New Method Sneaks Drugs into Cancer Cells Before Triggering Release
News May 13, 2014
The method can be likened to keeping a cancer-killing bomb and its detonator separate until they are inside a cancer cell, where they then combine to destroy the cell.
“This is an efficient, fast-acting way of delivering drugs to cancer cells and triggering cell death,” says Dr. Ran Mo, lead author of a paper on the work and a postdoctoral researcher in the joint biomedical engineering program at North Carolina State University and the University of North Carolina at Chapel Hill. “We also used lipid-based nanocapsules that are already in use for clinical applications, making it closer to use in the real world.”
The technique uses nanoscale lipid-based capsules, or liposomes, to deliver both the drug and the release mechanism into cancer cells. One set of liposomes contains adenosine-5’-triphosphate (ATP), the so-called “energy molecule.” A second set of liposomes contains an anti-cancer drug called doxorubicin (Dox) that is embedded in a complex of DNA molecules. When the DNA molecules come into contact with high levels of ATP, they unfold and release the Dox. The surface of the liposomes is integrated with positively charged lipids or peptides, which act as corkscrews to introduce the liposomes into cancer cells.
As the liposomes are absorbed into a cancer cell, they are sealed off from the rest of the cell in an endosome – a compartment that walls off all foreign material that gets into a cell.
The environment inside an endosome is acidic, which causes the Dox liposomes and ATP liposomes to fuse together, as well as to the wall of the endosome itself.
Meanwhile, two other things are happening simultaneously. First, the ATP liposomes spill their ATP into the Dox liposomes, releasing the Dox from its DNA cage. Second, the walls of the Dox liposomes create an opening in the endosome, spilling their Dox-rich contents into the surrounding cell – leading to cell death.
In a mouse model, the researchers found that the new technique significantly decreased the size of breast cancer tumors compared to treatment that used Dox without the nanoscale liposomes.
“This work is somewhat similar to previous research we’ve done with polymer-based nanogels – but there is a key difference,” says Dr. Zhen Gu, senior author of the paper and an assistant professor in the joint biomedical engineering program. “The difference is that this liposome-based technique allows us to introduce additional ATP into the cancer cell, releasing the drug more quickly.
“Being able to adjust ATP levels is important because some cancer cells are ATP deficient,” Gu adds. “But this technique would work even in those environments.”
The paper, “Enhanced Anticancer Efficacy by ATP-Mediated Liposomal Drug Delivery,” is published online in Angewandte Chemie. The paper was co-authored by Tianyue Jiang, a Ph.D. student in the joint biomedical engineering program. The research was supported by the National Institutes of Health under grant 1UL1TR001111 and funding from NC State and UNC-Chapel Hill.
A new study has identified a drug that potentially could make a common type of immunotherapy for cancer even more effective. The study in laboratory mice found that the drug dasatinib, which is FDA-approved to treat certain types of leukemia, greatly enhances responses to a form of immunotherapy that is used against a wide range of other cancers.
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