Control of aggressive 4T1-luc metastatic breast cancer using immunogenic cell lysates generated with methotrexate

This study investigated a novel immunization therapy for pre-clinical aggressive metastatic breast cancer using immunogenic cell lysates derived from 4T1-luc cells treated with cisplatin and methotrexate, addressing the critical need for improved treatments given the poor prognosis associated with breast cancer metastasis and its significant mortality rate. Methotrexate, a conventional cytotoxic agent, demonstrated a previously unrecognized capacity to induce immunogenic cell lysates, presenting a potential drug repositioning opportunity. In a murine model of stage IV metastatic breast cancer, immunization with these lysates significantly reduced primary tumor growth and lung metastasis, as assessed by bioluminescence imaging. Immunization also modulated immune cell populations, reducing splenomegaly and hepatomegaly, and partially reversing the immunosuppressive phenotype associated with 4T1-luc tumor growth, as evidenced by cytokine profiling (IL-6 and IFN-γ) and flow cytometry analysis of CD4 + and CD8 + T cell subpopulations. Specifically, methotrexate-treated lysates induced a significant shift in CD4 + T cells towards an effector phenotype. These findings highlight the potential of this immunotherapy approach to improve breast cancer treatment outcomes and warrant further investigation.

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Institutions

Publication Details

Journal
Biomedicine & Pharmacotherapy
Published
2025-04-24
DOI
https://doi.org/10.1016/j.biopha.2025.118079
Citations
2
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
1.59

Funders

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article

Control of aggressive 4T1-luc metastatic breast cancer using immunogenic cell lysates generated with methotrexate

I Valente, Sônia Nair Báo, Marina M. Simões, Gabriel Ribeiro Farias et al.
2 citations
Biomedicine & Pharmacotherapy
Immunotherapy and Immune Responses
1.59
article

Control of aggressive 4T1-luc metastatic breast cancer using immunogenic cell lysates generated with methotrexate

I Valente, Sônia Nair Báo, Marina M. Simões, Gabriel Ribeiro Farias, Karen L. R. Paiva, Luís Alexandre Muehlmann, Raffael Júnio Araújo de Castro, João Paulo Figueiró Longo, Luana Cristina Camargo, Victor Carlos Mello da Silva, Pierre‐Régis Burgel, Camila Magalhães Cardador, Tialfi Bergamin de Castro
article en
2 citations

Abstract

This study investigated a novel immunization therapy for pre-clinical aggressive metastatic breast cancer using immunogenic cell lysates derived from 4T1-luc cells treated with cisplatin and methotrexate, addressing the critical need for improved treatments given the poor prognosis associated with breast cancer metastasis and its significant mortality rate. Methotrexate, a conventional cytotoxic agent, demonstrated a previously unrecognized capacity to induce immunogenic cell lysates, presenting a potential drug repositioning opportunity. In a murine model of stage IV metastatic breast cancer, immunization with these lysates significantly reduced primary tumor growth and lung metastasis, as assessed by bioluminescence imaging. Immunization also modulated immune cell populations, reducing splenomegaly and hepatomegaly, and partially reversing the immunosuppressive phenotype associated with 4T1-luc tumor growth, as evidenced by cytokine profiling (IL-6 and IFN-γ) and flow cytometry analysis of CD4 + and CD8 + T cell subpopulations. Specifically, methotrexate-treated lysates induced a significant shift in CD4 + T cells towards an effector phenotype. These findings highlight the potential of this immunotherapy approach to improve breast cancer treatment outcomes and warrant further investigation.

Biomedicine & PharmacotherapyVol. 187
Universidade de Brasília (BR), Institute of Physics (AZ)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Financiadora de Estudos e Projetos, Fundação de Apoio à Pesquisa do Distrito Federal
Good health and well-being
Openalex Percentile: Top 18%
Immunotherapy and Immune Responses
1.59
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