University of Sussex
Browse
fnano-02-00001.pdf (694.33 kB)

Status and future directions of anti-metastatic cancer nanomedicines for the inhibition of cathepsin L

Download (694.33 kB)
journal contribution
posted on 2023-06-07, 07:02 authored by Tanveer A Tabish, Md Zahidul I Pranjol, Jacqueline L Whatmore, Shaowei Zhang
Angiogenesis, tissue invasion and metastasis in the tumour microenvironment are all critical hallmarks of cancer. Upregulation of cathepsin L plays an important role in angiogenesis and metastasis through its ability to degrade the extracellular matrix, facilitating tissue remodeling and tumour cell invasion. Thus, cathepsin L is a potential therapeutic target for anticancer nanomedicine, with its inhibition emerging as an innovative and potentially promising therapeutic intervention for the development of anti-invasion and anti-metastatic enzyme therapies. Nanotechnology-based platforms have been extensively tested in the anti-cancer nanomedicine field with effective anti-tumour efficacy. These nanodrugs can suppress tumour cell proliferation, thereby reducing tumour growth. Recently, nanomedicinal approaches have also emerged as effective anti-metastatic strategies, including the use of graphene oxide and gold nanoparticles. With a focus on recent advances in developing nanotechnology to inhibit cathepsin L, this review provides an in-depth examination of this stimulating field in the context of tumour microenvironments. Innovative anti-metastatic agents may lead to new options for the treatment of cancers.

History

Publication status

  • Published

File Version

  • Published version

Journal

Frontiers in Nanotechnology

ISSN

2673-3013

Publisher

Frontiers

Issue

a1

Volume

2

Page range

1-10

Department affiliated with

  • Biochemistry Publications

Full text available

  • Yes

Peer reviewed?

  • Yes

Legacy Posted Date

2020-05-19

First Open Access (FOA) Date

2020-05-19

First Compliant Deposit (FCD) Date

2020-05-18

Usage metrics

    University of Sussex (Publications)

    Categories

    No categories selected

    Licence

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC