Combined bacterial antigen lipopolysaccharide and lipoteichoic acid increase Cal 27 oral cancer cell proliferation

Rajdeep Chakraborty, Honghua Hu, Abubakar Siddiq Mangani, Karen Vickery, Shoba Ranganathan*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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Abstract

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.
Original languageEnglish
Pages (from-to)1-6
Number of pages6
JournalDental Oral Biology and Craniofacial Research
Volume4
Issue number1
DOIs
Publication statusPublished - 8 Feb 2021

Bibliographical note

Copyright the Author(s) 2021. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.

Keywords

  • Bacterial antigen
  • LPS
  • LTA
  • biofilm
  • oral cancer cell
  • proliferation
  • phosphokinase

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