Evidence map›Paper›PMID 40883339›Full record

ArticleScientific reports2025

A novel chromen-based small molecule induces apoptosis and modulates cellular response to triple-negative breast cancer.

Bernardine Tuah, Kwadwo Fosu, Diana Ahu Prah, Bright Kwame Yayra Hodogbe, Alberta Serwaa, Jutsum Nii Kotei Amon, Daniel Moscoh Ayine-Tora, Richard Kwamla Amewu, Kwabena Amofa Nketia Sarpong, Anastasia Rosebud Aikins

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Bernardine TuahWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Kwadwo FosuWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Diana Ahu PrahWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Bright Kwame Yayra HodogbeWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Alberta SerwaaWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Jutsum Nii Kotei AmonWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Daniel Moscoh Ayine-ToraDepartment of Chemistry, College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Richard Kwamla AmewuDepartment of Chemistry, College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana.
Kwabena Amofa Nketia SarpongWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana. kansarpong@ug.edu.gh.
Anastasia Rosebud AikinsWest African Centre for Cell Biology of Infectious Pathogens (WACCBIP), College of Basic and Applied Sciences, University of Ghana, Legon, Accra, Ghana. araikins@ug.edu.gh.

Funding

WACCBIP-World Bank ACE Masters/PhD fellowship WACCBI+NCDS; Awandare
6 · The paper itself

Abstract

Triple-negative breast cancer (TNBC) is challenging to treat due to its aggressive nature. Its lack of hormone receptors renders conventional therapies less effective. This study assessed the efficacy of a novel compound, compound 2, in modulating TNBC cell behaviour. We used in vitro assays with MDA-MB-468 and MDA-MB-231 cell lines. Methods included annexin V apoptosis assay, flow cytometry for cell cycle and qRT-PCR for gene expression. Clonogenic, adhesion and wound healing assays were used for phenotypic characterization. Cytokine and chemokine levels in MDA-MB-468 cells were also measured using a Luminex assay. Compound 2 increased both early and late apoptosis in cancer cells, particularly MDA MB 468 cells. It also upregulated pro-apoptotic genes while downregulating anti-apoptotic genes. Additionally, it induced G1-phase arrest in MDA MB 468 cells with downregulation in Ki67 expression. Compound 2 also reduced cancer stem cell populations, suppressed colony formation, and impaired cell migration at IC

Indexed as

Antineoplastic AgentsApoptosisTriple Negative Breast NeoplasmsCell Line, TumorCell MovementCell ProliferationCytokinesFemaleGene Expression Regulation, NeoplasticHumansAntineoplastic AgentsCytokinesApoptosisCell cycle arrestEpithelial-to-Mesenchymal transition (EMT)Stem-likeTriple-negative breast cancer

Identifiers

PMID40883339
PMCPMC12397266

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.