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Breast Cancer Treatment Strategies Targeting the Tumor Microenvironment: How to Convert "Cold" Tumors to "Hot" Tumors

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 Jul 13
PMID 39000314
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Abstract

Breast cancer characterized as "cold tumors" exhibit low levels of immune cell infiltration, which limits the efficacy of conventional immunotherapy. Recent studies have focused on strategies using nanotechnology combined with tumor microenvironment modulation to transform "cold tumors" into "hot tumors". This approach involves the use of functionalized nanoparticles that target and modify the tumor microenvironment to promote the infiltration and activation of antitumor immune cells. By delivering immune activators or blocking immunosuppressive signals, these nanoparticles activate otherwise dormant immune responses, enhancing tumor immunogenicity and the therapeutic response. These strategies not only promise to increase the response rate of breast cancer patients to existing immunotherapies but also may pave new therapeutic avenues, providing a new direction for the immunotherapy of breast cancer.

Citing Articles

Real‑world evaluation of the efficacy of immune checkpoint inhibitors in the treatment of metastatic breast cancer.

Qian X, Tao Y, Chen H, Li X, Wang Y, Xu X Oncol Lett. 2024; 29(1):29.

PMID: 39512498 PMC: 11542155. DOI: 10.3892/ol.2024.14775.

References
1.
Erra Diaz F, Dantas E, Geffner J . Unravelling the Interplay between Extracellular Acidosis and Immune Cells. Mediators Inflamm. 2019; 2018:1218297. PMC: 6332927. DOI: 10.1155/2018/1218297. View

2.
Reeves A, Vinogradov S, Morrissey P, Chernin M, Ahmed M . Curcumin-encapsulating Nanogels as an Effective Anticancer Formulation for Intracellular Uptake. Mol Cell Pharmacol. 2016; 7(3):25-40. PMC: 4770584. DOI: 10.4255/mcpharmacol.15.04. View

3.
Cun X, Chen J, Li M, He X, Tang X, Guo R . Tumor-Associated Fibroblast-Targeted Regulation and Deep Tumor Delivery of Chemotherapeutic Drugs with a Multifunctional Size-Switchable Nanoparticle. ACS Appl Mater Interfaces. 2019; 11(43):39545-39559. DOI: 10.1021/acsami.9b13957. View

4.
Fu W, Lei C, Yu Y, Liu S, Li T, Lin F . EGFR/Notch Antagonists Enhance the Response to Inhibitors of the PI3K-Akt Pathway by Decreasing Tumor-Initiating Cell Frequency. Clin Cancer Res. 2019; 25(9):2835-2847. DOI: 10.1158/1078-0432.CCR-18-2732. View

5.
van Goethem E, Poincloux R, Gauffre F, Maridonneau-Parini I, Le Cabec V . Matrix architecture dictates three-dimensional migration modes of human macrophages: differential involvement of proteases and podosome-like structures. J Immunol. 2009; 184(2):1049-61. DOI: 10.4049/jimmunol.0902223. View