Researchers report that they’ve engineered a common laboratory plant to produce the starting material for a potent chemotherapy drug originally harvested from an endangered Himalayan plant. The new work could ensure an abundant supply of the anticancer drug and make it easier for chemists to tweak the compound to come up with safer and more effective versions.
Throughout history, people have relied on plants for medicines. Even modern drugmakers get about half their new drugs from plants. But that’s harder to do when plants are slow growing and endangered, as is the Himalayan mayapple (Podophyllum hexandrum). The short, leafy plant was the original source of podophyllotoxin, a cytotoxic compound that’s the starting point for an anticancer drug called Etoposide. The drug has been on the U.S. market since 1983 and is used to treat dozens of different cancers, from lymphoma to lung cancer. Today, podophyllotoxin is mainly harvested from the more common American mayapple. But this plant is also slow growing, producing only small quantities of the compound.
Elizabeth Sattely and her graduate student Warren Lau reasoned that the podophyllotoxin-building proteins were likely themselves only made by the plant in response to an injury. So the pair made tiny punctures in the leaves of healthy Himalayan mayapples, testing them before and after to see which new proteins appeared around the damaged tissue. They discovered 31, which they categorized by probable function. The pair then narrowed the likely candidates for enzymes in podophyllotoxin production by focusing on members of four classes known to carry out the right types of chemical reactions. They then spliced genes for each of these enzymes into bacteria known to infect Nicotiana benthamiana, a fast-growing relative of tobacco that serves as a sort of lab rat of plant biologists. The bacteria readily infect tobacco and insert their genes into the plant tissue. Sattely and Lau inserted numerous combinations of genes for the enzymes they thought might produce their desired compound. As they report, they eventually found a group of 10 enzymes that allowed the plant to make a molecule called (-)-4’–desmethyl-epipodophyllotoxin, a direct precursor to Etoposide and a potent cancer drug in its own right.