Câncer de mama e modulação imunológica: o papel do exercício físico na via PD-1/PD-L1 e suas implicações terapêuticas

Autores

  • Bruna Queiroz Couto Fujimura
  • João Víctor Pires Silva
  • Eduardo Elias Vieira de Carvalho
  • Douglas Reis Abdalla Universidade Federal do Triângulo Mineiro

DOI:

https://doi.org/10.5281/zenodo.19110578

Palavras-chave:

câncer de mama, PD-1/PD-L1, Imunoterapia, Exercício Físico, Microambiente tumora

Resumo

O câncer de mama representa a segunda neoplasia mais incidente globalmente, constituindo a principal causa de mortalidade oncológica feminina no Brasil. Este estudo apresenta o panorama epidemiológico dos subtipos mais agressivos de câncer de mama e analisa o papel do sistema imunológico na vigilância tumoral. Os subtipos mais agressivos incluem o inflamatório (2-4% dos casos), triplo-negativo (15%) e HER2 positivo, caracterizados por alta taxa de metástase e prognóstico desfavorável. O sistema imunológico exerce papel fundamental na progressão da doença, sendo os linfócitos infiltrantes no tumor (TILs) associados a prognósticos favoráveis, especialmente nos subtipos triplo-negativo e HER2 positivo. A via PD-1/PD-L1 constitui mecanismo central de escape imunológico, sendo alvo de imunoterapias que bloqueiam essa interação para potencializar a resposta antitumoral. O exercício físico emerge como estratégia complementar importante, demonstrando efeitos benéficos na redução de fatores de risco modificáveis e melhoria da qualidade de vida durante o tratamento. Estudos indicam que a atividade física pode modular a expressão de PD-1/PD-L1 no microambiente tumoral, promovendo melhor infiltração de células T citotóxicas e potencializando a eficácia das imunoterapias. A integração entre exercício físico e imunoterapia representa abordagem promissora no tratamento do câncer de mama, especialmente nos subtipos mais agressivos.

Downloads

Não há dados estatísticos.

Referências

Abdalla DR, Murta EFC, Michelin MA. The influence of physical activity on the profile of immune response cells and cytokine synthesis in mice with experimental breast tumors induced by 7,12-dimethylbenzanthracene. Eur J Cancer Prev. 2013;22(3):251-8. doi:10.1097/CEJ.0b013e3283592cbb

Abdalla DR, Aleixo AAR, Murta EFC, Michelin MA. Innate immune response adaptation in mice subjected to administration of DMBA and physical activity. Oncol Lett. 2014;7(3):886-90. doi:10.3892/ol.2013.1774

Abdalla DR, Aleixo AAR, Murta EFC, Michelin MA. The Influence Of Exercise On The Immune Response Cells In Mice With Experimental Tumor Induced By 4T1 Cell Line. In: Anais do IV International Symposium on Translational Oncology; 2014; Barretos. Barretos: Hospital de Câncer de Barretos; 2014.

Afolabi LO, et al. MDSC checkpoint blockade therapy: a new breakthrough point overcoming immunosuppression in cancer immunotherapy. Cancer Gene Ther. 2025;32(3):471-90. doi:10.1038/s41417-025-00886-9

Agussalim NQ, et al. Atividade física e qualidade de vida em sobreviventes de câncer de mama. Doença da Mama. 2024;43:161-71. doi:10.3233/BD-249005

Alves MJM, et al. Os Benefícios dos Exercícios Físicos no Câncer de Mama. Arq Bras Cardiol. 2022.

Alves RS, et al. Influence of an Exergaming Training Program on Reducing the Expression of IL-10 and TGF-β in Cancer Patients. Games Health J. 2020;9(6):446-52. doi:10.1089/g4h.2019.0195

Baker K, Powis SJ, Lewis JD. Human breast tumor-infiltrating CD8+ T cells retain polyfunctionality despite PD-1 expression. Nat Commun. 2018;9:4143. doi:10.1038/s41467-018-06653-9

Barili V, et al. Genetic basis of breast and ovarian cancer: approaches and lessons learnt from three decades of inherited predisposition testing. Genes. 2024;15(2):219. doi:10.3390/genes15020219

Barroso-Sousa R, Tolaney SM. Clinical development of PD-1/PD-L1 inhibitors in breast cancer: still a long way to go. Curr Breast Cancer Rep. 2020;12:1-8. doi:10.1007/s11864-020-00756-6

Raman R, Debata S, Govindarajan T, Kumar P. Targeting Triple-Negative Breast Cancer: Resistance Mechanisms and Therapeutic Advancements. Cancer Med. 2025 May;14(9):e70803.

