Linda pretending to be snookered on our Norwegian cruise, 2004
Sometimes I think that the name for this blog ought to be “The
Murine Chronicles”, not “Myrl’sBlog”. Sure,
it is written by Myrl, but much of the time it’s about things we humans do to
mice and rats. This posting is strong to
rats.
There is a gene known as RAS
which is complicit in many kinds of cancer.
When not mutated it produces a protein (RAS), which serves as a signal
within cells, telling them when not to divide.
If mutated, RAS can’t do its
job and the cell multiplies like sin to produce, in some cases, cancer. RAS, therefore,
is a “proto-onco gene”, one of the worst.
Clearly, if we could develop a drug to prevent screwed-up RAS proteins
from doing damage, we’d be way ahead.
Oh, maybe here is where I should tell you where the name RAS
comes from. Rat sarcoma. RAS was discovered by abusing our friend, the
brown rat.
Well, all this has been common knowledge for more than a
decade, and majestic piles of money, effort – and rats – have been expended on
developing a drug to counter the malign effect of mutated RAS, to little
effect. Odd though it seems, drugs like
this work by “binding” to the subject bad-acting molecule. Binding requires a precise shape; your missile
of death has to fit precisely into some irregularity on the surface of its
target. And not just any old
irregularity; as I understand it, it should be the misshapen hole that is
causing the trouble!
Hell, I am in way over my head. Read this link; it is short, relatively easy to
understand, and informative.
https://directorsblog.nih.gov/2018/02/13/kras-targeted-cancer-strategy-shows-early-promise/
And thank God for your little murine friends.
And thank God for your little murine friends.
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