Lança Maria Leticia de Almeida, Conceição Nathan Steven Cezar da, Malta Isabella Souza, Meneses Daniela Oliveira, Almeida Luciana Yamamoto, Kaminagakura Estela
Department of Bioscience and Oral Diagnosis, Institute of Science and Technology, University of São Paulo State, Avenue Engenheiro Francisco José Longo, 777, São José dos Campos, São Paulo 12245-000, Brazil.
Int J Mol Sci. 2025 Aug 22;26(17):8120. doi: 10.3390/ijms26178120.
Oral leukoplakia (OL) is the most common potentially malignant oral disorder, with variable risk of progression to oral squamous cell carcinoma (OSCC). This study evaluated the chemopreventive and immunomodulatory potential of Artemisinin (ART) and (RO), alone or combined (ARO), in a 4NQO-induced murine model. Mice received 4NQO (100 µg/mL) in drinking water, and treatments began at week 8. Animals were euthanized at weeks 12 and 16 for histological, apoptotic (caspases-3, -8, -9; calreticulin), inflammatory (IL-1β, IL-10, HMGB1), and immune (CD8, CD68, CD56, IFN-γ, GM-CSF) marker analyses. RO-treated animals showed delayed malignant transformation, with no carcinomas at week 16 and increased expression of caspase-9, calreticulin, HMGB1, IFN-γ, and GM-CSF, indicating transient activation of antitumor immune responses. ART-treated mice showed increased CD68 and reduced CD56 expression, suggesting an immunosuppressive profile and higher carcinoma incidence. The ARO combination did not improve outcomes beyond ART alone. These findings support the immunomodulatory and pro-apoptotic effects of RO in delaying OL progression, highlighting its chemopreventive potential. ART showed limited benefit under current conditions, warranting further investigation into dose optimization and synergistic strategies.
口腔白斑(OL)是最常见的潜在恶性口腔疾病,发展为口腔鳞状细胞癌(OSCC)的风险各异。本研究在4NQO诱导的小鼠模型中评估了青蒿素(ART)和雷琐辛(RO)单独或联合使用(ARO)的化学预防和免疫调节潜力。小鼠饮用含4NQO(100 µg/mL)的水,治疗在第8周开始。在第12周和第16周对动物实施安乐死,进行组织学、凋亡(半胱天冬酶-3、-8、-9;钙网蛋白)、炎症(IL-1β、IL-10、HMGB1)和免疫(CD8、CD68、CD56、IFN-γ、GM-CSF)标志物分析。RO治疗的动物恶性转化延迟,在第16周无癌发生,且半胱天冬酶-9、钙网蛋白、HMGB1、IFN-γ和GM-CSF的表达增加,表明抗肿瘤免疫反应短暂激活。ART治疗的小鼠CD68表达增加而CD56表达降低,提示具有免疫抑制特征且癌发病率更高。ARO联合使用并未比单独使用ART改善更多结局。这些发现支持RO在延缓OL进展方面的免疫调节和促凋亡作用,突出了其化学预防潜力。在当前条件下,ART显示出有限的益处,需要进一步研究剂量优化和协同策略。