Bianco TM, Abdalla DR, Desidério CS, et al. The influence of physical activity in the anti-tumor immune response in experimental breast tumor. Immunol Lett. 2017;190:148-58. doi:10.1016/j.imlet.2017.08.007

Cerqueira É, et al. Inflammatory effects of high and moderate intensity exercise - A systematic review. Front Physiol. 2020;11:1666. doi:10.3389/fphys.2020.01666

Chen X, et al. Mechanisms and strategies to overcome PD-1/PD-L1 blockade resistance in triple-negative breast cancer. Cancers. 2022;15(1):104.

Ciarka A, Piątek M, Pęksa R, Kunc M, Senkus E. Tumor-Infiltrating Lymphocytes (TILs) in Breast Cancer: Prognostic and Predictive Significance across Molecular Subtypes. Biomedicines. 2024;12(4):763. doi:10.3390/biomedicines12040763

Cohen SY, et al. Modifiable risk factors in women at high risk of breast cancer: a systematic review. Breast Cancer Res. 2023;25(1):45.

Colpani V, et al. Impact of exercise on cancer: mechanistic perspectives and new insights. Front Immunol. 2024;15:1474770. doi:10.3389/fimmu.2024.1474770

Cortes J, Rugo HS, Cescon DW, et al. Pembrolizumab plus Chemotherapy in Advanced Triple-Negative Breast Cancer. N Engl J Med. 2022;387(3):217-26. doi:10.1056/NEJMoa2202809

Cortes J, et al. Pembrolizumab plus chemotherapy in advanced triple-negative breast cancer. N Engl J Med. 2024;390:242-51.

Corti C, et al. Recent Advances in Immune Checkpoint Inhibitors for Triple-Negative Breast Cancer. Immunotargets Ther. 2025 Apr 3;14:339-357.

De Oliveira Otto ACP, et al. Physical exercise and immune system in cancer: an integrative review. Front Oncol. 2021;11:724424. doi:10.3389/fonc.2021.724424

Denkert C, von Minckwitz G, Darb-Esfahani S, et al. Tumour-infiltrating lymphocytes and prognosis in different subtypes of breast cancer: a pooled analysis of 3771 patients treated with neoadjuvant therapy. Lancet Oncol. 2018;19(1):40-50. doi:10.1016/S1470-2045(17)30904-X

Diaz-Montero CM, et al. Myeloid-derived suppressor cells in cancer: therapeutic targets to overcome tumor immune evasion. Mol Cancer. 2024;23(1):89.

Dieli-Conwright CM, et al. Effect of Exercise on Markers of Inflammation in Breast Cancer Survivors: The Yale Exercise and Survivorship Study. Cancer Epidemiol Biomarkers Prev. 2020;29(5):1056-64. doi:10.1158/1055-9965.EPI-19-1462

Fjørtoft MO, Huse K, Otterlei M. The tumor immune microenvironment in breast cancer progression. Acta Oncol. 2024;63:33008. doi:10.2340/1651-226X.2024.33008

Gabrilovich DI. Myeloid-derived suppressor cells as immunosuppressive regulators and therapeutic targets in cancer. Signal Transduct Target Ther. 2021;6(1):362.

Gagliato DM, Gonzalez-Angulo AM, Lei X, et al. Clinical impact of delaying initiation of adjuvant chemotherapy in patients with breast cancer. J Clin Oncol. 2017;32(8):735-44. doi:10.1200/JCO.2013.49.7693

Gagliato DM, et al. Tumor-infiltrating lymphocytes in Breast Cancer and implications for clinical practice. Biochim Biophys Acta Rev Cancer. 2017;1868(2):527-37. doi:10.1016/j.bbcan.2017.10.003

García LS, et al. Patterns of immune evasion in triple-negative breast cancer and new potential therapeutic targets: a review. Front Immunol. 2024;15:1513421. doi:10.3389/fimmu.2024.1513421

Garrido F, et al. HLA class I alterations in breast carcinoma: mechanisms and clinical implications. Clin Cancer Res. 2024;30(5):891-903.

