Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2022 Jul;14(4):e1792.
doi: 10.1002/wnan.1792. Epub 2022 Mar 22.

Bioinspired soft nanovesicles for site-selective cancer imaging and targeted therapies

Affiliations
Review

Bioinspired soft nanovesicles for site-selective cancer imaging and targeted therapies

Rajendra Prasad et al. Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2022 Jul.

Abstract

Cell-to-cell communication within the heterogeneous solid tumor environment plays a significant role in the uncontrolled metastasis of cancer. To inhibit the metastasis and growth of cancer cells, various chemically designed and biologically derived nanosized biomaterials have been applied for targeted cancer therapeutics applications. Over the years, bioinspired soft nanovesicles have gained tremendous attention for targeted cancer therapeutics due to their easy binding with tumor microenvironment, natural targeting ability, bio-responsive nature, better biocompatibility, high cargo capacity for multiple therapeutics agents, and long circulation time. These cell-derived nanovesicles guard their loaded cargo molecules from immune clearance and make them site-selective to cancer cells due to their natural binding and delivery abilities. Furthermore, bioinspired soft nanovesicles prevent cell-to-cell communication and secretion of cancer cell markers by delivering the therapeutics agents predominantly. Cell-derived vesicles, namely, exosomes, extracellular vesicles, and so forth have been recognized as versatile carriers for therapeutic biomolecules. However, low product yield, poor reproducibility, and uncontrolled particle size distribution have remained as major challenges of these soft nanovesicles. Furthermore, the surface biomarkers and molecular contents of these vesicles change with respect to the stage of disease and types. Here in this review, we have discussed numerous examples of bioinspired soft vesicles for targeted imaging and cancer therapeutic applications with their advantages and limitations. Importance of bioengineered soft nanovesicles for localized therapies with their clinical relevance has also been addressed in this article. Overall, cell-derived nanovesicles could be considered as clinically relevant platforms for cancer therapeutics. This article is categorized under: Biology-Inspired Nanomaterials > Nucleic Acid-Based Structures Therapeutic Approaches and Drug Discovery > Nanomedicine for Oncologic Disease.

Keywords: nanoCells; nanoTheranostics; nanovesicles; targeted therapy.

PubMed Disclaimer

Similar articles

Cited by

References

REFERENCES

    1. Abello, J., Nguyen, T. D. T., Marasini, R., Aryal, S., & Weiss, M. L. (2019). Biodistribution of gadolinium- and near infrared-labeled human umbilical cord mesenchymal stromal cell-derived exosomes in tumor bearing mice. Theranostics, 9(8), 2325-2345. https://doi.org/10.7150/thno.30030
    1. Ailuno, G., Baldassari, S., Lai, F., Florio, T., & Caviglioli, G. (2020). Exosomes and extracellular vesicles as emerging theranostic platforms in cancer research. Cell, 9(12), 2569.
    1. Al-Ahmady, Z., & Kostarelos, K. (2016). Chemical components for the design of temperature-responsive vesicles as cancer therapeutics. Chemical Reviews, 116(6), 3883-3918.
    1. Al-Nedawi, K., Meehan, B., Kerbel, R. S., Allison, A. C., & Rak, J. (2009). Endothelial expression of autocrine VEGF upon the uptake of tumor-derived microvesicles containing oncogenic EGFR. Proceedings of the National Academy of Sciences of the United States of America, 106(10), 3794-3799.
    1. Armstrong, J. P. K., Holme, M. N., & Stevens, M. M. (2017). Re-engineering extracellular vesicles as smart nanoscale therapeutics. ACS Nano, 11(1), 69-83.

Publication types

LinkOut - more resources