Scientists from Trinity College Dublin have uncovered a new class of
compounds - glyconaphthalimides - that can be used to target cancer
cells with greater specificity than current options allow.
Cancer is difficult to treat, and many current therapies are unable to specifically target cancer cells.
This is problematic for medical professionals and patients, because it
limits the dose of the drug that can be safely administered, and often
causes severe and debilitating side-effects.
But the Trinity scientists have now demonstrated that a class of
naturally occurring enzymes—glycosidases—that are heavily overexpressed
in tumour tissue can be used to trigger the release of therapeutic payloads only in the local tumour sites where they are needed.
This finding may therefore result in the development of improved
targeted cancer therapies with significantly reduced side-effects for
patients.
In addition to killing cancer cells, the technology may also be used
to image cancer cells, with potential applications in cancer imaging and
diagnosis.
Associate Professor in Chemistry at Trinity, Eoin Scanlan, led the
multidisciplinary group. He said: "This is a really exciting discovery
because it brings us closer to more targeted treatment of cancer. Some
current therapies are limited due to the toxicity of the compounds, but
our compounds are completely inactive until they are released by the
enzymes that are naturally overexpressed at the tumour site. The active
compound is then rapidly taken up by cancer cells."
"Our next steps will be to apply this technology to release specific
anti-cancer drugs and to test it against a range of different cancer
types."
SOURCE:
MedicalXpress and Provided by
Trinity College Dublin



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