Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells

Chemotherapy-induced neurotoxicity can reduce the quality of life of patients by affecting their intelligence, senses and mobility. Ten percent of safety-related late-stage clinical failures are due to neurological side effects. Animal models are poor in predicting human neurotoxicity due to intersp...

Full description

Bibliographic Details
Main Authors: Ivanov, Delyan P., Al-Rubai, Abdal-jabbar, Grabowska, Anna M., Pratten, Margaret K.
Format: Article
Published: Elsevier 2016
Subjects:
Online Access:https://eprints.nottingham.ac.uk/37657/
_version_ 1848795505008574464
author Ivanov, Delyan P.
Al-Rubai, Abdal-jabbar
Grabowska, Anna M.
Pratten, Margaret K.
author_facet Ivanov, Delyan P.
Al-Rubai, Abdal-jabbar
Grabowska, Anna M.
Pratten, Margaret K.
author_sort Ivanov, Delyan P.
building Nottingham Research Data Repository
collection Online Access
description Chemotherapy-induced neurotoxicity can reduce the quality of life of patients by affecting their intelligence, senses and mobility. Ten percent of safety-related late-stage clinical failures are due to neurological side effects. Animal models are poor in predicting human neurotoxicity due to interspecies differences and most in vitro assays cannot distinguish neurotoxicity from general cytotoxicity for chemotherapeutics. We developed in vitro assays capable of quantifying the paediatric neurotoxic potential for cytotoxic drugs. Mixed cultures of human fetal brain cells were differentiated in monolayers and as 3D-neurospheres in the presence of non-neurotoxic chemotherapeutics (etoposide, teniposide) or neurotoxicants (methylmercury). The cytotoxic potency towards dividing progenitors versus differentiated neurons and astrocytes was compared using: (1) immunohistochemistry staining and cell counts in monolayers; (2) through quantitative Western blots in neurospheres; and (3) neurosphere migration assays. Etoposide and teniposide, were 5–10 times less toxic to differentiated neurons compared to the mix of all cells in monolayer cultures. In contrast, the neurotoxicant methylmercury did not exhibit selectivity and killed all cells with the same potency. In 3D neurospheres, etoposide and teniposide were 24 to 10 times less active against neurons compared to all cells. These assays can be used prioritise drugs for local drug delivery to brain tumours.
first_indexed 2025-11-14T19:33:09Z
format Article
id nottingham-37657
institution University of Nottingham Malaysia Campus
institution_category Local University
last_indexed 2025-11-14T19:33:09Z
publishDate 2016
publisher Elsevier
recordtype eprints
repository_type Digital Repository
spelling nottingham-376572020-05-04T18:18:42Z https://eprints.nottingham.ac.uk/37657/ Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells Ivanov, Delyan P. Al-Rubai, Abdal-jabbar Grabowska, Anna M. Pratten, Margaret K. Chemotherapy-induced neurotoxicity can reduce the quality of life of patients by affecting their intelligence, senses and mobility. Ten percent of safety-related late-stage clinical failures are due to neurological side effects. Animal models are poor in predicting human neurotoxicity due to interspecies differences and most in vitro assays cannot distinguish neurotoxicity from general cytotoxicity for chemotherapeutics. We developed in vitro assays capable of quantifying the paediatric neurotoxic potential for cytotoxic drugs. Mixed cultures of human fetal brain cells were differentiated in monolayers and as 3D-neurospheres in the presence of non-neurotoxic chemotherapeutics (etoposide, teniposide) or neurotoxicants (methylmercury). The cytotoxic potency towards dividing progenitors versus differentiated neurons and astrocytes was compared using: (1) immunohistochemistry staining and cell counts in monolayers; (2) through quantitative Western blots in neurospheres; and (3) neurosphere migration assays. Etoposide and teniposide, were 5–10 times less toxic to differentiated neurons compared to the mix of all cells in monolayer cultures. In contrast, the neurotoxicant methylmercury did not exhibit selectivity and killed all cells with the same potency. In 3D neurospheres, etoposide and teniposide were 24 to 10 times less active against neurons compared to all cells. These assays can be used prioritise drugs for local drug delivery to brain tumours. Elsevier 2016-12-01 Article PeerReviewed Ivanov, Delyan P., Al-Rubai, Abdal-jabbar, Grabowska, Anna M. and Pratten, Margaret K. (2016) Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells. Toxicology in Vitro, 37 . pp. 88-96. ISSN 1879-3177 Neural stem cell; preclinical screening model; in vitro neurotoxicity assay; neuronal differentiation; topoisomerase drugs; repurposing chemotherapeutics http://www.sciencedirect.com/science/article/pii/S0887233316301813 doi:10.1016/j.tiv.2016.09.007 doi:10.1016/j.tiv.2016.09.007
spellingShingle Neural stem cell; preclinical screening model; in vitro neurotoxicity assay; neuronal differentiation; topoisomerase drugs; repurposing chemotherapeutics
Ivanov, Delyan P.
Al-Rubai, Abdal-jabbar
Grabowska, Anna M.
Pratten, Margaret K.
Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
title Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
title_full Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
title_fullStr Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
title_full_unstemmed Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
title_short Separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
title_sort separating chemotherapy-related developmental neurotoxicity from cytotoxicity in monolayer and neurosphere cultures of human fetal brain cells
topic Neural stem cell; preclinical screening model; in vitro neurotoxicity assay; neuronal differentiation; topoisomerase drugs; repurposing chemotherapeutics
url https://eprints.nottingham.ac.uk/37657/
https://eprints.nottingham.ac.uk/37657/
https://eprints.nottingham.ac.uk/37657/