While this headline my seem
a like an oxymoron, it's really good news. As noted in doctortipster.com, “A targeted
molecular therapy has been used successfully by researchers from Cincinnati
Children’s Hospital Medical Center to treat nerve tumours that appear in people
with neurofibromatosis type 1.”
The article reports that “Nancy
Ratner, PhD, principal investigator and the program leader for the Cancer
Biology and Neural tumors Program, said it is the first time researchers could
reduce the size of neurofibromas with a molecularly targeted therapy.”
For me, just reading about neurofibromas
is scary. The article in doctortipster.com says that “neurofibromatosis type 1
is a genetic disorder that is manifested by hyperpigmented skin spots and
tumors of the nervous system. Patients with neurofibromatosis type 1 have cafe
au lait spots, neurofibromas, speech disorders, epilepsy, optic nerve glioma,
bone disorders and others. The disease is progressive, some signs appear at
birth while others appear with age.”
Here’s a link to the
doctortipster.com article - http://www.doctortipster.com/12287-targeted-molecular-therapy-for-untreatable-nf1-tumors.html#ixzz2EwoXnozj
And for those of you that
can read and understand dense scientific-speak, here’s a link to the research
article in the Journal of Clinical
Investigation: http://www.jci.org/articles/view/60578
No comments:
Post a Comment