confirmed positive correlations between HIF-1α expression and CD206/iNOS levels as well as M2 polarization, while HIF-1α inhibition significantly attenuated M2 polarization. These findings suggest hypoxia-mediated HIF-1α signaling may orchestrate macrophage phenotypic switching during oral carcinogenesis. CONCLUSIONS: During OLK malignant transformation, HIF-1α expression is progressively upregulated, driving the polarization shift of tissue macrophages from pro-inflammatory M1 to pro-tumorigenic M2 phenotypes.

Key words: Oral leukoplakia, Tumor-associated macrophages, Hypoxia-inducible factor-1α, Macrophage polarization, Hypoxic microenvironment

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