Evidence map›Paper›PMID 40052411›Full record

ArticleCancer science2025

ATR Inhibition Synergizes With Alkylating PI Polyamide Targeting MYCN by Suppressing DNA Repair in MYCN-Amplified Neuroblastoma.

Xiaoyi Lai, Hiroyuki Yoda, Yuming Qiao, Yuki Kida, Keizo Takenaga, Yoshinao Shinozaki, Nobuko Koshikawa, Atsushi Takatori

Abstract read
In one paragraph

Article in Cancer science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Targeted therapies in pediatric oncology: A start.Molecular therapy. Oncology · 2026
    Review
  3. Article
  4. 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

8 authors.

Xiaoyi LaiDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.
Hiroyuki YodaDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.ORCID https://orcid.org/0000-0002-5528-8940
Yuming QiaoDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.
Yuki KidaDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.
Keizo TakenagaDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.ORCID https://orcid.org/0000-0002-5341-6742
Yoshinao ShinozakiDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.
Nobuko KoshikawaDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.
Atsushi TakatoriDivision of Innovative Cancer Therapeutics, Chiba Cancer Center Research Institute, Chiba, Japan.ORCID https://orcid.org/0000-0002-2184-6721

Funding

AMED JP22ek0210168Japan Agency for Medical Research and Development (AMED)-Moonshot JP22zf0127001Japan Agency for Medical Research and Development (AMED)-Moonshot JP23zf0127001JSPS KAKENHI JP22H04923JSPS KAKENHI JP22K07245JST SPRING JPMJSP2109Takeda Science Foundation
6 · The paper itself

Abstract

Amplification of MYCN is a major oncogenic driver of high-risk neuroblastomas. We previously developed CCC-002, a MYCN-selective pyrrole-imidazole polyamide conjugated to a DNA alkylating agent. Administration of CCC-002 to MYCN-amplified (MYCN-amp) neuroblastoma cells triggered the activation of DNA damage responses. Here, we demonstrated that among the DNA damage response inhibitors, ataxia telangiectasia and Rad3-related (ATR) inhibitors synergized with CCC-002 to suppress DNA repair-related genes and induce apoptosis in MYCN-amp neuroblastoma cells. A synergistic antitumor effect was verified in an SK-N-BE(2) xenograft mouse model, in which the combined use of CCC-002 and ATR inhibitor at low doses significantly inhibited tumor progression. Notably, SK-N-BE(2) and SK-N-DZ cells, which showed ATM activation after CCC-002 treatment, exhibited high sensitivity to the combined treatment of ATR inhibitors. Comprehensive analysis of the gene expression profiles revealed that the combination treatment upregulated apoptosis-related pathways and downregulated DNA repair-related pathways. After the combined treatment of CCC-002 and ATR inhibitor, MYCN-amp cells showed less FISH probe signal and mRNA expression of MYCN, which was accompanied by an increase in DNA damage markers in the genomic region of MYCN, highlighting that ATR inhibitors synergize with CCC-002 and play a crucial role in the development of a novel MYCN-targeting therapy for MYCN-amp neuroblastoma.

Indexed as

Ataxia Telangiectasia Mutated ProteinsDNA RepairNeuroblastomaN-Myc Proto-Oncogene ProteinNylonsAnimalsApoptosisCell Line, TumorDNA DamageDrug SynergismGene AmplificationGene Expression Regulation, NeoplasticHumansImidazolesMicePyrrolesAtaxia Telangiectasia Mutated ProteinsATR protein, humanImidazolesMYCN protein, humanN-Myc Proto-Oncogene ProteinNylonsPyrrolesATR inhibitioncombined treatmentDNA damageMYCN‐amp neuroblastomaPI polyamide

Identifiers

PMID40052411
PMCPMC12127093

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Registered trials

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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.