# Synergistic drug combination screening using a nanodroplet processing platform to enhance neuroblastoma treatment in TH‐MYCN transgenic mice

**Authors:** Yen‐Tzu Liao, Zhi‐Kai Yu, Yi‐Xun Huang, Kuan‐Hung Lin, Ching‐Te Kuo, Tsai‐Shan Yang, Pei‐Yi Wu, Chi‐Tai Yeh, Yen‐Lin Liu, Chien‐Chin Chen, Chiung‐Nien Chen, Wen‐Ming Hsu, Hsinyu Lee

PMC · DOI: 10.1002/btm2.70007 · 2025-03-03

## TL;DR

A new nanodroplet platform screens drug combinations for neuroblastoma, showing effective and less toxic treatments in mice.

## Contribution

The BioNDP platform enables efficient, low-cell drug screening with high translational potential for personalized neuroblastoma therapy.

## Key findings

- A synergistic drug combination eradicated tumors in TH-MYCN mice.
- The treatment improved survival rates without significant side effects.
- The BioNDP platform uses 100 cells and 200 nL per well for drug screening.

## Abstract

Neuroblastoma is a highly aggressive pediatric cancer with a poor prognosis, particularly in high‐risk (HR) cases characterized by MYCN amplification. The severe side effects associated with high‐dose chemotherapy further complicate treatment. Despite significant advancements in drug screening, traditional platforms remain limited due to their requirement for large cell quantities and their low translational success from bench to clinic. These limitations hinder the application of personalized medicine screening for patients with neuroblastoma. To address these challenges, we developed a Bioinspired Nanodroplet Processing (BioNDP) platform. This innovative platform allows for the simultaneous screening of multiple drug combinations while reducing the required number of cells to just 100 and minimizing assay volumes to 200 nL per well. Using BioNDP, we screened chemotherapeutic combinations of cyclophosphamide, doxorubicin, and vincristine in both the SK‐N‐DZ neuroblastoma cell line and primary neuroblastoma cells derived from TH‐MYCN transgenic mice. Our findings revealed a specific drug combination that exhibited significant synergistic cytotoxicity in neuroblastoma cells. This combination completely eradicated tumors and significantly improved survival rates in TH‐MYCN mice, without notable side effects. This study highlights the potential of the BioNDP platform in bridging in vitro and in vivo results, offering a promising strategy for personalized medicine in the treatment of HR neuroblastoma, with reduced toxicity and enhanced therapeutic efficacy.

## Linked entities

- **Genes:** MYCN (MYCN proto-oncogene, bHLH transcription factor) [NCBI Gene 4613]
- **Chemicals:** cyclophosphamide (PubChem CID 2907), doxorubicin (PubChem CID 31703), vincristine (PubChem CID 5978)
- **Diseases:** neuroblastoma (MONDO:0005072)
- **Species:** Mus musculus (taxon 10090)

## Full-text entities

- **Genes:** Mycn (Mycn proto-oncogene, bHLH transcription factor) [NCBI Gene 18109] {aka N-myc, Nmyc, Nmyc-1, Nmyc1, bHLHe37, c-nmyc}, Th (tyrosine hydroxylase) [NCBI Gene 21823]
- **Diseases:** pediatric cancer (MESH:D009369), cytotoxicity (MESH:D064420), Neuroblastoma (MESH:D009447)
- **Chemicals:** doxorubicin (MESH:D004317), vincristine (MESH:D014750), cyclophosphamide (MESH:D003520)
- **Species:** Mus musculus (house mouse, species) [taxon 10090], Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** SK-N-DZ — Homo sapiens (Human), Neuroblastoma, Cancer cell line (CVCL_1701)

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12284426/full.md

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Source: https://tomesphere.com/paper/PMC12284426