Fast forward a bit, and now the human genome has been entirely sequenced, and the cost of sequencing has gone down from millions to 10-20k. Not something the average Joe can afford, but more palatable for investors and research firms. Because of this the new fad is personalized medicine, and finding drugs and cures through sequencing. How do you do it you say?
Here's an example. Joe has cancer. He goes to his doctor and they sequence his DNA - once for normal tissue, and once for cancer tissue (FYI double the cost at least). Lab tech crunches the data and finds where the mutations are, and more techs come and discuss which ones may be affecting which pathways to cause the cancer. Drugs are then developed to suppress said genes, and the cancer is controlled. This is very ideal and many things can affect this though. #1 cancer constantly mutates/evolves, so once you control it, it may just mutate and render your old drugs useless. Then you get into the cycle of just testing/drug making/mutating. Sounds expensive.
What scientists are doing now is trying to some data mining. Basically sequence everything - every patient with every type of cancer with every type of background to be ready for whatever comes up. Huge gaps right now though are testing (doh!), and the fact that they really have no idea if the cancer will mutate in predictable ways depending on what drug you use to fight it.
All in all, nice concept - we will have to see how it shakes out, but seems too ideal and expensive (aka not practical). It is though one of the best options for fighting cancer
No comments:
Post a Comment