Porphyromonas gingivalis increases the invasiveness of oral cancer cells by upregulating IL-8 and MMPs

牙龈卟啉单胞菌 慢性牙周炎 基质金属蛋白酶 牙周病原体 下调和上调 牙周炎 炎症 癌症 免疫学 癌症研究 细胞因子 癌细胞 分泌物 医学 生物 内科学 生物化学 基因
作者
Na Hee Ha,Dae Gun Park,Bok Hee Woo,Da Jeong Kim,Jeom‐Il Choi,Bong-Soo Park,Yong Deok Kim,Jihye Lee,Hae Ryoun Park
出处
期刊:Cytokine [Elsevier BV]
卷期号:86: 64-72 被引量:96
标识
DOI:10.1016/j.cyto.2016.07.013
摘要

Recent studies indicate that chronic inflammation promotes the aggressiveness of cancers. However, the direct molecular mechanisms underlying a functional link between chronic periodontitis, the most common form of oral inflammatory diseases, and the malignancy of oral cancer remain unknown. To elucidate the role of chronic periodontitis in progression of oral cancer, we examined the effect of Porphyromonas gingivalis (P. gingivalis), a major pathogen that causes chronic periodontitis, on the invasiveness of oral squamous cell carcinoma (OSCC) cells, including SCC-25, OSC-20 and SAS cells. Exposures to P. gingivalis promoted the invasive ability of OSC-20 and SAS cells via the upregulation of matrix metalloproteinases (MMPs), specifically MMP-1 and MMP-2. However, P. gingivalis-infected SCC-25 cells did not exhibit changes in their invasive properties or the low expression levels of MMPs. In an effort to delineate the molecular players that control the invasiveness, we first assessed the level of interleukin-8 (IL-8), a well-known inflammatory cytokine, in P. gingivalis-infected OSCC cells. IL-8 secretion was substantially increased in the OSC-20 and SAS cells, but not in the SCC-25 cells, following P. gingivalis infection. When IL-8 was directly applied to SCC-25 cells, their invasive ability and MMP level were significantly increased. Furthermore, the downregulation of IL-8 in P. gingivalis-infected OSC-20 and SAS cells attenuated their invasive potentials and MMP levels. Taken together, our findings strongly suggest that P. gingivalis infection plays an important role in the promotion of the invasive potential of OSCC cells via the upregulation of IL-8 and MMPs.
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