Cargando…

Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types

BACKGROUND: Monepantel is an anti‐helminthic drug that also has anti‐cancer properties. Despite several studies over the years, the molecular target of monepantel in mammalian cells is still unknown, and its mechanism‐of‐action is not fully understood, though effects on cell cycle, mTOR signalling a...

Descripción completa

Detalles Bibliográficos
Autores principales: Harris, Tiffany J., Liao, Yang, Shi, Wei, Evangelista, Marco, Pal, Bhupinder, Puthalakath, Hamsa, Aston, Roger, Mollard, Richard, Mariadason, John M., Lee, Erinna F., Fairlie, Walter D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315739/
https://www.ncbi.nlm.nih.gov/pubmed/37148543
http://dx.doi.org/10.1002/cam4.6021
_version_ 1785067562172678144
author Harris, Tiffany J.
Liao, Yang
Shi, Wei
Evangelista, Marco
Pal, Bhupinder
Puthalakath, Hamsa
Aston, Roger
Mollard, Richard
Mariadason, John M.
Lee, Erinna F.
Fairlie, Walter D.
author_facet Harris, Tiffany J.
Liao, Yang
Shi, Wei
Evangelista, Marco
Pal, Bhupinder
Puthalakath, Hamsa
Aston, Roger
Mollard, Richard
Mariadason, John M.
Lee, Erinna F.
Fairlie, Walter D.
author_sort Harris, Tiffany J.
collection PubMed
description BACKGROUND: Monepantel is an anti‐helminthic drug that also has anti‐cancer properties. Despite several studies over the years, the molecular target of monepantel in mammalian cells is still unknown, and its mechanism‐of‐action is not fully understood, though effects on cell cycle, mTOR signalling and autophagy have been implicated. METHODS: Viability assays were performed on >20 solid cancer cell cells, and apoptosis assays were performed on a subset of these, including 3D cultures. Genetic deletion of BAX/BAK and ATG were used to establish roles of apoptosis and autophagy in killing activity. RNA‐sequencing was performed on four cell lines after monepantel treatment, and differentially regulated genes were confirmed by Western blotting. RESULTS: We showed that monepantel has anti‐proliferative activity on a broad range of cancer cell lines. In some, this was associated with induction of apoptosis which was confirmed using a BAX/BAK‐deficient cell line. However, proliferation is still inhibited in these cells following monepantel treatment, indicating cell‐cycle disruption as the major anti‐cancer effect. Previous studies have also indicated autophagic cell death occurs following monepantel treatment. We showed autophagy induction in multiple cell lines; however, deletion of a key autophagy regulator ATG7 had minimal impact on monepantel’s anti‐proliferative activity, suggesting autophagy is associated with, but not required for its anti‐tumour effects. Transcriptomic analysis of four cell lines treated with monepantel revealed downregulation of many genes involved in the cell cycle, and upregulation of genes linked to ATF4‐mediated ER stress responses, especially those involved in amino‐acid metabolism and protein synthesis. CONCLUSIONS: As these outcomes are all associated with mTOR signalling, cell cycle and autophagy, we now provide a likely triggering mechanism for the anti‐cancer activity of monepantel.
format Online
Article
Text
id pubmed-10315739
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-103157392023-07-04 Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types Harris, Tiffany J. Liao, Yang Shi, Wei Evangelista, Marco Pal, Bhupinder Puthalakath, Hamsa Aston, Roger Mollard, Richard Mariadason, John M. Lee, Erinna F. Fairlie, Walter D. Cancer Med RESEARCH ARTICLES BACKGROUND: Monepantel is an anti‐helminthic drug that also has anti‐cancer properties. Despite several studies over the years, the molecular target of monepantel in mammalian cells is still unknown, and its mechanism‐of‐action is not fully understood, though effects on cell cycle, mTOR signalling and autophagy have been implicated. METHODS: Viability assays were performed on >20 solid cancer cell cells, and apoptosis assays were performed on a subset of these, including 3D cultures. Genetic deletion of BAX/BAK and ATG were used to establish roles of apoptosis and autophagy in killing activity. RNA‐sequencing was performed on four cell lines after monepantel treatment, and differentially regulated genes were confirmed by Western blotting. RESULTS: We showed that monepantel has anti‐proliferative activity on a broad range of cancer cell lines. In some, this was associated with induction of apoptosis which was confirmed using a BAX/BAK‐deficient cell line. However, proliferation is still inhibited in these cells following monepantel treatment, indicating cell‐cycle disruption as the major anti‐cancer effect. Previous studies have also indicated autophagic cell death occurs following monepantel treatment. We showed autophagy induction in multiple cell lines; however, deletion of a key autophagy regulator ATG7 had minimal impact on monepantel’s anti‐proliferative activity, suggesting autophagy is associated with, but not required for its anti‐tumour effects. Transcriptomic analysis of four cell lines treated with monepantel revealed downregulation of many genes involved in the cell cycle, and upregulation of genes linked to ATF4‐mediated ER stress responses, especially those involved in amino‐acid metabolism and protein synthesis. CONCLUSIONS: As these outcomes are all associated with mTOR signalling, cell cycle and autophagy, we now provide a likely triggering mechanism for the anti‐cancer activity of monepantel. John Wiley and Sons Inc. 2023-05-06 /pmc/articles/PMC10315739/ /pubmed/37148543 http://dx.doi.org/10.1002/cam4.6021 Text en © 2023 The Authors. Cancer Medicine published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle RESEARCH ARTICLES
Harris, Tiffany J.
Liao, Yang
Shi, Wei
Evangelista, Marco
Pal, Bhupinder
Puthalakath, Hamsa
Aston, Roger
Mollard, Richard
Mariadason, John M.
Lee, Erinna F.
Fairlie, Walter D.
Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
title Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
title_full Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
title_fullStr Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
title_full_unstemmed Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
title_short Induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
title_sort induction of endoplasmic reticulum stress is associated with the anti‐tumor activity of monepantel across cancer types
topic RESEARCH ARTICLES
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10315739/
https://www.ncbi.nlm.nih.gov/pubmed/37148543
http://dx.doi.org/10.1002/cam4.6021
work_keys_str_mv AT harristiffanyj inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT liaoyang inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT shiwei inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT evangelistamarco inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT palbhupinder inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT puthalakathhamsa inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT astonroger inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT mollardrichard inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT mariadasonjohnm inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT leeerinnaf inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes
AT fairliewalterd inductionofendoplasmicreticulumstressisassociatedwiththeantitumoractivityofmonepantelacrosscancertypes