Evidence map›Paper›PMID 40649817›Full record

ArticleInternational journal of molecular sciences2025

Quinazolinedione Derivatives as Potential Anticancer Agents Through Apoptosis Induction in MCF-7.

Tanapol Limboonreung, Teetat Suansilpong, Panitan Jumjitvi, Duangporn Lohawittayanan, Sucheewin Krobthong, Sitthivut Charoensutthivarakul

Abstract read
In one paragraph

Article in International journal of molecular sciences, 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

6 authors.

Tanapol LimboonreungSchool of Dentistry, King Mongkut's Institute of Technology Ladkrabang, Chalongkrung Road, Ladkrabang, Bangkok 10520, Thailand.
Teetat SuansilpongSchool of Dentistry, King Mongkut's Institute of Technology Ladkrabang, Chalongkrung Road, Ladkrabang, Bangkok 10520, Thailand.
Panitan JumjitviSchool of Dentistry, King Mongkut's Institute of Technology Ladkrabang, Chalongkrung Road, Ladkrabang, Bangkok 10520, Thailand.ORCID 0009-0005-2353-9863
Duangporn LohawittayananInnovative Molecular Discovery Laboratory (iMoD), School of Bioinnovation and Bio-Based Product Intelligence, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.
Sucheewin KrobthongDepartment of Chemistry, Faculty of Science, Chulalongkorn University, Bangkok 10330, Thailand.ORCID 0000-0003-4428-4140
Sitthivut CharoensutthivarakulInnovative Molecular Discovery Laboratory (iMoD), School of Bioinnovation and Bio-Based Product Intelligence, Faculty of Science, Mahidol University, Bangkok 10400, Thailand.ORCID 0000-0002-4447-3438

Funding

King Mongkut Institute of Technology Ladkrabang Research Fund KREF186510Mahidol University (Basic Research Fund: fiscal year 2021) BRF1-A23/2564
6 · The paper itself

Abstract

Breast cancer remains a leading cause of mortality among women worldwide. Surgery, radiation therapy, chemotherapy, and hormone-based treatments are standard therapeutic approaches, but drug resistance and adverse effects necessitate the search for novel anticancer agents. Quinazolinedione derivatives have emerged as potential anticancer compounds due to their cytotoxic and apoptosis-inducing properties. This study aimed to evaluate the apoptotic induction of previously reported quinazolinedione derivatives on MCF-7 breast cancer cells. The cytotoxic effect was assessed using the MTT assay, apoptosis was quantified by Annexin V-PE/7AAD staining and flow cytometry, and apoptosis-related protein expression was analyzed via multiplexed bead-based immunoassays. These findings indicate that two derivatives in the series significantly reduced the cell viability in a dose-dependent manner. Apoptosis was induced primarily through the intrinsic apoptotic pathway as evidenced by the upregulation of caspase-9 and p53 and the downregulation of Bcl-2 and p-Akt. These results highlight quinazolinedione derivatives as promising candidates for breast cancer therapy prompting further investigation into their molecular mechanisms and potential clinical applications.

Indexed as

Antineoplastic AgentsApoptosisBreast NeoplasmsQuinazolinonesCaspase 9Cell ProliferationCell SurvivalFemaleHumansMCF-7 CellsProto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2Tumor Suppressor Protein p53Antineoplastic AgentsCaspase 9Proto-Oncogene Proteins c-aktProto-Oncogene Proteins c-bcl-2QuinazolinonesTumor Suppressor Protein p53breast cancercaspase activationMCF-7programmed cell deathquinazolinedione derivatives

Identifiers

PMID40649817
PMCPMC12250072

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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.