R. Chakraborty, Honghua Hu, A. Mangani, K. Vickery, S. Ranganathan
{"title":"联合细菌抗原脂多糖和脂壁酸促进口腔癌细胞增殖","authors":"R. Chakraborty, Honghua Hu, A. Mangani, K. Vickery, S. Ranganathan","doi":"10.31487/J.DOBCR.2021.01.03","DOIUrl":null,"url":null,"abstract":"Oral biofilms harbour gram-negative bacterial antigen lipopolysaccharide (LPS) involved in oral cancer\nprogression and gram-positive bacterial surface-associated adhesive, lipoteichoic acid (LTA). Thus, we\nhypothesised that LPS and LTA together would increase the proliferation of cancer cells compared to\nstimulation by LPS alone. Oral cancer cell lines SCC4, SCC9, SCC25, Cal 27 and the normal oral cell line,\nOKF6, were studied. The bacterial antigen stimulation indices were determined using the MT Glo assay.\nCell proliferation after bacterial antigen stimulation was validated by clonogenic assays. Phosphokinase\narray, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and Western blot were\nemployed to study proliferative and apoptotic pathways in bacterial antigen-stimulated cells. Bacterial\nantigens significantly stimulated Cal 27 (p ≤ 0.001) alone. SCC4 and SCC9 showed negligible stimulation\nwith either antigen, while SCC25 results were comparable to OKF6. The combined antigen stimulation of\nCal 27 led to a decrease in phosphorylated p53 and β-catenin and higher PI3K compared to LPS only\nstimulated cells (p ≤ 0.001). Combined bacterial antigen stimulation results in increased proliferation of Cal\n27 cells due to lowering of tumor suppressor proteins and increased tumor proliferation-related proteins.","PeriodicalId":72781,"journal":{"name":"Dental Oral Biology and Craniofacial Research","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"4","resultStr":"{\"title\":\"Combined Bacterial Antigen Lipopolysaccharide and Lipoteichoic Acid Increase Cal 27 Oral Cancer Cell Proliferation\",\"authors\":\"R. Chakraborty, Honghua Hu, A. Mangani, K. Vickery, S. Ranganathan\",\"doi\":\"10.31487/J.DOBCR.2021.01.03\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Oral biofilms harbour gram-negative bacterial antigen lipopolysaccharide (LPS) involved in oral cancer\\nprogression and gram-positive bacterial surface-associated adhesive, lipoteichoic acid (LTA). Thus, we\\nhypothesised that LPS and LTA together would increase the proliferation of cancer cells compared to\\nstimulation by LPS alone. Oral cancer cell lines SCC4, SCC9, SCC25, Cal 27 and the normal oral cell line,\\nOKF6, were studied. The bacterial antigen stimulation indices were determined using the MT Glo assay.\\nCell proliferation after bacterial antigen stimulation was validated by clonogenic assays. Phosphokinase\\narray, reverse transcription-quantitative polymerase chain reaction (RT-qPCR), and Western blot were\\nemployed to study proliferative and apoptotic pathways in bacterial antigen-stimulated cells. Bacterial\\nantigens significantly stimulated Cal 27 (p ≤ 0.001) alone. SCC4 and SCC9 showed negligible stimulation\\nwith either antigen, while SCC25 results were comparable to OKF6. The combined antigen stimulation of\\nCal 27 led to a decrease in phosphorylated p53 and β-catenin and higher PI3K compared to LPS only\\nstimulated cells (p ≤ 0.001). Combined bacterial antigen stimulation results in increased proliferation of Cal\\n27 cells due to lowering of tumor suppressor proteins and increased tumor proliferation-related proteins.\",\"PeriodicalId\":72781,\"journal\":{\"name\":\"Dental Oral Biology and Craniofacial Research\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-02-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"4\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Dental Oral Biology and Craniofacial Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31487/J.DOBCR.2021.01.03\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Dental Oral Biology and Craniofacial Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/J.DOBCR.2021.01.03","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
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.