Towards a More Efficient Breast Cancer Therapy Using Active Human Cell Membrane-Coated Metal–Organic Frameworks

Author:

Graván Pablo123456ORCID,Rojas Sara7ORCID,Picchi Darina Francesca89ORCID,Galisteo-González Francisco1,Horcajada Patricia8ORCID,Marchal Juan Antonio23456ORCID

Affiliation:

1. Department of Applied Physics, Faculty of Science, University of Granada, 18071 Granada, Spain

2. Department of Human Anatomy and Embryology, Faculty of Medicine, University of Granada, 18016 Granada, Spain

3. Instituto de Investigación Biosanitaria de Granada (ibs. GRANADA), 18012 Granada, Spain

4. Biopathology and Regenerative Medicine Institute (IBIMER), Centre for Biomedical Research (CIBM), University of Granada, 18016 Granada, Spain

5. Excellence Research Unit Modelling Nature (MNat), University of Granada, 18016 Granada, Spain

6. BioFab i3D—Biofabrication and 3D (Bio)Printing Laboratory, University of Granada, 18100 Granada, Spain

7. Department of Inorganic Chemistry, Faculty of Science, University of Granada, Av. Fuentenueva s/n, 18071 Granada, Spain

8. Advanced Porous Materials Unit, IMDEA Energy Institute, Av. Ramón de la Sagra 3, 28935 Móstoles, Spain

9. Escuela Internacional de Doctorado, Universidad Rey Juan Carlos, c/Tulipan, s/n, Móstoles, 28933 Madrid, Spain

Abstract

The recent description of well-defined molecular subtypes of breast cancer has led to the clinical development of a number of successful molecular targets. Particularly, triple-negative breast cancer (TNBC) is an aggressive type of breast cancer with historically poor outcomes, mainly due to the lack of effective targeted therapies. Recent progresses in materials science have demonstrated the impressive properties of metal–organic framework nanoparticles (NPs) as antitumoral drug delivery systems. Here, in a way to achieve efficient bio-interfaces with cancer cells and improve their internalization, benchmarked MIL-100(Fe) NPs were coated with cell membranes (CMs) derived from the human TNBC cell line MDA-MB-468. The prepared CMs-coated metal–organic framework (CMs_MIL-100(Fe)) showed enhanced colloidal stability, cellular uptake, and cytotoxicity in MDA-MB-468 cells compared to non-coated NPs, paving the way for these human CMs-coated MIL-100(Fe) NPs as effective targeted therapies against the challenging TNBC.

Funder

Universidad de Granada

Publisher

MDPI AG

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