# Impaired intratumoral dendritic cell function and potential predictive value of dendritic cell markers for metastasis in malignant salivary gland tumors

**Authors:** Ana Guadalupe Gama-Cuellar, Katya Pulido Díaz, Mariana Martínez Calleja, Gabriela Anaya Saavedra, Velia Ramírez-Amador, Jorge Rodarte Corro, Victor Ramón-Ramírez, Ricardo Luiz Albuquerque-Júnior, Rogério Gondak

PMC · DOI: 10.4317/medoral.26248 · Medicina Oral, Patología Oral y Cirugía Bucal · 2023-11-22

## TL;DR

This study explores how immune cells called dendritic cells function in salivary gland tumors and how their markers might predict cancer spread.

## Contribution

The study identifies specific dendritic cell markers that may predict metastasis in malignant salivary gland tumors.

## Key findings

- Metastatic tumors showed lower intratumoral CD1a+ dendritic cells compared to non-metastatic tumors.
- HLA-DR+ and Ki-67+ cell densities differ significantly between benign and malignant salivary gland tumors.
- Dendritic cell markers may serve as predictive tools for metastasis in salivary gland malignancies.

## Abstract

The differentiation between primary and metastatic salivary gland neoplasms (SGNs) helps in determining appropriate management strategies, including the need for additional diagnostic tests, surveillance, or aggressive treatment. The purpose of this study was to identify and quantify the immature and mature dendritic cells (DCs) in metastatic and no metastatic SGNs and determine its association with clinicopathological findings.

Cross-sectional, observational, and descriptive study that includes 33 malignant salivary gland neoplasms [MSGN (6, 18.1% metastatic)], and 22 pleomorphic adenomas (PA), as a control group. Clinical and histopathological characteristics were obtained. Immunohistochemistry for human leukocyte antigen D-related (HLA-DR), CD1a, CD83, and Ki-67 proteins was done. Positive intra- and peritumoral DCs were counted.

Individuals with MSGN had a lower density of intratumoral HLA-DR+ cells than those with PA (p=0.001), Ki-67 immunostaining was significantly higher in MSGN than in PA (6% vs. 1.4%, p<0.001). Metastatic MSGN showed less intratumoral CD1a+ than non-metastatic (3.2 vs. 165.1, p=0.001). No differences in intra- and peritumoral CD83+ cells were found between benign and malignant SGN.

These results suggest that the immune-protective function of intratumoral DCs is compromised in MSGNs. DCs markers may represent useful prediction tools for metastases in salivary gland malignancies, with crucial implications in the implementation of appropriate disease management strategies.

## Linked entities

- **Proteins:** CD1A (CD1a molecule), CD83 (CD83 molecule), Mki67 (antigen identified by monoclonal antibody Ki 67)

## Full-text entities

- **Genes:** CD83 (CD83 molecule) [NCBI Gene 9308] {aka BL11, HB15}, CD1A (CD1a molecule) [NCBI Gene 909] {aka CD1, FCB6, HTA1, R4, T6}
- **Diseases:** Metastatic (MESH:D000092182), SGNs (MESH:D012468), PA (MESH:D008949), metastases (MESH:D009362)

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC10945878/full.md

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10945878/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC10945878/full.md

---
Source: https://tomesphere.com/paper/PMC10945878