联合细菌抗原脂多糖和脂壁酸促进口腔癌细胞增殖

R. Chakraborty, Honghua Hu, A. Mangani, K. Vickery, S. Ranganathan
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引用次数: 4

摘要

口腔生物膜含有参与口腔癌进展的革兰氏阴性细菌抗原脂多糖(LPS)和革兰氏阳性细菌表面相关粘合剂脂磷壁酸(LTA)。因此,我们假设与单独用LPS刺激相比,LPS和LTA一起会增加癌症细胞的增殖。对癌症口腔细胞株SCC4、SCC9、SCC25、Cal 27和正常口腔细胞株OKF6进行了研究。使用MT-Glo测定法测定细菌抗原刺激指数。细菌抗原刺激后的细胞增殖通过克隆形成试验得到验证。采用磷酸激酶阵列、逆转录定量聚合酶链式反应(RT-qPCR)和蛋白质印迹研究细菌抗原刺激细胞的增殖和凋亡途径。细菌抗原单独显著刺激Cal 27(p≤0.001)。SCC4和SCC9对任一抗原的刺激可忽略不计,而SCC25的结果与OKF6相当。与仅LPS刺激的细胞相比,联合抗原刺激Cal27导致磷酸化p53和β-连环蛋白降低,PI3K升高(p≤0.001)。联合细菌抗原刺激导致Cal27细胞增殖增加,这是由于肿瘤抑制蛋白降低和肿瘤增殖相关蛋白增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Combined Bacterial Antigen Lipopolysaccharide and Lipoteichoic Acid Increase Cal 27 Oral Cancer Cell Proliferation
Oral biofilms harbour gram-negative bacterial antigen lipopolysaccharide (LPS) involved in oral cancer progression and gram-positive bacterial surface-associated adhesive, lipoteichoic acid (LTA). Thus, we hypothesised that LPS and LTA together would increase the proliferation of cancer cells compared to stimulation by LPS alone. Oral cancer cell lines SCC4, SCC9, SCC25, Cal 27 and the normal oral cell line, OKF6, were studied. The bacterial antigen stimulation indices were determined using the MT Glo assay. Cell proliferation after bacterial antigen stimulation was validated by clonogenic assays. Phosphokinase array, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and Western blot were employed to study proliferative and apoptotic pathways in bacterial antigen-stimulated cells. Bacterial antigens significantly stimulated Cal 27 (p ≤ 0.001) alone. SCC4 and SCC9 showed negligible stimulation with either antigen, while SCC25 results were comparable to OKF6. The combined antigen stimulation of Cal 27 led to a decrease in phosphorylated p53 and β-catenin and higher PI3K compared to LPS only stimulated cells (p ≤ 0.001). Combined bacterial antigen stimulation results in increased proliferation of Cal 27 cells due to lowering of tumor suppressor proteins and increased tumor proliferation-related proteins.
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