Effect of CCL5 expression in the recruitment of immune cells in triple negative breast cancer
Open accessAbstract
Triple negative breast cancer (TNBC) is the most aggressive form of breast cancer with limited options of targeted therapy. Recent findings suggest that the clinical course of TNBC may be modified by the presence of tumor-infiltrating lymphocytes (TILs) and chemokine’s expression, such as CCL5 . Diverse studies have shown that CCL5 suppresses anti-tumor immunity and it has been related to poor outcome in different types of cancer while in other studies, this gene has been related with a better outcome. We sought to determine the association of CCL5 with the recruitment of TILs and other immune cells. With this aim we evaluated a retrospective cohort of 72 TNBC patients as well as publicly available datasets. TILs were correlated with residual tumor size after neoadjuvant chemotherapy (NAC) and CCL5 expression. In univariate analysis, TILs and CCL5 were both associated to the distant recurrence free survival; however, in a multivariate analysis, TILs was the only significant marker (HR = 0.336; 95%IC: 0.150–0.753; P = 0.008). CIBERSORT analysis suggested that a high CCL5 expression was associated with recruitment of CD8 T cells, CD4 activated T cells, NK activated cells and macrophages M1. The CD8A gene (encoding for CD8) was associated with an improved outcome in several public breast cancer datasets.
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SHP099 and G12C-I each increased the expression of chemokine and cytokine genes that promote T cell recruitment (e.g., CXCL9-11; CCL5).
“SHP099 and G12C-I each increased the expression of chemokine and cytokine genes that promote T cell recruitment (e.g., CXCL9-11; CCL5; Araujo et al., 2018; Chow and Luster, 2014; Lavergne et al., 2004; Nagarsheth et al., 2017; Tokunaga et al., 2018)”
From SHP2 inhibition diminishes KRASG12C cycling and promotes tumor microenvironment remodeling (2021) · cites this paper as Araujo et al., 2018
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SHP2 inhibition diminishes KRASG12C cycling and promotes tumor microenvironment remodeling
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- Authors
- Araujo, J. M., Gomez, A. C., Aguilar, A., Salgado, R., Balko, J. M., Bravo, L., Doimi, F., Bretel, D., Morante, Z., Flores, C., Gomez, H. L., & Pinto, J. A.
- Affiliations
- Institut Jules Bordet (BE)
- Vanderbilt University (US)
- Universidad Privada San Juan Bautista (PE)
- Instituto Nacional de Enfermedades Neoplásicas (PE)
- ORCID
- Venue
- Scientific Reports
- Published
- 2018-03-20
- Volume
- 8
- Issue
- 1
- Pages
- 4899-4899
- ISSN
- 2045-2322 (ISSN-L)
- PMC
- PMC5861063
- OpenAlex
- W2805359975
- Cited by
- 108
- References
- 47
- Citations by year
- 2026: 12 · 2025: 14 · 2024: 10 · 2023: 14 · 2022: 12 · 2021: 21 · 2020: 10 · 2019: 13 · 2018: 2
- FWCI
- 3.48
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- Scientific Reports (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
- LA Referencia (Red Federada de Repositorios Institucionales de Publicaciones Científicas) (submittedVersion, cc-by)
- Greater South Information System
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cancer Research › Breast Cancer Treatment Studies
- Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Keywords
- triple-negative breast cancer, RANTES, tumor-infiltrating lymphocytes, immune cell recruitment, chemokines, CD8+ T cells, natural killer cells, macrophages, neoadjuvant chemotherapy, distant recurrence-free survival, CD8A, tumor immune microenvironment
- MeSH terms
- Adult, Aged, Cell Movement, Female, Humans, Killer Cells, Natural, Macrophages, Middle Aged, Peru, Retrospective Studies, Cohort Studies, Lymphocytes, Tumor-Infiltrating, CD8 Antigens, CD8-Positive T-Lymphocytes, Disease-Free Survival, Chemokine CCL5, Neoadjuvant Therapy, Tumor Burden, Young Adult, Triple Negative Breast Neoplasms
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