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Targeting Membrane Lipid a Potential Cancer Cure?

Cancer mortality and morbidity is projected to increase significantly over the next few decades. Current chemotherapeutic strategies have significant limitations, and there is great interest in seeking novel therapies which are capable of specifically targeting cancer cells. Given that fundamental d...

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Autores principales: Tan, Loh Teng-Hern, Chan, Kok-Gan, Pusparajah, Priyia, Lee, Wai-Leng, Chuah, Lay-Hong, Khan, Tahir Mehmood, Lee, Learn-Han, Goh, Bey-Hing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253362/
https://www.ncbi.nlm.nih.gov/pubmed/28167913
http://dx.doi.org/10.3389/fphar.2017.00012
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author Tan, Loh Teng-Hern
Chan, Kok-Gan
Pusparajah, Priyia
Lee, Wai-Leng
Chuah, Lay-Hong
Khan, Tahir Mehmood
Lee, Learn-Han
Goh, Bey-Hing
author_facet Tan, Loh Teng-Hern
Chan, Kok-Gan
Pusparajah, Priyia
Lee, Wai-Leng
Chuah, Lay-Hong
Khan, Tahir Mehmood
Lee, Learn-Han
Goh, Bey-Hing
author_sort Tan, Loh Teng-Hern
collection PubMed
description Cancer mortality and morbidity is projected to increase significantly over the next few decades. Current chemotherapeutic strategies have significant limitations, and there is great interest in seeking novel therapies which are capable of specifically targeting cancer cells. Given that fundamental differences exist between the cellular membranes of healthy cells and tumor cells, novel therapies based on targeting membrane lipids in cancer cells is a promising approach that deserves attention in the field of anticancer drug development. Phosphatidylethanolamine (PE), a lipid membrane component which exists only in the inner leaflet of cell membrane under normal circumstances, has increased surface representation on the outer membrane of tumor cells with disrupted membrane asymmetry. PE thus represents a potential chemotherapeutic target as the higher exposure of PE on the membrane surface of cancer cells. This feature as well as a high degree of expression of PE on endothelial cells in tumor vasculature, makes PE an attractive molecular target for future cancer interventions. There have already been several small molecules and membrane-active peptides identified which bind specifically to the PE molecules on the cancer cell membrane, subsequently inducing membrane disruption leading to cell lysis. This approach opens up a new front in the battle against cancer, and is of particular interest as it may be a strategy that may be prove effective against tumors that respond poorly to current chemotherapeutic agents. We aim to highlight the evidence suggesting that PE is a strong candidate to be explored as a potential molecular target for membrane targeted novel anticancer therapy.
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spelling pubmed-52533622017-02-06 Targeting Membrane Lipid a Potential Cancer Cure? Tan, Loh Teng-Hern Chan, Kok-Gan Pusparajah, Priyia Lee, Wai-Leng Chuah, Lay-Hong Khan, Tahir Mehmood Lee, Learn-Han Goh, Bey-Hing Front Pharmacol Pharmacology Cancer mortality and morbidity is projected to increase significantly over the next few decades. Current chemotherapeutic strategies have significant limitations, and there is great interest in seeking novel therapies which are capable of specifically targeting cancer cells. Given that fundamental differences exist between the cellular membranes of healthy cells and tumor cells, novel therapies based on targeting membrane lipids in cancer cells is a promising approach that deserves attention in the field of anticancer drug development. Phosphatidylethanolamine (PE), a lipid membrane component which exists only in the inner leaflet of cell membrane under normal circumstances, has increased surface representation on the outer membrane of tumor cells with disrupted membrane asymmetry. PE thus represents a potential chemotherapeutic target as the higher exposure of PE on the membrane surface of cancer cells. This feature as well as a high degree of expression of PE on endothelial cells in tumor vasculature, makes PE an attractive molecular target for future cancer interventions. There have already been several small molecules and membrane-active peptides identified which bind specifically to the PE molecules on the cancer cell membrane, subsequently inducing membrane disruption leading to cell lysis. This approach opens up a new front in the battle against cancer, and is of particular interest as it may be a strategy that may be prove effective against tumors that respond poorly to current chemotherapeutic agents. We aim to highlight the evidence suggesting that PE is a strong candidate to be explored as a potential molecular target for membrane targeted novel anticancer therapy. Frontiers Media S.A. 2017-01-23 /pmc/articles/PMC5253362/ /pubmed/28167913 http://dx.doi.org/10.3389/fphar.2017.00012 Text en Copyright © 2017 Tan, Chan, Pusparajah, Lee, Chuah, Khan, Lee and Goh. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Tan, Loh Teng-Hern
Chan, Kok-Gan
Pusparajah, Priyia
Lee, Wai-Leng
Chuah, Lay-Hong
Khan, Tahir Mehmood
Lee, Learn-Han
Goh, Bey-Hing
Targeting Membrane Lipid a Potential Cancer Cure?
title Targeting Membrane Lipid a Potential Cancer Cure?
title_full Targeting Membrane Lipid a Potential Cancer Cure?
title_fullStr Targeting Membrane Lipid a Potential Cancer Cure?
title_full_unstemmed Targeting Membrane Lipid a Potential Cancer Cure?
title_short Targeting Membrane Lipid a Potential Cancer Cure?
title_sort targeting membrane lipid a potential cancer cure?
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253362/
https://www.ncbi.nlm.nih.gov/pubmed/28167913
http://dx.doi.org/10.3389/fphar.2017.00012
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