Evidence map›Paper›PMID 40032551›Full record

ArticleJournal of medicinal chemistry2025

Structural and Functional Insights into Targeting GCCG Sites in the EGFR Promoter by Two DNA Intercalators to Inhibit Breast Cancer Metastasis.

Chih-Chun Chang, Hsin-Ju Li, Roshan Satange, Shan-Meng Lin, Tai-Lin Chen, Chi-Chien Lin, Stephen Neidle, Ming-Hon Hou

Abstract read
In one paragraph

Article in Journal of medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
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.

Chih-Chun ChangGraduate Institute of Biotechnology, National Chung Hsing University, Taichung 402, Taiwan.
Hsin-Ju LiGraduate Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 402, Taiwan.
Roshan SatangeGraduate Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 402, Taiwan.ORCID 0000-0002-5150-9363
Shan-Meng LinGraduate Institute of Genomics and Bioinformatics, National Chung Hsing University, Taichung 402, Taiwan.
Tai-Lin ChenPost Baccalaureate Medicine, School of Medicine, National Chung Hsing University, Taichung 402, Taiwan.
Chi-Chien LinInstitute of Biomedical Science, National Chung Hsing University, Taichung 402, Taiwan.
Stephen NeidleThe School of Pharmacy, University College London, London WC1N 1AX, U.K.ORCID 0000-0003-0622-6548
Ming-Hon HouGraduate Institute of Biotechnology, National Chung Hsing University, Taichung 402, Taiwan.ORCID 0000-0003-4170-1527

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemotherapeutic drugs are commonly used to treat cancers lacking targeted therapy options. However, their low specificity limits their treatment effectiveness. We report here that the cooperative binding of doxorubicin (Dox) with actinomycin D (ActD) enhances the specificity for consecutive GCCG sites in DNA. Using X-ray crystallography, we determined the crystal structure of ActD and Dox bound to d(AGCCGT)

Indexed as

DactinomycinDoxorubicinErbB ReceptorsIntercalating AgentsPromoter Regions, GeneticAnimalsAntineoplastic AgentsBreast NeoplasmsCell Line, TumorCrystallography, X-RayDNAFemaleHumansMiceMice, NudeNeoplasm MetastasisAntineoplastic AgentsDactinomycinDNADoxorubicinEGFR protein, humanErbB ReceptorsIntercalating Agents

Identifiers

PMID40032551
PMCPMC11956004

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.