Shi Yahong, Wang Wenjing, Bai Yunfang, Liu Xiaoying, Wu Liwei, Liu Ning
Department of Stomatology, Second Hospital of Shijiazhuang, Shijiazhuang, Hebei, 050000, PR China.
Department of Stomatology, The Fourth Hospital of Hebei Medical University, Shijiazhuang, Hebei, 050017, PR China.
Heliyon. 2024 Jul 24;10(15):e35131. doi: 10.1016/j.heliyon.2024.e35131. eCollection 2024 Aug 15.
This study investigated the impact of Human Papillomavirus (HPV) on inflammation and growth in oral epithelial cells, with a focus on the role of Interleukin-37 (IL37). Oral epithelial cells, including HOEC and HSC-3 cells, were employed in the research. The results revealed that HPV significantly induced inflammation in both types of oral epithelial cells, concurrently promoting cell growth and inhibiting apoptosis. IL37, a cytokine, was found to mitigate HPV-induced inflammation in oral epithelial cells. Moreover, IL37 counteracted HPV's effects on apoptosis and cell viability in oral epithelial cells. The study also identified a reduction in autophagy in HPV-infected oral epithelial cells, a phenomenon alleviated by IL37. Furthermore, chemical inhibition of autophagy was observed to attenuate HPV-induced inflammation and growth in oral epithelial cells. These findings contribute valuable insights into the pathogenesis of inflammation in oral epithelial cells associated with HPV and oral cancers, offering potential avenues for novel therapeutic strategies.
本研究调查了人乳头瘤病毒(HPV)对口腔上皮细胞炎症和生长的影响,重点关注白细胞介素-37(IL37)的作用。研究中使用了包括HOEC和HSC-3细胞在内的口腔上皮细胞。结果显示,HPV显著诱导了两种类型口腔上皮细胞的炎症,同时促进细胞生长并抑制细胞凋亡。细胞因子IL37被发现可减轻HPV诱导的口腔上皮细胞炎症。此外,IL37可抵消HPV对口腔上皮细胞凋亡和细胞活力的影响。该研究还发现HPV感染的口腔上皮细胞中自噬减少,而IL37可缓解这一现象。此外,观察到化学抑制自噬可减弱HPV诱导的口腔上皮细胞炎症和生长。这些发现为与HPV和口腔癌相关的口腔上皮细胞炎症发病机制提供了有价值的见解,为新的治疗策略提供了潜在途径。