Chinese scientists achieve breakthrough in biosynthesis of anticancer drug paclitaxel

Chinese scientists have broken through the critical technological bottleneck in the biosynthesis of the anticancer drug paclitaxel, paving the way for sustainable biomanufacturing of this medicine.

The study, led by Yan Jianbin, a researcher at the Agricultural Genomics Institute at Shenzhen (AGIS) under the Chinese Academy of Agricultural Sciences (CAAS), was published in the latest issue of the academic journal Science.

Paclitaxel, a natural anti-tumor product with an exceptionally complex and unique molecular structure, is widely used in the clinical treatment of breast cancer, ovarian cancer, lung cancer and other cancers. It is the world's best-selling plant-based anticancer drug and one of the few plant-based drugs capable of controlling the growth of cancer cells, said Yan.

In nature, paclitaxel can only be extracted from the rare and endangered gymnosperm of the Taxus genus of plants. A Taxus plant grows very slowly, usually taking decades or even hundreds of years to become a big tree. In addition, the content levels of paclitaxel-like substances in Taxus plants are extremely low. All these factors posed great difficulties for the further utilization of paclitaxel, Yan said.

The research team aimed to tackle the challenge of paclitaxel biosynthesis. In 2021, Yan's group mapped out the first high-quality reference genome of Taxus mairei in the world, which provided a genomic blueprint and key candidate genes for decoding the paclitaxel biosynthesis pathway. The relevant research results were published in the journal Nature Plants.

On this basis, the research team further screened and identified the essential candidate genes and successfully discovered the most critical and previously unknown enzyme in the paclitaxel biosynthesis pathway.

The elucidation of the metabolic pathway responsible for the synthesis of paclitaxel had been an unsolved problem for many years. The Chinese research group managed to fill the gaps in the paclitaxel synthesis pathway. Besides constituting a very important contribution to basic science, this development is also significant for opening the way for the more effective and cheaper synthesis of the taxol drug, as well as for the new ability to synthesize many derivatives in search of more potent anticancer drugs, said Gregory Stephanopoulos, a professor at the Massachusetts Institute of Technology in the United States.

"This finding is a major breakthrough in our understanding of the biosynthesis of complex natural products," said Jens Nielsen, a professor at the Chalmers University of Technology in Sweden. "And it will enable our abilities to produce other valuable natural products at scale and thereby develop new and valuable medicines."