» Articles » PMID: 37108371

Extracellular Vesicles in Breast Cancer: From Biology and Function to Clinical Diagnosis and Therapeutic Management

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2023 Apr 28
PMID 37108371
Authors
Affiliations
Soon will be listed here.
Abstract

Breast cancer (BC) is the first worldwide most frequent cancer in both sexes and the most commonly diagnosed in females. Although BC mortality has been thoroughly declining over the past decades, there are still considerable differences between women diagnosed with early BC and when metastatic BC is diagnosed. BC treatment choice is widely dependent on precise histological and molecular characterization. However, recurrence or distant metastasis still occurs even with the most recent efficient therapies. Thus, a better understanding of the different factors underlying tumor escape is mainly mandatory. Among the leading candidates is the continuous interplay between tumor cells and their microenvironment, where extracellular vesicles play a significant role. Among extracellular vesicles, smaller ones, also called exosomes, can carry biomolecules, such as lipids, proteins, and nucleic acids, and generate signal transmission through an intercellular transfer of their content. This mechanism allows tumor cells to recruit and modify the adjacent and systemic microenvironment to support further invasion and dissemination. By reciprocity, stromal cells can also use exosomes to profoundly modify tumor cell behavior. This review intends to cover the most recent literature on the role of extracellular vesicle production in normal and cancerous breast tissues. Specific attention is paid to the use of extracellular vesicles for early BC diagnosis, follow-up, and prognosis because exosomes are actually under the spotlight of researchers as a high-potential source of liquid biopsies. Extracellular vesicles in BC treatment as new targets for therapy or efficient nanovectors to drive drug delivery are also summarized.

Citing Articles

Invasion and metastasis in cancer: molecular insights and therapeutic targets.

Li Y, Liu F, Cai Q, Deng L, OuYang Q, Zhang X Signal Transduct Target Ther. 2025; 10(1):57.

PMID: 39979279 PMC: 11842613. DOI: 10.1038/s41392-025-02148-4.


Synergistic therapeutic effects of pertuzumab and pyrrolitinib in HER-2-positive breast cancer: modulation of the PI3K/AKT pathway.

Zhu X, Xu Y, Zheng X, Li Y Am J Cancer Res. 2025; 15(1):141-152.

PMID: 39949924 PMC: 11815364. DOI: 10.62347/COSC7070.


Who is Focusing on Women's Health: A Bibliometric Analysis of Global Research Trends on Overweight in Female Patients with Gynecologic or Breast Cancer.

Gu J, Zhang H, Qian K, Ye X, Wu G Int J Womens Health. 2024; 16:2157-2171.

PMID: 39713093 PMC: 11662632. DOI: 10.2147/IJWH.S496718.


Exosomes and breast cancer angiogenesis; Highlights in intercellular communication.

Khanicheragh P, Abbasi-Malati Z, Saghebasl S, Hassanpour P, Milani S, Rahbarghazi R Cancer Cell Int. 2024; 24(1):402.

PMID: 39696346 PMC: 11656829. DOI: 10.1186/s12935-024-03606-9.


Advancements in Exosome Proteins for Breast Cancer Diagnosis and Detection: With a Focus on Nanotechnology.

Saadh M, Al-Rihaymee A, Kaur M, Kumar A, Mutee A, Ismaeel G AAPS PharmSciTech. 2024; 25(8):276.

PMID: 39604642 DOI: 10.1208/s12249-024-02983-8.


References
1.
Kumar A, Deep G . Hypoxia in tumor microenvironment regulates exosome biogenesis: Molecular mechanisms and translational opportunities. Cancer Lett. 2020; 479:23-30. DOI: 10.1016/j.canlet.2020.03.017. View

2.
Kim M, Kim D, Jung W, Koo J . Expression of metabolism-related proteins in triple-negative breast cancer. Int J Clin Exp Pathol. 2014; 7(1):301-12. PMC: 3885485. View

3.
Holdenrieder S, Stieber P . Therapy control in oncology by circulating nucleosomes. Ann N Y Acad Sci. 2004; 1022:211-6. DOI: 10.1196/annals.1318.032. View

4.
Twafra S, Sokolik C, Sneh T, Srikanth K, Meirson T, Genna A . A novel Pyk2-derived peptide inhibits invadopodia-mediated breast cancer metastasis. Oncogene. 2022; 42(4):278-292. DOI: 10.1038/s41388-022-02481-w. View

5.
Takahashi Y, Nishikawa M, Shinotsuka H, Matsui Y, Ohara S, Imai T . Visualization and in vivo tracking of the exosomes of murine melanoma B16-BL6 cells in mice after intravenous injection. J Biotechnol. 2013; 165(2):77-84. DOI: 10.1016/j.jbiotec.2013.03.013. View