Ge J, et al. Regulatory T cells: masterminds of immune equilibrium and future therapeutic innovations. Front Immunol. 2024;15:1457189.

Ge LP, Jin X, Ma D, et al. ZNF689 deficiency promotes intratumor heterogeneity and immunotherapy resistance in triple-negative breast cancer. Cell Res. 2024;34(1):58-75.

Gil del Alcazar CR, et al. Immune escape during breast tumor progression. Cancer Immunol Res. 2020;8(4):422-7.

Gil del Alcazar CR, et al. Immune escape in breast cancer during in situ to invasive carcinoma transition. Cancer Discov. 2017;7(10):1098-115.

Guerra RL, et al. Impacto do treinamento com pesos na força muscular em idosas: uma revisão sistemática. Rev Bras Ciênc Esporte. 2019;41(3):320-8.

Harris MA, et al. Towards targeting the breast cancer immune microenvironment. Nat Rev Cancer. 2024;24(8):554-77. doi:10.1038/s41568-024-00714-6

Heater NK, Warrior S, Lu J. Current and future immunotherapy for breast cancer. J Hematol Oncol. 2024;17(1):131. doi:10.1186/s13045-024-01649-z

Hoechst B, et al. Crosstalk between regulatory T cells and myeloid-derived suppressor cells during melanoma growth. OncoImmunology. 2013;2(8):e25940.

Hojman P, Gehl J, Christensen JF, Pedersen BK. Molecular Mechanisms Linking Exercise to Cancer Prevention and Treatment. Cell Metab. 2020;27(1):10-21. doi:10.1016/j.cmet.2017.09.015

Huertas-Caro CA, et al. Tumor infiltrating lymphocytes (TILs) are a prognosis biomarker in Colombian patients with triple negative breast cancer. Sci Rep. 2023;13(1):21324.

Instituto Nacional de Câncer (Brasil). Controle do câncer de mama no Brasil: dados e números 2024. Rio de Janeiro: INCA; 2024.

Javed SA, Najmi A, Ahsan W, Zoghebi K. Targeting PD-1/PD-L-1 immune checkpoint inhibition for cancer immunotherapy: success and challenges. Front Immunol. 2024;15:1383456. doi:10.3389/fimmu.2024.1383456

Kamphorst AO, et al. Metabolic immunoengineering approaches to enhance CD8+ T cell-based cancer immunotherapy. Cell Syst. 2024;15(12):1147-65. doi:10.1016/j.cels.2024.11.007

Khosravi N, et al. Exercise training, circulating cytokine levels and immune function in cancer survivors: A meta-analysis. Brain Behav Immun. 2019;81:92-104. doi:10.1016/j.bbi.2019.08.187

Khoury T, et al. Prognostic significance of stromal versus intratumoral infiltrating lymphocytes in different subtypes of breast cancer treated with cytotoxic neoadjuvant chemotherapy. Appl Immunohistochem Mol Morphol. 2018;26(7):523-32.

Kim C, Gao R, Sei E, et al. Chemoresistance Evolution in Triple-Negative Breast Cancer Delineated by Single-Cell Sequencing. Cell. 2021;173(4):879-93. doi:10.1016/j.cell.2018.03.041

Kim SI, et al. Tumor burden and immunotherapy: impact on immune infiltration and therapeutic outcomes. Front Immunol. 2021;11:629722. doi:10.3389/fimmu.2020.629722

Koivula T, et al. The effect of exercise and disease status on mobilization of anti-tumorigenic and pro-tumorigenic immune cells in women with breast cancer. Front Immunol. 2024;15:1394420. doi:10.3389/fimmu.2024.1394420

Kotoula V, Chatzopoulos K, Lakis S, et al. Tumors with high-density tumor infiltrating lymphocytes constitute a favorable entity in breast cancer: a pooled analysis of four prospective adjuvant trials. Ann Oncol. 2016;27(2):259-71. doi:10.1093/annonc/mdv370

Kraja A, et al. Tumor-infiltrating lymphocytes in cancer immunotherapy: from chemotactic recruitment to translational modeling. Front Immunol. 2025;16:1601773. doi:10.3389/fimmu.2025.1601773

Ladoire S, et al. In situ immune response after neoadjuvant chemotherapy for breast cancer predicts survival. J Pathol. 2011;224(3):389-400.

