# Assessment of the Circulating PD-1 and PD-L1 Levels and P53 Expression as a Predictor of Relapse in Pediatric Patients with Wilms Tumor and Hypernephroma

**Authors:** Heba A. Sahyon, Nadaa S. Alharbi, Zummar Asad, Mohamed A. El Shishtawy, Safaa A. Derbala

PMC · DOI: 10.3390/children11091035 · 2024-08-23

## TL;DR

This study explores how levels of PD-1, PD-L1, and P53 in blood can predict relapse in children with Wilms tumor and hypernephroma.

## Contribution

The study introduces a non-invasive method using circulating PD-L1 and P53 levels to predict relapse in pediatric renal tumors.

## Key findings

- Relapsed patients showed increased circulating PD-L1 levels before and after chemotherapy.
- P53 expression significantly decreased after one year of chemotherapy in relapsed patients.
- Circulating PD-L1 can serve as a reliable predictor of tumor relapse.

## Abstract

Background/Objectives: Wilms tumor (WT) is the most common form of pediatric renal tumor, accounting for over 90% of cases followed by hypernephroma. Some pediatric patients with WT (10%) experience relapse or metastasis and have poor survival rates. PD-L1 assists cancer cells in escaping damage from the immune system. P53 mutations are found in relapsed WT tumor samples. We hypothesized that testing circulating PD-1 and PD-L1 and P53 expression levels could offer a simple method to predict patient relapse and explore novel treatments for pediatric WTs and hypernephroma. Methods: Flow cytometric detection of cPD-1, cPD-L1, and P53 expression in relapsed and in-remission WT and hypernephroma before and after one year of chemotherapy was performed. Results: Our data shows increased levels of cPD-L1 in relapsed pediatric patients with WT or hypernephroma before and after chemotherapy. There were also slight and significant increases in cPD-1 levels in relapsed groups before chemotherapy. Additionally, we observed significant decreases in P53 expression after one year of chemotherapy in relapsed pediatric patients. Conclusions: Our study found that circulating PD-L1 can be used as a predictor marker for WT and hypernephroma relapse. In conclusion, these circulating markers can assist in monitoring relapse in WT and hypernephroma patients without the need for several biopsies.

## Linked entities

- **Genes:** TP53 (tumor protein p53) [NCBI Gene 7157]
- **Proteins:** PDCD1 (programmed cell death 1), CD274 (CD274 molecule)
- **Diseases:** Wilms tumor (MONDO:0006058), hypernephroma (MONDO:0005005)

## Full-text entities

- **Genes:** CLA3 (cerebellar ataxia 3 (cerebellar parenchyma disorder 1)) [NCBI Gene 1167] {aka CPD1, SCAR6}, CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, PDCD1 (programmed cell death 1) [NCBI Gene 5133] {aka ADMIO4, AIMTBS, CD279, PD-1, PD1, SLEB2}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}
- **Diseases:** Hypernephroma (MESH:D002292), metastasis (MESH:D009362), pediatric renal tumor (MESH:D007680), cancer (MESH:D009369), WT (MESH:D009396)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11430274/full.md

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Source: https://tomesphere.com/paper/PMC11430274