4.6 Article

Defining biomarkers in oral cancer according to smoking and drinking status

Journal

FRONTIERS IN ONCOLOGY
Volume 12, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fonc.2022.1068979

Keywords

oral cancer; prognostic biomarker; tumor microenvironment; oral squamous cell carcinoma; non-smoker; non-drinker

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This study found that smokers and drinkers have different immune profiles compared to non-smokers and non-drinkers in terms of cellular composition and cytokine expression in the tumor microenvironment, which may be useful for prognosis.
IntroductionOral Squamous Cell Carcinomas (OSCC) are mostly related to tobacco consumption eventually associated to alcohol (Smoker/Drinker patients: SD), but 25-30% of the patients have no identified risk factors (Non-Smoker/Non-Drinker patients: NSND). We hypothesized that these patients have distinguishable immune profiles that could be useful for prognosis. Materials and MethodsCells present in immune tumor microenvironment (TME) and blood from 87 OSCC HPV-negative patients were analyzed using a multiparameter flow cytometry assay, in a prospective case-control study. Cytokine levels in tumor supernatants and blood were determined by a cytometric bead array (CBA) assay. ResultsNormal gingiva and blood from healthy donors (HD) were used as controls. A significant increase of granulocytes (p<0.05 for blood), of monocytes-macrophages (p<0.01 for blood) and of CD4(+) T cells expressing CD45RO and CCR6 (p<0.001 for blood; p<0.0001 for TME) as well as higher levels of IL-6 (p<0.01 for sera, p<0.05 for tumor supernatant) were observed in SD patients as compared to NSND OSCC patients and HD. High percentages of CD4(+) T cells expressing CD45RO and CCR6 cells in tumor tissue (p=0.05) and blood (p=0.05) of SD OSCC patients were also associated with a poorer prognosis while a high percentage of regulatory T cells (Treg) in tumor tissue was associated with a more favorable prognostic factor (p=0.05). Also, a higher percentage of blood CD8(+) T lymphocytes among CD45(+) cells in NSND patients was associated with a better disease-free survival (p=0.004). ConclusionGranulocytes, monocytes-macrophages, and CD4(+) T cells expressing CD45RO and CCR6 in blood and TME as well as serum IL-6 can therefore distinguish OSCC SD and NSND patients. Quantifying the proportion of CD4(+) T cells expressing CD45RO and CCR6 and of Treg in SD patients and CD8(+) T cells in NSND patients could help defining the prognostic of OSCC patients.

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