Teen Discovers Promising Cystic Fibrosis Treatment

A 16-year-old from the Toronto area used a supercomputer system to find a new drug combination that shows potential in treating the genetic disorder cystic fibrosis, and won top honors for his work.
Marshall Zhang, an 11th-grade student at Richmond Hill's Bayview Secondary School, received first place Tuesday in the 2011 Sanofi-Aventis BioTalent Challenge, a contest in which students conduct their own research projects with the help of mentors.

Cystic fibrosis is a potentially fatal condition caused by a genetic mutation, or error. It causes thick, sticky mucus to build up in the lungs and elsewhere. Cystic fibrosis occurs most among white people of northern European ancestry, in about 1 out of 3,000 live births. In the past, most people with cystic fibrosis died in their teens, according to the Mayo Clinic. It has no cure. [10 Worst Hereditary Conditions]

At his mentor's lab, Zhang used the Canadian SCINET supercomputing network to investigate how two promising new compounds acted against the defective protein responsible for the condition. Using computer simulations, he figured out how each of these drugs acted against the protein and discovered they acted on the protein in different spots, raising the possibility they could be used simultaneously without interfering with each other.

Zhang then tested his theory in living cells, and the results exceeded his expectations.
"They actually worked together in creating an effect that was greater than the sum of its parts," he told LiveScience.

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