Estudio identifica base molecular del dolor causado por droga contra el cáncerContributed by: Anonymous · Views: 2,414
Contributed by: Anonymous · July 20, 2007 @ 07:02 PM MDT · Views: 2,414
Study Identifies Molecular Basis of Pain Caused by Cancer DrugNew Haven, Conn. — Peripheral pain, a side effect of the highly effective cancer drug pa*censored*axel, appears to be caused when the drug binds to a protein and initiates improper calcium signaling, a Yale School of Medicine researcher reports in a study published recently in the Proceedings of the National Academy of Sciences.
Pa*censored*axel, a substance isolated from the pacific yew Taxus brevifolia and approved by the FDA in 1990, has been very successful in treating solid tumors such as breast cancer and ovarian cancer. However, serious side effects limit its effectiveness. Peripheral pain, for instance, becomes worse with continued use of pa*censored*axel and increased dosages lead to persistent and irreversible pain, Ehrlich said.
Neurons isolated from a rat stained to show the distribution of calcium signaling molecules -- green is the channel that lets calcium out of the storage location (the endoplasmic reticulum), blue is the nucleus, red is fibroblasts (not affected by drug).
What the researchers found is a new binding protein for pa*censored*axel—neuronal calcium sensor-1 (NCS-1). When pa*censored*axel binds to NCS-1, it makes the cell more sensitive to normal signals and increases the magnitude and frequency of changes in calcium. Over time, increased calcium levels activate an enzyme, calpain, that degrades proteins, especially NCS-1.
Calcium signals are needed for nerves to be stimulated and to respond, and the loss of NCS-1 makes it more difficult to generate any calcium signals, she said. While the loss of NCS-1 stops the protein interaction that is causing the inappropriate calcium signals, it also decreases the ability to have normal responses.
Ehrlich said the findings will be of interest to basic scientists and clinical investigators since pa*censored*axel is widely used to treat solid tumors.
“Our results will be an important contribution towards the development of more effective cancer therapies with fewer side effects,” she said.
PNAS 104: 11103-11108 (June 20, 2007)
Press Contact: Jacqueline Weaver 203-432-8555
Courtesy: Yale University