Evidence map›Paper›PMID 40108921›Full record

ArticleCurrent topics in medicinal chemistry2025

Multimodal Activity of a Novel Compound against Prostate and Pancreatic Cancer.

Flaviana Alves Dos Santos, Joelson Germano Crispim, Eduardo Davi Lima da Silva, Arsênio Rodrigues Oliveira, Aldilane Goncalves da Fonseca, Telma Maria Araujo Moura Lemos, Ana Cristina Lima Leite, Michelle Melgarejo da Rosa, Maira Galdino da Rocha Pitta, Michelly Cristiny Pereira and 2 more

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Article in Current topics in medicinal chemistry, 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

12 authors.

Flaviana Alves Dos SantosLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.
Joelson Germano CrispimLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0002-3057-1299
Eduardo Davi Lima da SilvaLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.
Arsênio Rodrigues OliveiraLaboratório de Planejamento em Química Medicinal (LpQM), Departamento de Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal de Pernambuco, 50740-520, Recife, PE, Brazil.
Aldilane Goncalves da FonsecaClinical Biochemistry Laboratory and Multidisciplinary Laboratory, Federal University of Rio Grande do Norte, Brazil.
Telma Maria Araujo Moura LemosClinical Biochemistry Laboratory and Multidisciplinary Laboratory, Federal University of Rio Grande do Norte, Brazil.
Ana Cristina Lima LeiteLaboratório de Planejamento em Química Medicinal (LpQM), Departamento de Ciências Farmacêuticas, Centro de Ciências da Saúde, Universidade Federal de Pernambuco, 50740-520, Recife, PE, Brazil.ORCID 0000-0002-9346-2292
Michelle Melgarejo da RosaLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0002-0163-3833
Maira Galdino da Rocha PittaLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0001-5881-0338
Michelly Cristiny PereiraLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0002-1672-8202
Ivan da Rocha PittaLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.
Moacyr Jesus Barreto de Melo RêgoLaboratory for Immunomodulation and New Therapeutic Approaches, Federal University of Pernambuco (UFPE), Recife, PE, Brazil.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProstate and pancreatic cancers pose significant global health challenges. This study explored the potential of compound 5b, a novel phthalimido-1,3-thiazole derivative, as an anticancer agent against these malignancies.

methodsIn vitro, compound 5b exhibited potent cytotoxic activity against both prostate (DU-145 and PC-3) and pancreatic (Panc-1 and Mia Paca-2) cancer cell lines. Notably, it significantly reduced colony formation in PC-3 cells, potentially hindering tumor growth. Furthermore, treatment with compound 5b suppressed cell migration and induced cell cycle arrest in the PC-3 line. Additionally, it triggered cell death through late apoptosis and necrosis at higher concentrations. Safety evaluations in mice revealed no mortality or adverse effects after a 30-day treatment with compound 5b. Key blood parameters (hematology) and biochemical markers of liver and kidney function remained unaltered.

resultsCompound 5b significantly reduced colony formation, suppressed cell migration, and induced cell cycle arrest and apoptosis/necrosis in prostate cancer cells. In vivo, safety evaluations showed no adverse effects in treated mice, with blood and biochemical markers remaining normal.

conclusionThese findings suggest that compound 5b holds promise for further development as a therapeutic option for prostate and pancreatic cancers. Its multimodal activity profile, targeting cell viability, migration, cell cycle progression, and cell death, warrants further investigation.

Indexed as

Antineoplastic AgentsPancreatic NeoplasmsProstatic NeoplasmsThiazolesAnimalsApoptosisCell Cycle CheckpointsCell Line, TumorCell MovementCell ProliferationDose-Response Relationship, DrugDrug Screening Assays, AntitumorHumansMaleMiceMolecular StructureAntineoplastic AgentsThiazolesAnti-tumor activitybiochemical markerscancercell cycle progressionchemotherapytargeting cell viability.

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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.