» Articles » PMID: 32481745

Cdc42-Dependent Transfer of Mir301 from Breast Cancer-Derived Extracellular Vesicles Regulates the Matrix Modulating Ability of Astrocytes at the Blood-Brain Barrier

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2020 Jun 3
PMID 32481745
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Breast cancer brain metastasis is a major clinical challenge and is associated with a dismal prognosis. Understanding the mechanisms underlying the early stages of brain metastasis can provide opportunities to develop efficient diagnostics and therapeutics for this significant clinical challenge. We have previously reported that breast cancer-derived extracellular vesicles (EVs) breach the blood-brain barrier (BBB) via transcytosis and can promote brain metastasis. Here, we elucidate the functional consequences of EV transport across the BBB. We demonstrate that brain metastasis-promoting EVs can be internalized by astrocytes and modulate the behavior of these cells to promote extracellular matrix remodeling in vivo. We have identified protein and miRNA signatures in these EVs that can lead to the interaction of EVs with astrocytes and, as such, have the potential to serve as targets for development of diagnostics and therapeutics for early detection and therapeutic intervention in breast cancer brain metastasis.

Citing Articles

AZIN1 level is increased in medulloblastoma and correlates with c-Myc activity and tumor phenotype.

Sesen J, Martinez T, Busatto S, Poluben L, Nassour H, Stone C J Exp Clin Cancer Res. 2025; 44(1):56.

PMID: 39962590 PMC: 11831846. DOI: 10.1186/s13046-025-03274-1.


Breast Cancer-Derived Extracellular Vesicles Modulate the Cytoplasmic and Cytoskeletal Dynamics of Blood-Brain Barrier Endothelial Cells.

Busatto S, Song T, Kim H, Hallinan C, Lombardo M, Stemmer-Rachamimov A J Extracell Vesicles. 2025; 14(1):e70038.

PMID: 39868462 PMC: 11770372. DOI: 10.1002/jev2.70038.


Extracellular vesicle-mediated pre-metastatic niche formation via altering host microenvironments.

Li Y, Zheng Y, Tan X, Du Y, Wei Y, Liu S Front Immunol. 2024; 15:1367373.

PMID: 38495881 PMC: 10940351. DOI: 10.3389/fimmu.2024.1367373.


The role of microRNAs in brain metastasis.

Hudson K, Mondia M, Zhang Y, Saha S, Gibert Jr M, Dube C J Neurooncol. 2024; 166(2):231-241.

PMID: 38194195 PMC: 10834572. DOI: 10.1007/s11060-023-04541-x.


Extracellular vesicles in the breast cancer brain metastasis: physiological functions and clinical applications.

Sakamoto Y, Ochiya T, Yoshioka Y Front Hum Neurosci. 2023; 17:1278501.

PMID: 38111675 PMC: 10725966. DOI: 10.3389/fnhum.2023.1278501.


References
1.
Cagney D, Martin A, Catalano P, Redig A, Lin N, Lee E . Incidence and prognosis of patients with brain metastases at diagnosis of systemic malignancy: a population-based study. Neuro Oncol. 2017; 19(11):1511-1521. PMC: 5737512. DOI: 10.1093/neuonc/nox077. View

2.
Pathan M, Keerthikumar S, Chisanga D, Alessandro R, Ang C, Askenase P . A novel community driven software for functional enrichment analysis of extracellular vesicles data. J Extracell Vesicles. 2017; 6(1):1321455. PMC: 5505018. DOI: 10.1080/20013078.2017.1321455. View

3.
Fernandez C, Butterfield C, Jackson G, Moses M . Structural and functional uncoupling of the enzymatic and angiogenic inhibitory activities of tissue inhibitor of metalloproteinase-2 (TIMP-2): loop 6 is a novel angiogenesis inhibitor. J Biol Chem. 2003; 278(42):40989-95. DOI: 10.1074/jbc.M306176200. View

4.
Mulcahy L, Pink R, Carter D . Routes and mechanisms of extracellular vesicle uptake. J Extracell Vesicles. 2014; 3. PMC: 4122821. DOI: 10.3402/jev.v3.24641. View

5.
Morad G, Carman C, Hagedorn E, Perlin J, Zon L, Mustafaoglu N . Tumor-Derived Extracellular Vesicles Breach the Intact Blood-Brain Barrier Transcytosis. ACS Nano. 2019; 13(12):13853-13865. PMC: 7169949. DOI: 10.1021/acsnano.9b04397. View