AI Article Synopsis

  • Salivary gland adenoid cystic carcinoma (ACC), mucoepidermoid carcinoma (MEC), and oral squamous cell carcinoma (OSCC) are types of cancer in the head and neck, with previous treatments like immune checkpoint inhibitors failing in ACC.
  • The study investigated the effect of Gipie (CCDC88B), a protein that activates immune cells, by silencing it in cancer cell co-culture models and using various imaging and proteomic techniques.
  • Results showed that silencing Gipie in ACC cells led to increased cell death and activation of immune cells, suggesting that Gipie hinders anti-tumor immune responses in ACC but had little effect on other cancer types.

Article Abstract

Introduction: Salivary gland adenoid cystic carcinoma (ACC), mucoepidermoid carcinoma (MEC) and oral squamous cell carcinoma (OSCC) occurs within the head and neck region. So far immune check point inhibitors failed in ACC. Gipie (CCDC88B) is a microtubule linker protein that activates immune cells. Gipie expressions found in head and neck cancer cells. We hypothesised that the presence of Gipie diminishes anti-tumour reactivity of immune cells towards head and neck cancer.

Method: To determine the effect of Gipie in oral and salivary gland cancer cells, Gipie was silenced in cancer cells in cancer-immune cells co-culture models and we performed 3D Z series confocal imaging, annexin V and immune activation flow cytometry, proteome profiler and discovery phase proteomics.

Results: ACC cells morphed into pseudonormal morphology in immune co-culture models. Silencing Gipie in ACC cells showed significant increase of apoptotic cells and activated natural killer cells, and lowering of regulatory T cells. Other salivary and oral cancer cells showed negligible effect of Gipie. Proteome profiler and proteomics assay confirmed Gipie affecting proliferation mechanism and immune activated proteins in ACC immune co-culture models.

Conclusion: Overall, we conclude that the presence of Gipie has a confounding role during the ACC-immune cell interaction.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11425664PMC
http://dx.doi.org/10.1002/cnr2.70019DOI Listing

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