Drug discovery: Playing dirty
10/14/2005 Simon Frantz [email protected] Forget drugs carefully designed to hit one particular molecule — a better way of treating complex diseases such as cancer may be to aim for several targets at once, says Simon Frantz. It's not often that a science lecture can turn a person on to the idea of promiscuity. But when Michael Heinrich heard a talk about a promising new cancer drug, it triggered a transformation of his ideas about how to target disease. It sounds heretical, but Heinrich and others are now saying that 'magic bullet' drugs designed to hit single biological targets might not be the answer to treating complex illnesses such as cancer and cardiovascular disease. The future, they say, could be in drugs that are less picky about their molecular partners. Heinrich's turning point was a seminar given in early 1998 at the Oregon Health and Science University Cancer Institute in Portland, where he worked. Brian Druker, a molecular biologist in the medical department at the same university, was talking about the revolutionary leukaemia treatment Gleevec (imatinib mesylate). Made by Swiss drug company Novartis, Gleevec was designed to zero in on a single protein in cancerous cells, specifically killing them while leaving healthy cells unharmed. It proved to be spectacularly effective and non-toxic. Compared with the relatively indiscriminate action and distressing side effects of conventional cancer treatments, Gleevec seemed to vindicate the single-target approach to drug discovery. But it soon became clear that Gleevec was not as specific as its creators had [...]