TIME

THE CRISPR PIONEERS

THEIR BREAKTHROUGH WORK COULD CHANGE THE WORLD

DR. CARL JUNE’S LAB AT THE UNIVERSITY OF PENNSYLVANIA looks like any other biology research hub. There are tidy rows of black-topped workbenches flanked by shelves bearing boxes of pipettes and test tubes. There’s ad hoc signage marking the different workstations. And there are postdocs buzzing around, calibrating scales, checking incubators and smearing solutions and samples onto small glass slides.

Appearances aside, what June is attempting to do here, on the eighth floor of the glass-encased Smilow Center for Translational Research in Philadelphia, is anything but ordinary. He’s built a career trying to improve the odds for people with intractable end-stage disease, and now, in the university’s brand-new cell-processing lab, he’s preparing to launch his most ambitious study yet: he’s going to try to treat 18 people with stubborn cancers, and he’s going to do it using CRISPR, the most controversial new tool in medicine.

Developed just four short years ago by two groups—Jennifer Doudna, a molecular and cell biologist at the University of California, Berkeley, together with Emmanuelle Charpentier, now at the Max Planck Institute in Berlin; and Feng Zhang, a biomedical engineer at the Broad Institute of Harvard and MIT—CRISPR allows scientists to easily and inexpensively find and alter virtually any piece of DNA in any species. In 2016 alone it was used to edit the genes of vegetables, sheep, mosquitoes and all kinds of cell samples in labs. Now, even as some scientists call for patience and extreme

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