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Published on: February 9, 2019
Targeting Membrane Lipid a Potential Cancer Cure?
Loh Teng-Hern Tan1, Kok-Gan Chan2, Priyia Pusparajah3
1Novel Bacteria and Drug Discovery Research Group, School of Pharmacy, Monash University Malaysia Bandar Sunway, Malaysia.
Abstract:
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.
Insights
Phosphatidylethanolamine (PE), a membrane lipid, shows increased surface presence on cancer cells. Targeting PE offers a novel therapeutic strategy for cancer, potentially overcoming resistance to conventional treatments.
Area of Science:
- Oncology
- Molecular Biology
- Biochemistry
Background:
- Cancer mortality is rising, necessitating novel therapeutic strategies.
- Current chemotherapies have limitations and significant side effects.
- Targeting cancer-specific cellular membrane differences is a promising approach.
Purpose of the Study:
- To highlight phosphatidylethanolamine (PE) as a potential molecular target for novel anticancer therapies.
- To explore the potential of targeting membrane lipids in cancer drug development.
- To investigate PE's role in cancer cell membrane disruption.
Main Methods:
- Review of existing literature on PE expression in cancer cells.
- Analysis of small molecules and peptides targeting PE.
- Evaluation of PE's presence on tumor vasculature endothelial cells.
Main Results:
- Phosphatidylethanolamine (PE) is uniquely exposed on the outer membrane of cancer cells due to disrupted asymmetry.
- PE is also highly expressed on tumor vasculature endothelial cells.
- Several agents have been identified that bind PE, induce membrane disruption, and cause cancer cell lysis.
Conclusions:
- PE represents a viable molecular target for developing novel, membrane-centric anticancer therapies.
- Targeting PE may offer an effective strategy against chemo-resistant tumors.
- Further exploration of PE-targeted therapies is warranted in anticancer drug development.
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