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Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity

Many chemotherapeutic drugs have a narrow therapeutic window due to inefficient tumour cell permeation. Supramolecular self-associating amphiphilic salts (SSAs) are a unique class of small molecules that offer potential as next generation cancer drugs and/or therapeutic enhancement agents. Herein, w...

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Autores principales: Dora, Nova O., Blackburn, Edith, Boles, Jessica E., Williams, George T., White, Lisa J., Turner, Scarlett E. G., Hothersall, J. Daniel, Askwith, Trevor, Doolan, Jack A., Mulvihill, Daniel P., Garrett, Michelle D., Hiscock, Jennifer R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697675/
https://www.ncbi.nlm.nih.gov/pubmed/35423951
http://dx.doi.org/10.1039/d1ra02281d
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author Dora, Nova O.
Blackburn, Edith
Boles, Jessica E.
Williams, George T.
White, Lisa J.
Turner, Scarlett E. G.
Hothersall, J. Daniel
Askwith, Trevor
Doolan, Jack A.
Mulvihill, Daniel P.
Garrett, Michelle D.
Hiscock, Jennifer R.
author_facet Dora, Nova O.
Blackburn, Edith
Boles, Jessica E.
Williams, George T.
White, Lisa J.
Turner, Scarlett E. G.
Hothersall, J. Daniel
Askwith, Trevor
Doolan, Jack A.
Mulvihill, Daniel P.
Garrett, Michelle D.
Hiscock, Jennifer R.
author_sort Dora, Nova O.
collection PubMed
description Many chemotherapeutic drugs have a narrow therapeutic window due to inefficient tumour cell permeation. Supramolecular self-associating amphiphilic salts (SSAs) are a unique class of small molecules that offer potential as next generation cancer drugs and/or therapeutic enhancement agents. Herein, we demonstrate the cytotoxicity of seven SSAs towards both ovarian and glioblastoma cancer cells. We also utilize the intrinsic fluorescent properties of one of these lead SSAs to provide evidence for this class of compound to both bind to the exterior cancer cell surface and permeate the cell membrane, to become internalized. Furthermore, we demonstrate synergistic effects of two lead SSAs on cisplatin-mediated cytotoxicity of ovarian cancer cells and show that this correlates with increased DNA damage and apoptosis versus either agent alone. This work provides the first evidence that SSAs interact with and permeate cancer cell membranes and enhance the cytotoxic activity of a chemotherapeutic drug in human cancer cells.
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spelling pubmed-86976752022-04-13 Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity Dora, Nova O. Blackburn, Edith Boles, Jessica E. Williams, George T. White, Lisa J. Turner, Scarlett E. G. Hothersall, J. Daniel Askwith, Trevor Doolan, Jack A. Mulvihill, Daniel P. Garrett, Michelle D. Hiscock, Jennifer R. RSC Adv Chemistry Many chemotherapeutic drugs have a narrow therapeutic window due to inefficient tumour cell permeation. Supramolecular self-associating amphiphilic salts (SSAs) are a unique class of small molecules that offer potential as next generation cancer drugs and/or therapeutic enhancement agents. Herein, we demonstrate the cytotoxicity of seven SSAs towards both ovarian and glioblastoma cancer cells. We also utilize the intrinsic fluorescent properties of one of these lead SSAs to provide evidence for this class of compound to both bind to the exterior cancer cell surface and permeate the cell membrane, to become internalized. Furthermore, we demonstrate synergistic effects of two lead SSAs on cisplatin-mediated cytotoxicity of ovarian cancer cells and show that this correlates with increased DNA damage and apoptosis versus either agent alone. This work provides the first evidence that SSAs interact with and permeate cancer cell membranes and enhance the cytotoxic activity of a chemotherapeutic drug in human cancer cells. The Royal Society of Chemistry 2021-04-15 /pmc/articles/PMC8697675/ /pubmed/35423951 http://dx.doi.org/10.1039/d1ra02281d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Dora, Nova O.
Blackburn, Edith
Boles, Jessica E.
Williams, George T.
White, Lisa J.
Turner, Scarlett E. G.
Hothersall, J. Daniel
Askwith, Trevor
Doolan, Jack A.
Mulvihill, Daniel P.
Garrett, Michelle D.
Hiscock, Jennifer R.
Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity
title Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity
title_full Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity
title_fullStr Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity
title_full_unstemmed Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity
title_short Supramolecular self-associating amphiphiles (SSAs) as nanoscale enhancers of cisplatin anticancer activity
title_sort supramolecular self-associating amphiphiles (ssas) as nanoscale enhancers of cisplatin anticancer activity
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8697675/
https://www.ncbi.nlm.nih.gov/pubmed/35423951
http://dx.doi.org/10.1039/d1ra02281d
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