Lee JY, Chung YS, Jung SY. Effects of high-intensity focused ultrasound (HIFU) treatment for skin tightening and rejuvenation in Asian skin. J Cosmet Dermatol. 2022;21(1):107-12.

Leon-Ferre RA, et al. Advances in systemic therapies for triple negative breast cancer. BMJ. 2023;381:e071674. doi:10.1136/bmj-2022-071674

Li S, et al. Regulatory mechanisms of PD-1/PD-L1 in cancers. Mol Cancer. 2024;23:108. doi:10.1186/s12943-024-02023-w

Li X, et al. Prognostic value and distribution pattern of tumor infiltrating lymphocytes and their subsets in distant metastases of advanced breast cancer. Clin Breast Cancer. 2024;24(1):e45-e54.

Li Y, et al. Tumor mutational burden predicting the efficacy of immune checkpoint inhibitors in colorectal cancer: a systematic review and meta-analysis. Front Immunol. 2021;12:751407.

Li Z, Liu J, Zhang Y, et al. Immune checkpoint inhibitors and HER2-targeted therapy in HER2-positive breast cancer. Cancer Med. 2021;10(11):3694-708. doi:10.1002/cam4.3924

Liu G, Zhang Y, Huang Y. Triple-Negative Breast Cancer Treatment Advancements: A Review of Evolving Strategies. Eur J Cancer Care. 2024. doi:10.1155/2024/8299502

Loibl S, et al. Early breast cancer: ESMO Clinical Practice Guideline for diagnosis, treatment and follow-up. Ann Oncol. 2024;35(2). doi:10.1016/j.annonc.2023.11.016

Loi S, Drubay D, Adams S, et al. Prognostic Value of Tumor-Infiltrating Lymphocytes for Patients With Triple-Negative Breast Cancer. JAMA Oncol. 2024;10(4):450-9. doi:10.1001/jamaoncol.2023.7289

Loi S, et al. Tumor-infiltrating lymphocytes and prognosis: a pooled individual patient analysis of early-stage triple-negative breast cancers. J Clin Oncol. 2019;37(7):559-69.

Mariathasan S, et al. TGFβ attenuates tumour response to PD-L1 blockade by contributing to exclusion of T cells. Nature. 2018;554(7693):544-8.

Marques-Bessa D, et al. Breaking Barriers: The Promise and Challenges of Immune Checkpoint Inhibitors in Triple-Negative Breast Cancer. Biomedicines. 2024;12(2):369.

McGranth DJ, et al. Multi-omics analysis reveals neoantigen-independent immune cell infiltration in copy-number driven cancers. Nat Commun. 2018;9(1):1317.

Melisi D, et al. Galunisertib plus gemcitabine vs. gemcitabine for first-line treatment of patients with unresectable pancreatic cancer. Br J Cancer. 2024;130(2):234-42.

Mirlekar B. Tumor promoting roles of IL-10, TGF-β, IL-4, and IL-35: Its implications in cancer immunotherapy. SAGE Open Med. 2022;10:20503121211069012.

Mlynska A, et al. Exercise-induced extracellular vesicles delay tumor development by igniting inflammation in an immunologically cold triple-negative breast cancer mouse model. J Sport Health Sci. 2025;14:101041. doi:10.1016/j.jshs.2025.01.008

Naji O, et al. Investigating tumor immunogenicity in breast cancer: deciphering the tumor immune response to enhance therapeutic approaches. Front Immunol. 2024;15:1399754.

Obeagu EI, Obeagu GU. Lymphocyte infiltration in breast cancer: A promising prognostic indicator. Medicine (Baltimore). 2024;103(49):e40845. doi:10.1097/MD.0000000000040845

Planes-Laine G, et al. PD-1/PD-L1 Targeting in Breast Cancer: The First Clinical Evidences are Emerging—A Literature Review. Cancers. 2019;11(7):1033.

Plitas G, Rudensky AY. Regulatory T cells in cancer. Annu Rev Cancer Biol. 2020;4:459-77.

Poikonen-Saksela P, et al. Associations between Physical Exercise, Quality of Life, Psychological Symptoms and Treatment Side Effects in Early Breast Cancer. Cancers. 2022.

Prestes J, et al. Câncer: benefícios do treinamento de força e aeróbio. Rev Bras Med Esporte. 2010.

