Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021 Jun 20;69(1):16.
doi: 10.1007/s00005-021-00618-5.

CTLA-4 Expression and Its Clinical Significance in Breast Cancer

Affiliations
Free article

CTLA-4 Expression and Its Clinical Significance in Breast Cancer

Rodrigo Kern et al. Arch Immunol Ther Exp (Warsz). .
Free article

Abstract

Breast cancer is the leading cause of women's death among all cancers. The main reason associated with this is the development of metastasis and therapy-resistant breast carcinoma (BC), which pose the main challenge of oncology nowadays. Evidence suggest that these tumors seem to have inhibitory mechanisms that may favor their progression and surveillance. Cancer cells can evade antitumor T cell responses by expressing some immune inhibitory molecules such as the cytotoxic T-lymphocyte antigen-4 (CTLA-4), whose clinical meaning has emerged in the last few years and is poorly understood in the BC context. This systematic literature review aims at identifying studies on CTLA-4 expression in BC, and address what is known about its clinical meaning. A literature search was performed in PubMed and LILACS databases, using the MESH terms "breast cancer"; "CTLA-4 Antigen/antagonists and inhibitors"; and "Lymphocytes, Tumor-Infiltrating/immunology", published in the last 10 years. In total, 12 studies were included in this review. Systematic review used the Preferred Reporting Items for Systematic Reviews and Meta-Analyses. Despite the small number of eligible studies, the literature reports some associations between CTLA-4 expression in the tumor microenvironment and worse BC outcomes, regardless of its molecular subtype. CTLA-4 expression in BC is a putative marker of clinical significance and a rationale therapeutic target in the emerging field of immunotherapy.

Keywords: Breast neoplasms; CTLA-4 antigen/antagonists and inhibitors; Flow cytometry; Immunohistochemistry; Ipilimumab; Lymphocytes; Tumor-infiltrating/immunology.

PubMed Disclaimer

References

    1. Abdou Y, Pandey M, Sarma M et al (2020) Mechanism-based treatment of cancer with immune checkpoint inhibitor therapies. Br J Clin Pharmacol 86:1690–1702 - DOI
    1. Ács B, Madaras L, Tőkés AM et al (2017) PD-1, PD-L1 and CTLA-4 in pregnancy-related and in early-onset breast cancer: a comparative study. Breast 35:69–77. https://doi.org/10.1016/j.breast.2017.06.013 - DOI - PubMed
    1. Adams S, Gray RJ, Demaria S et al (2014) Prognostic value of tumor-infiltrating lymphocytes in triple-negative breast cancers from two phase III randomized adjuvant breast cancer trials: ECOG 2197 and ECOG 1199. J Clin Oncol 32:2959–2966. https://doi.org/10.1200/JCO.2013.55.0491 - DOI - PubMed - PMC
    1. Barber DL, Wherry EJ, Masopust D et al (2006) Restoring function in exhausted CD8 T cells during chronic viral infection. Nature 439:682–687. https://doi.org/10.1038/nature04444 - DOI - PubMed
    1. Bhandaru M, Rotte A (2019) Monoclonal antibodies for the treatment of melanoma: present and future strategies. Methods Mol Biol 1904:83–108. https://doi.org/10.1007/978-1-4939-8958-4_4 - DOI - PubMed

Publication types

MeSH terms

LinkOut - more resources