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CCL20 is a Potential Therapeutic Target Associated with Immune Infiltration in Breast Cancer

Overview
Journal J Int Med Res
Publisher Sage Publications
Specialty General Medicine
Date 2023 Aug 12
PMID 37571985
Authors
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Abstract

Objectives: CCL20 is a chemotactic factor that is involved in immune cell recruitment and cancer progression. However, the role of CCL20 in the prognosis of breast cancer remains unclear. This study analyzed correlations between CCL20 expression and immune infiltration, clinicopathological parameters, and prognosis in breast cancer patients.

Methods: Correlations between CCL20 expression and clinicopathological parameters, prognosis, and immune infiltration in breast cancer were determined using the TIMER, UALCAN, and PrognoScan databases. Furthermore, gene-gene and protein-protein interactions were determined using GeneMANIA and STING network construction, respectively.

Results: CCL20 expression was significantly upregulated in breast cancer and had significant associations with clinicopathological features, including race, sex, age, menopause status, cancer stage, cancer subclass, and nodal metastasis; moreover, patients with higher CCL20 expression exhibited poor prognosis. Meanwhile, CCL20 expression was significantly correlated with the infiltration of immune cells in breast cancer, including monocytes, neutrophils, tumor-associated macrophages, Th1 cells, regulatory T cells, and exhausted T cells. Moreover, the network of CCL20 expression showed the majority genes and proteins were associated with immune reactions.

Conclusions: CCL20 is a prognosis-related biomarker in breast cancer on the basis of its correlation with immune infiltration levels and has potential to also be a therapeutic target.

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References
1.
Zhang R, Yang Y, Dong W, Lin M, He J, Zhang X . D-mannose facilitates immunotherapy and radiotherapy of triple-negative breast cancer via degradation of PD-L1. Proc Natl Acad Sci U S A. 2022; 119(8). PMC: 8872783. DOI: 10.1073/pnas.2114851119. View

2.
Liu Y, Lagowski J, Gao S, Raymond J, White C, Kulesz-Martin M . Regulation of the psoriatic chemokine CCL20 by E3 ligases Trim32 and Piasy in keratinocytes. J Invest Dermatol. 2010; 130(5):1384-90. PMC: 2898505. DOI: 10.1038/jid.2009.416. View

3.
Muscella A, Vetrugno C, Marsigliante S . CCL20 promotes migration and invasiveness of human cancerous breast epithelial cells in primary culture. Mol Carcinog. 2017; 56(11):2461-2473. DOI: 10.1002/mc.22693. View

4.
Kitamura T, Pollard J . Therapeutic potential of chemokine signal inhibition for metastatic breast cancer. Pharmacol Res. 2015; 100:266-70. PMC: 4617477. DOI: 10.1016/j.phrs.2015.08.004. View

5.
Shen M, Smith H, Wei Y, Jiang Y, Zhao S, Wang N . Pharmacological disruption of the MTDH-SND1 complex enhances tumor antigen presentation and synergizes with anti-PD-1 therapy in metastatic breast cancer. Nat Cancer. 2022; 3(1):60-74. PMC: 8818088. DOI: 10.1038/s43018-021-00280-y. View