Ha Na Hee, Woo Bok Hee, Kim Da Jeong, Ha Eun Sin, Choi Jeom Il, Kim Sung Jo, Park Bong Soo, Lee Ji Hye, Park Hae Ryoun
Department of Oral Pathology, School of Dentistry, Pusan National University, 49 Busandaehak-Ro, Yangsan-Si, Kyeongsangnam-Do, 626-870, South Korea.
Department of Periodontology, School of Dentistry, Pusan National University, 49 Busandaehak-Ro, Yangsan, 626-870, South Korea.
Tumour Biol. 2015 Dec;36(12):9947-60. doi: 10.1007/s13277-015-3764-9. Epub 2015 Jul 16.
Periodontitis is the most common chronic inflammatory condition occurring in the human oral cavity, but our knowledge on its contribution to oral cancer is rather limited. To define crosstalk between chronic periodontitis and oral cancer, we investigated whether Porphyromonas gingivalis, a major pathogen of chronic periodontitis, plays a role in oral cancer progression. To mimic chronic irritation by P. gingivalis in the oral cavity, oral squamous cell carcinoma (OSCC) cells were infected with P. gingivalis twice a week for 5 weeks. Repeated infection of oral cancer cells by P. gingivalis resulted in morphological changes of host cancer cells into an elongated shape, along with the decreased expression of epithelial cell markers, suggesting acquisition of an epithelial-to-mesenchymal transition (EMT) phenotype. The prolonged exposure to P. gingivalis also promoted migratory and invasive properties of OSCC cells and provided resistance against a chemotherapeutic agent, all of which are described as cellular characteristics undergoing EMT. Importantly, long-term infection by P. gingivalis induced an increase in the expression level of CD44 and CD133, well-known cancer stem cell markers, and promoted the tumorigenic properties of infected cancer cells compared to non-infected controls. Furthermore, increased invasiveness of P. gingivalis-infected OSCC cells was correlated with enhanced production of matrix metalloproteinase (MMP)-1 and MMP-10 that was stimulated by interleukin-8 (IL-8) release. This is the first report demonstrating that P. gingivalis can increase the aggressiveness of oral cancer cells via epithelial-mesenchymal transition-like changes and the acquisition of stemness, implicating P. gingivalis as a potential bacterial risk modifier.
牙周炎是人类口腔中最常见的慢性炎症性疾病,但我们对其在口腔癌发生中的作用了解相当有限。为了明确慢性牙周炎与口腔癌之间的相互作用,我们研究了慢性牙周炎的主要病原体牙龈卟啉单胞菌是否在口腔癌进展中发挥作用。为模拟牙龈卟啉单胞菌在口腔中的慢性刺激,每周两次用牙龈卟啉单胞菌感染口腔鳞状细胞癌(OSCC)细胞,持续5周。牙龈卟啉单胞菌反复感染口腔癌细胞导致宿主癌细胞形态变为细长形,同时上皮细胞标志物表达降低,提示获得了上皮-间质转化(EMT)表型。长期暴露于牙龈卟啉单胞菌还促进了OSCC细胞的迁移和侵袭特性,并使其对化疗药物产生耐药性,所有这些都被描述为发生EMT的细胞特征。重要的是,与未感染的对照组相比,牙龈卟啉单胞菌的长期感染导致著名的癌症干细胞标志物CD44和CD133表达水平升高,并促进了感染癌细胞的致瘤特性。此外,牙龈卟啉单胞菌感染的OSCC细胞侵袭性增加与白细胞介素-8(IL-8)释放刺激的基质金属蛋白酶(MMP)-1和MMP-10产生增加相关。这是首次报道表明牙龈卟啉单胞菌可通过上皮-间质转化样变化和干性获得增加口腔癌细胞的侵袭性,提示牙龈卟啉单胞菌是一种潜在的细菌风险调节因子。