Molecular Playground/Taxol
  Paclitaxel is one of the CBI Molecules being studied in the University of Massachusetts Amherst Chemistry-Biology Interface Program at UMass Amherst and on display at the Molecular Playground. Paclitaxel, also called Taxol (Bristol-Myers Squibb), is a plant derived anti-cancer agent that was first isolated from the bark of Pacific yew tree, Taxus brevifolia, in 1971. It is a complex diterpenoid with a bulky, fused ring system as well as a number of hydrophobic substituents. Approved by the FDA in 1992, it is currently being used in the treatment of ovarian, breast and lung cancers. In addition, therapies are being developed for treatment of Alzheimer's and post-heart surgery patients. Molecular Playground Banner: "Paclitaxel (Taxol),a plant-derived natural product to treat cancer" Paclitaxel binding to alpha-beta tubulin (PDB code 1jff).
ProductionOriginally, paclitaxel was produced through the extraction of the drug from the bark of Taxus trees. This process was unsustainable because nearly 40,000 mature trees were required to meet the demands for the drug each year. A semi-synthetic route was developed and utilized for paclitaxel production using Taxol precursors, which can be extracted from the needles of Taxus trees. This process is more sustainable because the Taxus needles can be harvested depending on their seasonal availability without the destruction of the tree, but the process uses harsh, expensive solvents and has a low product yield. In 2004, the production of paclitaxel through plant cell culture was approved by the FDA. This was the first plant cell culture production route approved for the production of a pharmaceutical. Currently, Bristol-Myers Squibb is producing paclitaxel for pharmaceutical use solely through the sustainable plant cell culture process. Plants in their natural environment cannot flee from non-ideal conditions, so they rely on an intricate defense system (i.e., stress response) characterized by the synthesis of secondary products that enhance survivability. During this defense response, energy flux shifts from metabolism conserved across species (i.e., growth) to specialized metabolic pathways that include compounds such as paclitaxel (Taxus spp.) [1] It is produced through an intricate metabolic pathway in response to a 'stress' on the tree. In culture, this stress response can be induced using the compound methyl jasmonate [2]. Methyl jasmonate is a largely conserved activator of specialized metabolic pathways across many plant systems [3] [4] [5]. It has been shown that methyl jasmonate participates in a positive feedback biosynthetic pathway, implying that adding the compound to culture will result in the production of more methyl jasmonate and therefore an increased downstream stress response [6]. DocetaxelDocetaxel (Taxotere, sanofi-aventis) is a semi-synthetic analog of Taxol that was discovered during the search for a more easily produced taxane anti-cancer agent. The hydroxyl group modification on docetaxel leads to an increase in the lipid solubility of the drug. It was first approved by the FDA in 1996 and is currently used in the treatment of breast, stomach and prostate cancer. Currently, Taxotere is produced from paclitaxel precursors which are extracted from Taxus brevifolia, the readily available Wester Yew. Mechanism of actionBoth Taxol and Taxotere bind to cell microtubules, promoting their assembly into bundles and preventing cell mitosis. This eventually leads to the death of the cells. Although the mechanism of action for both drugs is the same, Taxotere has been found to be twice as potent as Taxol.
Molecular Playground Banner: "Docetaxel (Taxotere), an analaog of the plant derived anti-cancer agent paclitaxel"
| ||||||||||||
References
Proteopedia Page Contributors and Editors (what is this?)
Sarah Wilson, Rohan Patil, Elizabeth Cummings, Michal Harel, Lynmarie K Thompson, Alexander Berchansky
