# Immunological Analysis of Oral Cytobrush Specimens for Early Detection of Oral Cancer Biomarkers: A Comprehensive Review

**Authors:** Reem Hanna, Alberto Luigi Rebaudi, Saman Warnakulasuriya, Senada Koljenovic, Maria Menini, Francesco Laganà, Bernardo Bianchi, Paolo Iacoviello, Mauro Labanca, Marco Greppi, Federico Rebaudi, Silvia Pesce, Alberto Rebaudi, Emanuela Marcenaro

PMC · DOI: 10.3390/ijms27042059 · International Journal of Molecular Sciences · 2026-02-23

## TL;DR

This review explores how oral cytobrush samples can detect early signs of oral cancer through immunological biomarkers, offering a non-invasive alternative to traditional methods.

## Contribution

The paper introduces the use of oral cytobrush specimens for immunological profiling as a novel, minimally invasive method for early oral cancer detection.

## Key findings

- Oral cytobrush specimens can detect biomarkers like p53, Ki-67, and IL-6 linked to early oral carcinogenesis.
- OCB-based immunoanalysis correlates with epithelial dysplasia and non-invasive neoplastic transformation.
- OCB sampling is a reliable and patient-friendly method for immunological and molecular analyses.

## Abstract

Early identification of the risk of malignant transformation in oral potentially malignant disorders (OPMDs) is critical for improving outcomes in oral squamous cell carcinoma (OSCC). This comprehensive review examines immunological biomarkers obtained from minimally invasive oral cytobrush (OCB) specimens for the early detection of OSCC within a precision medicine framework. The objectives were to (1) identify and characterise key immunological biomarkers associated with early oral carcinogenesis; (2) evaluate the diagnostic utility of OCB sampling for detecting these biomarkers; and (3) explore the potential of OCB-based profiling to support personalised screening and patient management. The review highlights the potential advantages of OCB compared with conventional diagnostic methods, as reported in the literature, particularly its ability to capture early malignant changes through immunological analysis. Evidence is discussed for biomarker pathways related to cell-cycle and differentiation dysregulation (p53, Ki-67, CKs), inflammation-driven epithelial transformation (IL-1β, IL-6, IL-8, TNF-α), and immune suppression and checkpoint activation (PD-L1, B7-H6). OCB provides reliable and patient-friendly cyto-salivary samples that are suitable for immunological and molecular analyses. Aberrant biomarker expression detected in OCB specimens correlates with epithelial dysplasia and reflects early non-invasive neoplastic transformation, supporting the diagnostic value of integrated biomarker panels. Overall, OCB-based immunoanalysis represents a practical, non-invasive approach for the early detection of OSCC. Emerging technologies, including AI and multi-omics approaches, may further support the precision and predictive values of immunological analysis for OSCC. When combined with relevant biomarker pathways reflecting tumour biology and host immune responses, this strategy could offer a strong foundation for precision-medicine screening. It may also support personalised monitoring in patients with OPMDs.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157], Mki67 (antigen identified by monoclonal antibody Ki 67) [NCBI Gene 17345], CKS (Nucleotide-diphospho-sugar transferases superfamily protein) [NCBI Gene 841733], IL1B (interleukin 1 beta) [NCBI Gene 3553], IL6 (interleukin 6) [NCBI Gene 3569], CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576], TNF (tumor necrosis factor) [NCBI Gene 7124], CD274 (CD274 molecule) [NCBI Gene 29126], NCR3LG1 (natural killer cell cytotoxicity receptor 3 ligand 1) [NCBI Gene 374383]
- **Diseases:** oral squamous cell carcinoma (MONDO:0004958)

## Full-text entities

- **Genes:** KRT19 (keratin 19) [NCBI Gene 3880] {aka CK19, K19, K1CS}, KRT18 (keratin 18) [NCBI Gene 3875] {aka CK-18, CYK18, K18}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, KRT8 (keratin 8) [NCBI Gene 3856] {aka CARD2, CK-8, CK8, CYK8, K2C8, K8}, KRT13 (keratin 13) [NCBI Gene 3860] {aka CK13, K13, WSN2}, FMOD (fibromodulin) [NCBI Gene 2331] {aka FM, SLRR2E}, BCL2 (BCL2 apoptosis regulator) [NCBI Gene 596] {aka Bcl-2, PPP1R50}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, STAT3 (signal transducer and activator of transcription 3) [NCBI Gene 6774] {aka ADMIO, ADMIO1, APRF, HIES}, NCR3LG1 (natural killer cell cytotoxicity receptor 3 ligand 1) [NCBI Gene 374383] {aka B7-H6, B7H6, DKFZp686O24166}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, NCR3 (natural cytotoxicity triggering receptor 3) [NCBI Gene 259197] {aka 1C7, CD337, LY117, MALS, NKp30}, HLA-E (major histocompatibility complex, class I, E) [NCBI Gene 3133] {aka HLA-6.2, QA1}, KRT17 (keratin 17) [NCBI Gene 3872] {aka 39.1, CK-17, K17, PC2, PCHC1}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}, TXK (TXK tyrosine kinase) [NCBI Gene 7294] {aka BTKL, PSCTK5, PTK4, RLK, TKL}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, CXCL8 (C-X-C motif chemokine ligand 8) [NCBI Gene 3576] {aka GCP-1, GCP1, IL8, LECT, LUCT, LYNAP}, PIK3CB (phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) [NCBI Gene 5291] {aka P110BETA, PI3K, PI3KBETA, PIK3C1}
- **Diseases:** HNC (MESH:D006258), anxiety (MESH:D001007), oral epithelial lesions (MESH:D017573), Cancer (MESH:D009369), OLP (MESH:D017676), precancerous (MESH:D011230), cervical cancer (MESH:D002583), pain (MESH:D010146), oral abnormalities (MESH:D009056), dysplasia (MESH:D015792), OLP lesions (MESH:D008010), Chronic inflammation (MESH:D007249), Micrometastasis (MESH:D061206), injury to (MESH:D014947), metastasis (MESH:D009362), OSCC (MESH:D000077195), dysplastic (MESH:D004416), chronic (MESH:D002908), OPMD (MESH:C537245), HPV infection (MESH:D030361), necrotic (MESH:D009336), tongue lesions (MESH:D014060), PVL (MESH:D007971), carcinogenesis (MESH:D063646), OCB (MESH:D020820), OC (MESH:D009062), traumatic fibroma (MESH:D005350), lymph-node metastasis (MESH:D008207), epithelial dysplasia (MESH:C567703), autoimmune or dermatological diseases (MESH:D001327), OPMD lesion (MESH:D009059)
- **Chemicals:** Cytobrush (-), chlorhexidine (MESH:D002710), alcohol (MESH:D000438), water (MESH:D014867), ATP (MESH:D000255)
- **Species:** Homo sapiens (human, species) [taxon 9606], Nicotiana tabacum (American tobacco, species) [taxon 4097]
- **Cell lines:** OCB — Homo sapiens (Human), Buccal mucosa squamous cell carcinoma, Cancer cell line (CVCL_D859)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12940661/full.md

## References

95 references — full list in the complete paper: https://tomesphere.com/paper/PMC12940661/full.md

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Source: https://tomesphere.com/paper/PMC12940661