Pupa SM, et al. HER2 signaling and breast cancer stem cells: the bridge behind HER2-positive breast cancer aggressiveness and therapy refractoriness. Cancers. 2021;13(19):4778. doi:10.3390/cancers13194778

Rodrigues GNC, et al. Head and Neck Tumors Associated with Human Papillomavirus Infection: A Literary Review Addressing Immunotherapy for Checkpoints. Adv Cancer Res Clin Imaging. 2021;3:1-6.

Salgado R, et al. The evaluation of tumor-infiltrating lymphocytes (TILs) in breast cancer: recommendations by an International TILs Working Group 2014. Ann Oncol. 2015;26(2):259-71.

Salgado R, et al. Harnessing Tumor-Infiltrating Lymphocytes in Triple-Negative Breast Cancer: Opportunities and Barriers to Clinical Integration. Int J Mol Sci. 2025;26(9):4292.

Sami A, Raza A. Reprogramming the tumor microenvironment – macrophages emerge as key players in breast cancer immunotherapy. Front Immunol. 2024;15:1457491. doi:10.3389/fimmu.2024.1457491

Sanmamed MF, Chen L. A paradigm shift in cancer immunotherapy: from enhancement to normalization. Cell. 2018;175(2):313-26. doi:10.1016/j.cell.2018.09.035

Savas P, Caramia F, Teo ZL, et al. Oncogene addiction and immunity: Mechanisms and implications. Curr Opin Oncol. 2016;28(6):562-7. doi:10.1097/CCO.0000000000000131

Savas P, et al. The anti-cancer immune response in breast cancer: current and emerging biomarkers and treatments. Trends Cancer. 2024;10(6):490-506.

Schmid P, Adams S, Rugo HS, et al. Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer. N Engl J Med. 2018;379(22):2108-21. doi:10.1056/NEJMoa1809615

Schmid P, Cortes J, Dent R, et al. Event-free Survival with Pembrolizumab in Early Triple-Negative Breast Cancer. N Engl J Med. 2024;386(6):556-67. doi:10.1056/NEJMoa2112651

Serafini P, et al. Myeloid-derived suppressor cells promote cross-tolerance in B-cell lymphoma by expanding regulatory T cells. Cancer Res. 2013;68(13):5439-49.

Serafini P, et al. Phosphodiesterase-5 inhibition augments endogenous antitumor immunity by reducing myeloid-derived suppressor cell function. J Exp Med. 2006;203(12):2691-702.

Sharma P, et al. PD-1/PD-L1 immune checkpoint blockade in breast cancer: research insights and sensitization strategies. Mol Cancer. 2022;21(1):178.

Silva CAA, et al. Influence of Physical Activity in Patients with Prostate Cancer Undergoing Radiotherapy and/or Hormonal Deprivation Therapy: Integrative Literature Review. Int J Sports Exerc Med. 2021;7:1-6.

Silva MP, et al. Physical Exercise and the Hallmarks of Breast Cancer: A Narrative Review. Cancers. 2024.

Silveira MP, et al. Physical exercise as a tool to help the immune system against COVID-19: an integrative review of the current literature. Clin Exp Med. 2021;21(1):1-9. doi:10.1007/s10238-020-00670-1

Solinas C, Gombos A, Latifyan S, et al. Significance of TILs in breast cancer: understanding immune infiltrate assembly and activation status. Ann Oncol. 2017;28(6):1159-68. doi:10.1093/annonc/mdx073

Solinas C, et al. Immune checkpoint molecules on tumor-infiltrating lymphocytes and their association with tertiary lymphoid structures in human breast cancer. Front Immunol. 2017;8:1412.

Southey MC, et al. PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS. J Med Genet. 2016;53(4):221-9.

Spirandelli LCD, Soares MB, Alves OC, et al. Influence of Exercise or Physical Activity in the Angiogenesis Process: Integrative Review. Online J Cardiovasc Res. 2020;3(5):1-9. doi:10.33552/OJCR.2020.03.000574

Spirandelli LCD, Veloso VB, Carvalho EEV, et al. Transient Immune Deficit after Exercise and the Relationship with Immuno-Nutrition: A Short Review of the Literature. Int J Sports Exerc Med. 2020;6:172. doi:10.23937/2469-5718/1510172

Sun W, Wang H, Qi Y, et al. Progress of PD-1/PD-L1 immune checkpoint inhibitors in the treatment of triple-negative breast cancer. Cancer Cell Int. 2025;25(1):30. doi:10.1186/s12935-025-03769-z

Sung, H. et al. Global Cancer Statistics 2020: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA: A Cancer Journal for Clinicians, v. 71, n. 3, p. 209-249, 2021.

