Evidence map›Paper›PMID 40708972›Full record

ArticleBioengineering & translational medicine2025

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

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 and 3 more

Abstract read
In one paragraph

Article in Bioengineering & translational medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors.

Yen-Tzu LiaoDepartment of Life Science National Taiwan University Taipei City Taiwan.
Zhi-Kai YuDepartment of Life Science National Taiwan University Taipei City Taiwan.
Yi-Xun HuangDepartment of Life Science National Taiwan University Taipei City Taiwan.
Kuan-Hung LinDepartment of Life Science National Taiwan University Taipei City Taiwan.
Ching-Te KuoDepartment of Mechanical and Electro-Mechanical Engineering National Sun Yat-sen University Kaohsiung City Taiwan.
Tsai-Shan YangDivision of Pediatric Surgery, Department of Surgery National Taiwan University Hospital Taipei City Taiwan.
Pei-Yi WuDepartment of Life Science National Central University Taoyuan City Taiwan.
Chi-Tai YehDepartment of Pediatrics, School of Medicine, College of Medicine Taipei Medical University Taipei City Taiwan.
Yen-Lin LiuDepartment of Pediatrics, School of Medicine, College of Medicine Taipei Medical University Taipei City Taiwan.
Chien-Chin ChenDepartment of Pathology Ditmanson Medical Foundation Chia-Yi Christian Hospital Chiayi Taiwan.
Chiung-Nien ChenDepartment of Surgery National Taiwan University Hospital Taipei City Taiwan.
Wen-Ming HsuDivision of Pediatric Surgery, Department of Surgery National Taiwan University Hospital Taipei City Taiwan.
Hsinyu LeeDepartment of Life Science National Taiwan University Taipei City Taiwan.ORCID https://orcid.org/0000-0002-1477-0183

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

BioNDPchemotherapydrug screeningneuroblastomasynergyTH‐MYCN mice

Identifiers

PMID40708972
PMCPMC12284426

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.