Here’s
good news, possibly wonderful news from ScienceDaily.com: “…a Northwestern
University research team is the first to demonstrate delivery of a drug that
turns off a critical gene in this complex cancer, increasing survival rates
significantly in animals with the deadly disease.” Here’s a link to the web
posting about the success to date in mice: http://www.sciencedaily.com/releases/2013/10/131030142813.htm
What’s
particularly nifty about this protocol is that “The novel therapeutic, which is
based on nanotechnology, is small and nimble enough to cross the blood-brain
barrier and get to where it is needed -- the brain tumor. Designed to target a
specific cancer-causing gene in cells, the drug simply flips the switch of the
troublesome oncogene to "off," silencing the gene. This knocks out
the proteins that keep cancer cells immortal.”
What
I like about this approach is that it seems to bode well for addressing other
diseases: "This is a beautiful marriage of a new technology with the genes
of a terrible disease," said Chad A. Mirkin, a nanomedicine expert and a
senior co-author of the study. "Using highly adaptable spherical nucleic
acids, we specifically targeted a gene associated with GBM and turned it off in
vivo. This proof-of-concept further establishes a broad platform for treating a
wide range of diseases, from lung and colon cancers to rheumatoid arthritis and
psoriasis”.
Appropriately,
the article notes that “Thanks to the Human Genome Project and genomics
research over the last two decades, there is an enormous number of genetic
targets; having the right therapeutic agents and delivery materials has been
the challenge.”
Image
credit: <a
href='http://www.123rf.com/photo_11486779_vector-seamless-dna.html'>happyroman
/ 123RF Stock Photo</a>
1 comment:
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