Tarekegn K, et al. The role of immune checkpoint inhibition in triple negative breast cancer. Expert Opin Drug Dev. 2023;23(10):1095-106. doi:10.1080/14737140.2023.2265059

Terra R, et al. Efeito do exercício no sistema imune: resposta, adaptação e sinalização celular. Rev Bras Med Esporte. 2012;18(3):208-13.

Veglia F, Sanseviero E, Gabrilovich DI. Myeloid-derived suppressor cells in the era of increasing myeloid cell diversity. Nat Rev Immunol. 2021;21(8):485-98.

Wang J, Chen Y, Liu Y, et al. PD-1/PD-L1 immune checkpoint blockade in breast cancer: research insights and sensitization strategies. Mol Cancer. 2024;23(1):241. doi:10.1186/s12943-024-02176-8

Wang J, et al. Exercise regulates the immune system. Adv Exp Med Biol. 2020;1220:31-45. doi:10.1007/978-3-030-29663-9_4

Wang K, et al. Expert consensus on the clinical application of immunotherapy in breast cancer: 2024. Transl Breast Cancer Res. 2024;5:9. doi:10.21037/tbcr-24-15

Wang M, et al. Mechanism of immune evasion in breast cancer. OncoTargets Ther. 2017;10:1561-73.

Wang X, et al. Visando vias de sinalização no câncer de mama inflamatório. Cancers. 2020;12(9):2479. doi:10.3390/cancers12092479

Wang Y, et al. Anti-inflammatory effects of exercise in chronic disease. Front Physiol. 2020;11:566.

Wennerberg E, Lhuillier C, Rybstein MD, et al. Exercise reduces immune suppression and breast cancer progression in a preclinical model. Oncotarget. 2020;11(4):452-61. doi:10.18632/oncotarget.27464

Wennerberg E, et al. Exercise reduces immune suppression and breast cancer progression in a preclinical model. Clin Cancer Res. 2020;26(13):3435-49. doi:10.1158/1078-0432.CCR-19-2398

Wofford W, et al. Alterations of ceramide synthesis induce PD-L1 internalization and signaling to regulate tumor metastasis and immunotherapy response. Cell Rep. 2024;43(8):114532. doi:10.1016/j.celrep.2024.114532

Xu Y, et al. Interleukin signaling in the regulation of natural killer cells biology in breast cancer. Front Immunol. 2024;15:1467621. doi:10.3389/fimmu.2024.1467621

Yang T, et al. Immunotherapy targeting PD-1/PD-L1 in early-stage triple-negative breast cancer. J Pers Med. 2023;13(3):526. doi:10.3390/jpm13030526

Yi M, et al. Combination strategies with PD-1/PD-L1 blockade: current advances and future directions. J Cancer Res Clin Oncol. 2022;148:11-28. doi:10.1007/s00432-021-03644-1

Yu J, et al. Tumor-infiltrating Treg, MDSC, and IDO expression associated with outcomes of neoadjuvant chemotherapy of breast cancer. N Engl J Med. 2018;22(8):e165095. doi:10.1158/2326-6066.CIR-17-0144

Zheng Y, et al. Molecular mechanisms of immunotherapy resistance in triple-negative breast cancer. Front Immunol. 2023;14:1153990. doi:10.3389/fimmu.2023.1153990

Downloads

Publicado

2026

Como Citar

QUEIROZ COUTO FUJIMURA, Bruna; PIRES SILVA, João Víctor; VIEIRA DE CARVALHO, Eduardo Elias; ABDALLA, Douglas Reis. Câncer de mama e modulação imunológica: o papel do exercício físico na via PD-1/PD-L1 e suas implicações terapêuticas. Cadernos de InterPesquisas, [S. l.], v. 4, p. 074–102, 2026. DOI: 10.5281/zenodo.19110578. Disponível em: https://esabere.ojs.com.br/index.php/cadips/article/view/207. Acesso em: 16 abr. 2026.

Edição

Seção

Artigos de Fluxo Contínuo

Artigos Semelhantes

Você também pode iniciar uma pesquisa avançada por similaridade para este artigo.