Evidence map›Paper›PMID 39041268›Full record

ArticleCurrent pharmaceutical design2024

Doxorubicin-induced Immunogenic Cell Death Impairs Tumor Progression and Distant Metastasis in a 4T1 Breast Cancer Tumor Model.

Camila Magalhães Cardador, Thaís Bergmann de Castro, Raffael Júnio Araújo de Castro, Anamélia Lorenzetti Bocca, Luana Cristina Camargo, Thyago Arruda Pacheco, Luís Alexandre Muehlmann, João Paulo Figueiró Longo

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Article in Current pharmaceutical design, 2024. 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. Degraded sulfated galactan derived fromMolecular medicine reports · 2026
    Article
  3. 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.

Camila Magalhães CardadorDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, Brasília, Brazil.
Thaís Bergmann de CastroDepartment of Cellular Biology, Institute of Biological Sciences, University of Brasilia, Brasília, Brazil.
Raffael Júnio Araújo de CastroDepartment of Cellular Biology, Institute of Biological Sciences, University of Brasilia, Brasília, Brazil.
Anamélia Lorenzetti BoccaDepartment of Cellular Biology, Institute of Biological Sciences, University of Brasilia, Brasília, Brazil.
Luana Cristina CamargoDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, Brasília, Brazil.
Thyago Arruda PachecoDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, Brasília, Brazil.
Luís Alexandre MuehlmannDepartment of Genetics and Morphology, Faculty of Ceilândia, University of Brasília, Brasília, Brazil.
João Paulo Figueiró LongoDepartment of Genetics and Morphology, Institute of Biological Sciences, University of Brasília, Brasília, Brazil.

Funding

Conselho Nacional de Desenvolvimento Científico e Tecnológico 3056172022Fundação de Apoio à Pesquisa do Distrito Federal 00193-00000734/2021-75,00193-00001826/2023-34
6 · The paper itself

Abstract

introductionCancer is an individual disease and its formation and development are specific to each host. Conventional treatments are ineffective in complex cases, such as metastasis, and have severe adverse side effects. New strategies are needed to address the problem, and the use of immunogenic cell death (ICD) as a trigger or booster of the immune system through the exposure of damage-associated molecular patterns, along with tumor antigens, by cancerous cells is presented as an immunization approach in this work.

methodsFor this purpose, 4T1 cells were exposed to doxorubicin (DOX) for 24 hours and then, these cells undergoing ICD were subcutaneously administered to mice. The ICD induction by DOX on 4T1 was assessed by flow cytometry and image analysis. This immunization process was performed three times and after the last administration, the immunized mice were challenged with a subcutaneous xenograft of live cancer cells.

resultsThe results demonstrate that the mice immunized with cells undergoing ICD after exposure to DOX presented no primary tumor or indications of distant metastatic lesion development.

conclusionIn summary, our findings indicate that the immunization process utilizing ICD is indeed efficacious in managing this aggressive form of pre-clinical breast cancer.

Indexed as

Breast NeoplasmsDoxorubicinMice, Inbred BALB CAnimalsAntibiotics, AntineoplasticCell Line, TumorDisease Models, AnimalDisease ProgressionFemaleHumansImmunogenic Cell DeathMiceNeoplasm MetastasisAntibiotics, AntineoplasticDoxorubicinbreast cancerimmunizationimmunogenic cell deathMetastasismolecular patterns.tumor progression

Identifiers

PMID39041268

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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.