PLGA–Nano-Encapsulated Disulfiram Inhibits Hypoxia-Induced NF-κB, Cancer Stem Cells, and Targets Glioblastoma In Vitro and In Vivo

Kannappan, Vinodh, Liu, Ying, Wang, Zhipeng, Azar, Karim, Kurusamy, Sathishkumar, Kilari, Rajagopal S, Armesilla, Angel L, Morris, Mark R, Najlah, Mohammad, Liu, Peng, Bian, Xiu-Wu and Wang, Weiguang (2022) PLGA–Nano-Encapsulated Disulfiram Inhibits Hypoxia-Induced NF-κB, Cancer Stem Cells, and Targets Glioblastoma In Vitro and In Vivo. Molecular Cancer Therapeutics, 21 (8). pp. 1273-1284. ISSN 1538-8514

[img] Text
Accepted Version
Restricted to Repository staff only until 17 May 2023.
Available under the following license: Creative Commons Attribution Non-commercial No Derivatives.

Download (6MB) | Request a copy
Official URL: https://aacrjournals.org/mct/article-abstract/21/8...

Abstract

Glioblastoma stem cell (GSC) is the major cause of glioblastoma multiforme (GBM) chemotherapy failure. Hypoxia is one of the determinants of GSC. NF-κB plays a pivotal link between hypoxia and cancer stem cells (CSCs). Disulfiram, an antialcoholism drug, has very strong NF-κB–inhibiting and anti-CSC activity. In this study, the in vitro anti-GSC activity of disulfiram and in vivo anti-GBM efficacy of poly lactic–co-glycolic acid nanoparticle-encapsulated disulfiram (DS-PLGA) were examined. We attempt to elucidate the molecular network between hypoxia and GSCs and also examined the anti-GSC activity of disulfiram in vitro and in vivo. The influence of GSCs and hypoxia on GBM chemoresistance and invasiveness was studied in hypoxic and spheroid cultures. The molecular regulatory roles of NF-κB, hypoxia-inducible factor-1α (HIF1α), and HIF2α were investigated using stably transfected U373MG cell lines. The hypoxia in neurospheres determines the cancer stem cell characteristics of the sphere-cultured GBM cell lines (U87MG, U251MG, U373MG). NF-κB is located at a higher hierarchical position than HIF1α/HIF2α in hypoxic regulatory network and plays a key role in hypoxia-induced GSC characters. DS inhibits NF-κB activity and targets hypoxia-induced GSCs. It showed selective toxicity to GBM cells, eradicates GSCs, and blocks migration and invasion at very low concentrations. DS-PLGA efficaciously inhibits orthotopic and subcutaneous U87MG xenograft in mouse models with no toxicity to vital organs.

Item Type: Journal Article
Keywords: Cell Line, Tumor, Animals, Humans, Mice, Glioblastoma, Brain Neoplasms, Disulfiram, NF-kappa B, Neoplastic Stem Cells, Hypoxia
Faculty: Faculty of Health, Education, Medicine & Social Care
SWORD Depositor: Symplectic User
Depositing User: Symplectic User
Date Deposited: 25 Aug 2022 13:34
Last Modified: 25 Aug 2022 13:34
URI: https://arro.anglia.ac.uk/id/eprint/707865

Actions (login required)

Edit Item Edit Item