STAT3 interactome predicts presence of proteins that regulate immune system in oral squamous cell carcinoma

Rajdeep Chakraborty*, Pallavi Khodlan, Aidan Tay, Fei Liu

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

1 Citation (Scopus)

Abstract

Objectives: Signal transducer and activator of transcription 3 (STAT3) is one of the key proliferation mechanism–related proteins that helps in oral squamous cell carcinoma (OSCC) progression. Immune evasion by STAT3 is mediated by the JAK2/STAT3/PDL1 signaling axis. Based on previous findings, we hypothesized that STAT3-binding partners participate in the inhibition of anti-tumor activity in OSCC.

Methods: A 3D cancer-immune co-culture model was constructed using oral cancer cell lines SCC4, SCC9, SCC25, and CAL27 and normal oral cell line OKF6. The cells were co-cultured with natural killer (NK-92) and Jurkat cells. The target protein STAT3 was chosen based on SWATH data, and co-immunoprecipitation (Co-IP)-based proteomics was conducted. The Co-IP LC-MS/MS output was analysed to determine the protein interaction network, gene ontology, pathway analysis, and protein cluster annotation.

Results: STAT3 in oral cancer cell lines interacts with the epidermal growth factor receptor (EGFR) and other proteins that participate in proliferation and immune mechanisms. Proteome analysis showed that some STAT3-binding proteins found in this study are known immune system regulators.

Conclusion: Overall, STAT3 interactive proteins regulate the immune system in oral squamous cell carcinoma cells.
Original languageEnglish
Number of pages7
JournalJournal of Oral Biosciences
Early online date3 Sept 2024
DOIs
Publication statusE-pub ahead of print - 3 Sept 2024

Bibliographical note

Copyright the Author(s) 2024. 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

  • STAT3
  • Oral cancer
  • Protein-protein interaction
  • Anti-tumour reactivity
  • Proteomics

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