A group of researchers from the University of Toronto and the Hospital for Sick Childrenhave developed a new wayto deliver molecules that target specific genes within cells. The platform, which uses a modified form of diphtheria toxin, has been shown to downregulate critical genes in cancer cells, and could be used for other genetic diseases as well.
The team, led by University ProfessorMolly Shoichet of the Faculty of Applied Science & Engineeringand Roman Melnyk, anassociateprofessorthe department of biochemistry in the Faculty of Medicine and a senior scientist at SickKids, found inspiration from an unexpected source: diphtheria toxin.
The research was published recently in the journal Science Advances.
Scientists looking to place molecules inside cells have a number of existing tools to choose from, but most suffer from the same drawback: while the molecule gets inside the cell, it remains trapped in a kind of bubble called an endosome. If the goal is to deliver therapeutics that will interact with the cells DNA, breaking out of the endosome is critical.
As a natural defence mechanism, bacteria such as Corynebacterium diphtheriae producea protein-based toxin that enters surrounding cells, eventually killing them. Critically, this toxin is known to be capable of escaping from endosomes, which led to the idea of re-engineering it as a delivery platform.
Melnyks lab specializes in bacterial toxins and invented a non-toxic version of the diphtheria toxin, known as attenuated diphtheria toxin. This new molecule has the capacity to enter the cell and efficiently escape the endosome and thus excels as a delivery vehicle without any of the toxic effects of diphtheria toxin.
To prove that the concept would work, the researchers used the system to deliver molecules that they believed would be effective against glioblastoma, a form of brain cancer.
Glioblastoma is a highly invasive disease and patients have a very short life expectancy after initial diagnosis, says Shoichet. We want to change this and have thus pursued the delivery of gene therapeutics to treat glioblastoma.
The group first targeted glioblastoma neural stem cells, which are thought to be resistant to chemotherapeutics. Specifically, the researchers focused on delivering silencing RNA (siRNA) against two genes: integrin beta 1 (ITGB1), which is associated with the highly invasive nature of glioblastoma (and other cancers), and eukaryotic translation initiation factor 3 sub-unit b (eIF-3b), which is an essential survival gene. By eliminating this invasive trait, the researchers could potentially limit progression in diseases like cancer.
ITGB1 is involved in cancer cell migration, which contributes to glioblastomas invasion into healthy brain tissues, saysLaura Smith, a senior PhD student on the publication. We used an innovative three-dimensional culture system to significantly reduce cell invasion after treatment with our siRNA-attenuated diphtheria toxin system, which suggests that it may be effective in slowing disease progression.
To demonstrate the breadth of this platform, the researchers also delivered a different nucleic sequence that knocks down eIF-3b, which participates in the survival pathway of cancer cells.
We treated the cells with the attenuated diphtheria toxin-siRNA against eIF-3b and observed downregulation at genetic and phenotypic levels, saysAmy E. Arnold, a recent PhD graduate from the Shoichet lab and first author on the paper.
The group is planning on using this delivery vehicle to treat other diseases in the future.
We recognize the strength of this platform strategy and are actively testing it for the delivery of RNA and other cargoes, Shoichet says.
The research received support from the Canadian Institutes of Health Research and the Natural Sciences and Engineering Research Council of Canada, among others.
Go here to read the rest:
U of T researchers use diphtheria toxin to target genes in cancer cells - News@UofT
Recommendation and review posted by G. Smith
